| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs28684 | snp | C/G | 0.32153 | 0.239548 | intron-variant | LASP1 | GRCh38.p7 | 17:38873760 | TGCCAGCCCCACCCT[C/G]GCCGGGGCACCAGCC | 3927 |
| rs82974 | snp | A/G | 0.4231 | 0.180378 | intron-variant | LASP1 | GRCh38.p7 | 17:38908689 | TGGACAGAGTCTGGG[A/G]GGAGTCCAGTCTGGA | 3927 |
| rs82976 | snp | C/T | 0.185788 | 0.241613 | intron-variant | LASP1 | GRCh38.p7 | 17:38908420 | CCACTCTCTTAGTGA[C/T]CCCTGTCCACTGGTG | 3927 |
| rs82977 | snp | A/G | 0.191775 | 0.243125 | intron-variant | LASP1 | GRCh38.p7 | 17:38908095 | CCCTGTCACCCCATC[A/G]CTAATGCAGATAGCG | 3927 |
| rs112901 | snp | A/C | 0.454544 | 0.143743 | intron-variant | LASP1 | GRCh38.p7 | 17:38892000 | ctcagctcaagtgat[A/C]ctcccgcctcaaact | 3927 |
| rs170492 | snp | C/G | 0.366266 | 0.221319 | intron-variant | LASP1 | GRCh38.p7 | 17:38881518 | GGCAGGAAGAAAACA[C/G]GAGGAGGCTGGGCTA | 3927 |
| rs226212 | snp | C/T | 0.446902 | 0.154045 | intron-variant | LASP1 | GRCh38.p7 | 17:38880301 | ATGAGGCTGATAAAA[C/T]GCAGAGAAAACAAGG | 3927 |
| rs226213 | snp | A/G | 0.172351 | 0.237636 | intron-variant | LASP1 | GRCh38.p7 | 17:38880235 | ACTGAATTCTAGGCT[A/G]CTTGAGTCACTGGGC | 3927 |
| rs226214 | snp | C/T | 0.337614 | 0.234145 | intron-variant | LASP1 | GRCh38.p7 | 17:38879926 | GCTGCAACCCTTCCT[C/T]TACCCAGATAACCTG | 3927 |
| rs226215 | snp | C/G | 0.361894 | 0.223562 | intron-variant | LASP1 | GRCh38.p7 | 17:38878565 | CAAATACAACAGACA[C/G]GTCACTCATTCTTGA | 3927 |
| rs226216 | snp | A/C | 0.451359 | 0.148171 | intron-variant | LASP1 | GRCh38.p7 | 17:38877743 | CCTGCCCAGAGCTGG[A/C]GAGGCCTCATTGCTT | 3927 |
| rs226217 | snp | C/T | 0.296873 | 0.245566 | intron-variant | LASP1 | GRCh38.p7 | 17:38876048 | AAGCCCAGGATGATG[C/T]GCTGGATCACCACCA | 3927 |
| rs226218 | snp | A/T | 0.499995 | 0.00159744 | intron-variant | LASP1 | GRCh38.p7 | 17:38875090 | CCATGACCCACTTTC[A/T]CACACACACACACAC | 3927 |
| rs226219 | snp | A/G | 0.299411 | 0.245069 | intron-variant | LASP1 | GRCh38.p7 | 17:38874518 | AAGGCCCCAAGGTTC[A/G]AGAAAACCCACCAGC | 3927 |
| rs226220 | snp | C/T | 0.202959 | 0.245534 | intron-variant | LASP1 | GRCh38.p7 | 17:38874390 | CTAAGATGAAAGAAC[C/T]CCTGCCTTGTCTCAA | 3927 |
| rs226221 | snp | A/G | 0.272241 | 0.249009 | intron-variant | LASP1 | GRCh38.p7 | 17:38873424 | GCTACCTGAGCCTCC[A/G]TTTATGGAGTGCATC | 3927 |
| rs226222 | snp | C/T | 0.154661 | 0.231107 | intron-variant | LASP1 | GRCh38.p7 | 17:38885144 | ACCTCCAGCACTCAG[C/T]TCTGGGGAAAGATGT | 3927 |
| rs226223 | snp | C/T | 0.466308 | 0.125343 | intron-variant | LASP1 | GRCh38.p7 | 17:38884610 | TTGAGGTCAGGAGTT[C/T]GACACCAGCCTGGAC | 3927 |
| rs226224 | snp | C/T | 0.418007 | 0.185132 | intron-variant | LASP1 | GRCh38.p7 | 17:38909484 | gagtagctgggatta[C/T]aggcaactgccacca | 3927 |
| rs226225 | snp | A/G | 0.385168 | 0.210309 | intron-variant | LASP1 | GRCh38.p7 | 17:38909435 | atttttagtagagac[A/G]ggcttttaccatgtt | 3927 |
| rs226226 | snp | A/G | 0.420096 | 0.183214 | intron-variant | LASP1 | GRCh38.p7 | 17:38909424 | agacaggcttttacc[A/G]tgttggccaggctgg | 3927 |
| rs226227 | snp | C/T | 0.416708 | 0.186302 | intron-variant | LASP1 | GRCh38.p7 | 17:38909262 | AGAAAGGTGTGAGGG[C/T]TCAGGGTTTGAGTGC | 3927 |
| rs226228 | snp | A/G | 0.42263 | 0.180829 | intron-variant | LASP1 | GRCh38.p7 | 17:38908755 | CTGGCTGAACAGCCA[A/G]TAGTTCCTGCAGCCC | 3927 |
| rs226229 | snp | G/T | 0.402454 | 0.198136 | intron-variant | LASP1 | GRCh38.p7 | 17:38907218 | AAAGTGAGGCTCAGC[G/T]CCTTCCAGCCTGGGC | 3927 |
| rs226230 | snp | A/G | 0.34659 | 0.230587 | intron-variant | LASP1 | GRCh38.p7 | 17:38892926 | CTGGCCCTCAGTGAG[A/G]CCCTAATGAAGAGTG | 3927 |
| rs226231 | snp | C/T | 0.312348 | 0.242101 | intron-variant | LASP1 | GRCh38.p7 | 17:38892513 | CCAGCACCTCTTCTC[C/T]GAGGTCCTTCTGAGC | 3927 |
| rs226232 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | LASP1 | GRCh38.p7 | 17:38892172 | GGGTCTTTTACCTTC[C/T]CCCAGAACCCAGTCA | 3927 |
| rs226233 | snp | A/G | 0.467337 | 0.123551 | intron-variant | LASP1 | GRCh38.p7 | 17:38889647 | ctatatacctcatac[A/G]catggcctgaaggta | 3927 |
| rs226234 | snp | C/T | 0.030278 | 0.119257 | intron-variant | LASP1 | GRCh38.p7 | 17:38888924 | TTCTTCAGTTCATGC[C/T]GAACTTAGCCGCCAA | 3927 |
| rs226235 | snp | A/G | 0.395818 | 0.203069 | intron-variant | LASP1 | GRCh38.p7 | 17:38887776 | GGAGACCTCAATCAA[A/G]GGAGCATAACTTGAC | 3927 |
| rs226236 | snp | C/T | 0.394354 | 0.204112 | intron-variant | LASP1 | GRCh38.p7 | 17:38887418 | TTCCAGGCCAAGGGA[C/T]GATCAACCACGAGTC | 3927 |
| rs523120 | snp | C/T | 0.405082 | 0.196086 | intron-variant, upstream-variant-2KB | LASP1, MIR6779 | GRCh38.p7 | 17:38914741 | TCTTGGGAAGCAGTC[C/T]TTTCCTCGCCTGCAT | 3927 |
| rs523145 | snp | A/T | 0.432651 | 0.170701 | intron-variant, upstream-variant-2KB | LASP1, MIR6779 | GRCh38.p7 | 17:38914735 | GAAGCAGTCTTTTCC[A/T]CGCCTGCATGCGTGC | 3927 |
| rs525767 | snp | C/T | 0.459137 | 0.136973 | intron-variant, upstream-variant-2KB | LASP1, MIR6779 | GRCh38.p7 | 17:38914484 | TGCACCAACAGGACC[C/T]GCACTCACCCGGGGC | 3927 |
| rs525989 | snp | C/T | 0.458229 | 0.13837 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | LASP1, MIR6779 | GRCh38.p7 | 17:38914405 | GCTGCTGCCGTCCTG[C/T]GAATCCCGACGCTCT | 3927 |
| rs530253 | snp | A/G | 0.441158 | 0.161117 | intron-variant | LASP1 | GRCh38.p7 | 17:38911109 | GTCTCCCACAGCACT[A/G]CACACCCCAGGCCTC | 3927 |
| rs533075 | snp | A/G | 0.442113 | 0.159977 | intron-variant | LASP1 | GRCh38.p7 | 17:38910808 | TTGAACCTTGGAGGC[A/G]GAGGTCGCAGTGAGC | 3927 |
| rs559586 | snp | C/T | 0.476227 | 0.106402 | intron-variant | LASP1 | GRCh38.p7 | 17:38910197 | TTTGCCAAAATATTC[C/T]GACGGCATACTCCTA | 3927 |
| rs569502 | snp | A/G | 0.4087 | 0.193169 | intron-variant | LASP1 | GRCh38.p7 | 17:38915742 | GCCTGATCTCACCCC[A/G]TTCCTGCTGGGCTTA | 3927 |
| rs598751 | snp | C/T | 0.246485 | 0.249975 | intron-variant | LASP1 | GRCh38.p7 | 17:38917279 | TATGGGATAAGAAGT[C/T]ACACCTCCCATGAAG | 3927 |
| rs600158 | snp | C/T | 0.307423 | 0.243316 | intron-variant | LASP1 | GRCh38.p7 | 17:38916929 | cctgtcctcgttgca[C/T]ggctcactccttcct | 3927 |
| rs608420 | snp | C/T | 0.404384 | 0.196635 | intron-variant | LASP1 | GRCh38.p7 | 17:38891032 | TCCTACAGGGGCACA[C/T]ACCTCCCACTCAGCA | 3927 |
| rs638366 | snp | A/G | 0.396 | 0.202938 | intron-variant | LASP1 | GRCh38.p7 | 17:38910571 | TGCTCTAGACCACCC[A/G]TTCTCAGACTTGAAG | 3927 |
| rs640306 | snp | C/T | 0.440057 | 0.162414 | intron-variant | LASP1 | GRCh38.p7 | 17:38911008 | gattacaggcgtgag[C/T]caccgcgcccggcca | 3927 |
| rs646097 | snp | C/T | 0.369592 | 0.21954 | utr-variant-3-prime, nc-transcript-variant | LASP1 | GRCh38.p7 | 17:38920078 | TTGGTGGGCTTCCTC[C/T]ACTCAGAGATGGGGG | 3927 |
| rs653342 | snp | A/G | 0.399432 | 0.200425 | intron-variant | LASP1 | GRCh38.p7 | 17:38911586 | TGAGGGAGTGGGCTG[A/G]GAGAGTCACTTCTGG | 3927 |
| rs654660 | snp | C/T | 0.441021 | 0.161279 | intron-variant | LASP1 | GRCh38.p7 | 17:38911875 | CTTGGCTCACCGCAA[C/T]CTCTGCCTCCCAGGT | 3927 |
| rs655565 | snp | C/T | 0.440746 | 0.161604 | intron-variant | LASP1 | GRCh38.p7 | 17:38912103 | ACACCACAAGAAAGG[C/T]GGGTGGTGAggccga | 3927 |
| rs656027 | snp | C/G | 0.412583 | 0.189912 | intron-variant | LASP1 | GRCh38.p7 | 17:38912207 | GACCTTGACTTTTCC[C/G]CTGTCCCATATGGGC | 3927 |
| rs660413 | snp | C/T | 0.29432 | 0.24604 | utr-variant-3-prime, nc-transcript-variant | LASP1 | GRCh38.p7 | 17:38919253 | CCCATCCCACTGGTC[C/T]CTACACAGCGGCAGA | 3927 |
| rs676107 | snp | A/G | 0.286825 | 0.247273 | intron-variant | LASP1 | GRCh38.p7 | 17:38918015 | gtagctgggactata[A/G]gcgtgtaccaccatg | 3927 |
| rs683234 | snp | A/G | 0.441432 | 0.160792 | intron-variant | LASP1 | GRCh38.p7 | 17:38912238 | CCAGGGGCCGGTTCT[A/G]GGCTGGCCCAGGTGG | 3927 |
| rs685098 | snp | G/T | 0.41408 | 0.188621 | intron-variant | LASP1 | GRCh38.p7 | 17:38912682 | GAAGGTGCCATGGGG[G/T]ATGGGAGGTGGAGGA | 3927 |
| rs687255 | snp | A/G | 0.449599 | 0.150533 | intron-variant, upstream-variant-2KB | LASP1, MIR6779 | GRCh38.p7 | 17:38913141 | ACAACATGAGGCCCA[A/G]CTCAAGACTCCTGGG | 3927 |
| rs741018 | snp | A/G | 0.454904 | 0.143228 | intron-variant | LASP1 | GRCh38.p7 | 17:38908545 | TGTTCCTGAGGTGAG[A/G]CAGCCAACCCTGGCC | 3927 |
| rs741021 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | LASP1 | GRCh38.p7 | 17:38907872 | TAGAGCTGGTCAGGG[C/T]TTGCAGGACCGCCTG | 3927 |
| rs758967 | snp | A/C | 0.239614 | 0.249784 | intron-variant | LASP1 | GRCh38.p7 | 17:38890903 | TGGAGGTTTGGGACG[A/C]GGCTATAGAGGGTTG | 3927 |
| rs979607 | snp | C/T | 0.487368 | 0.0784625 | upstream-variant-2KB | LASP1 | GRCh38.p7 | 17:38868066 | CTTGACTATGAAAAC[C/T]AGGAGAAGTAATCCA | 3927 |
| rs1005654 | snp | A/T | 0.328148 | 0.237472 | intron-variant | LASP1 | GRCh38.p7 | 17:38911228 | AACCCAGGGCTTCCA[A/T]AGCACCTGGGACTGG | 3927 |
| rs1038651 | snp | C/T | 0.304688 | 0.243945 | intron-variant, nc-transcript-variant | LASP1 | GRCh38.p7 | 17:38896912 | TACAGATGAAGAAAC[C/T]GAGGCCAGGGGCTTG | 3927 |
| rs1049495 | snp | C/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | LASP1 | GRCh38.p7 | 17:38921680 | CGGGATCAAACCTTT[C/T]TGGCCTGTTATGATT | 3927 |
| rs1063331 | snp | C/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | LASP1 | GRCh38.p7 | 17:38918784 | GGCCATCTGAACCCG[C/G]AGCGCCCCCATCTGT | 3927 |
| rs1063332 | snp | C/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | LASP1 | GRCh38.p7 | 17:38918841 | CCGTCCTGGGCGTGA[C/G]CCGTCCATTCTTCAG | 3927 |
| rs1063333 | snp | G/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | LASP1 | GRCh38.p7 | 17:38918977 | TGGCAGGCTTCCCCC[G/T]TGATCGACTTCTTGG | 3927 |
| rs1076438 | snp | C/T | 0.435263 | 0.167862 | intron-variant | LASP1 | GRCh38.p7 | 17:38907874 | GAGCTGGTCAGGGTT[C/T]GCAGGACCGCCTGGG | 3927 |
| rs1130638 | snp | C/T | 0.446687 | 0.154319 | synonymous-codon, nc-transcript-variant | LASP1 | GRCh38.p7 | 17:38898519 | GGACCAGATCAGTAA[C/T]GTGAGCTCTTGCCCT | 3927 |
| rs1352431 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | LASP1 | GRCh38.p7 | 17:38872148 | TGGTGAATACTGAGG[C/G]CTAGAGACATTCATA | 3927 |
| rs1873050 | snp | A/G | 0.495056 | 0.049474 | intron-variant | LASP1 | GRCh38.p7 | 17:38872816 | GCCTTTGGGAGATAA[A/G]GCTCAGGGAGGAGAA | 3927 |
| rs1962810 | snp | C/T | 0.0498117 | 0.149749 | utr-variant-5-prime, nc-transcript-variant | LASP1 | GRCh38.p7 | 17:38869884 | GGCCCGCGGTGCTGG[C/T]GCCTCAGCGCTCTCA | 3927 |
| rs1982815 | snp | C/T | 0.495252 | 0.0484902 | intron-variant | LASP1 | GRCh38.p7 | 17:38903881 | CATCATTAAAGGCAT[C/T]TGAAGAGTTGCCTTT | 3927 |
| rs2004052 | snp | A/G | 0.366679 | 0.221102 | upstream-variant-2KB | LASP1 | GRCh38.p7 | 17:38869201 | GACTAAAAAAAAAAA[A/G]AAAAAGAAAAGAAAA | 3927 |
| rs2004053 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | LASP1 | GRCh38.p7 | 17:38869197 | aaaaaaaaaaaaaaa[A/G]aaaaaagaaaaaGTA | 3927 |
| rs2029345 | snp | A/G | 0.498009 | 0.0314867 | intron-variant | LASP1 | GRCh38.p7 | 17:38894322 | CACCTTGATGGGGTC[A/G]TGGGAAATTACAGGG | 3927 |
| rs2058431 | snp | A/T | 0.484632 | 0.086302 | intron-variant | LASP1 | GRCh38.p7 | 17:38894740 | AAAAAAATACAAATT[A/T]AAAAAAAAAATTAGA | 3927 |
| rs2087294 | snp | C/T | 0.366679 | 0.221102 | upstream-variant-2KB | LASP1 | GRCh38.p7 | 17:38869195 | GATACTTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 3927 |
| rs2241009 | snp | A/G | 0.457676 | 0.139228 | intron-variant, upstream-variant-2KB | LASP1, MIR6779 | GRCh38.p7 | 17:38914936 | CCCCGCCCCCAACCT[A/G]GCTCAAGCCCCACAG | 3927 |
| rs2241010 | snp | A/G | 0.432944 | 0.170387 | utr-variant-5-prime, nc-transcript-variant | LASP1 | GRCh38.p7 | 17:38869886 | GGGGCCCGCGGTGCT[A/G]GCGCCTCAGCGCTCT | 3927 |
| rs2286883 | snp | C/T | 0.480107 | 0.0977277 | intron-variant | LASP1 | GRCh38.p7 | 17:38898631 | CCTGGAGGGCAGGGG[C/T]AGTGGAGGCACTGGC | 3927 |
| rs2302471 | snp | C/T | | | intron-variant, upstream-variant-2KB | LASP1, MIR6779 | GRCh38.p7 | 17:38914495 | CTCAGGTCATCTGCA[C/T]CAACAGGACCCGCAC | 3927 |
| rs2338371 | snp | C/G | 0 | 0 | intron-variant, upstream-variant-2KB | LASP1, MIR6779 | GRCh38.p7 | 17:38914055 | TCTGATTCTTCAGTT[C/G]TCATGGTCCTtttac | 3927 |
| rs2338372 | snp | A/C/T | 0 | 0 | splice-acceptor-variant, upstream-variant-2KB | LASP1, MIR6779 | GRCh38.p7 | 17:38914324 | CTCATGGTATTTTAT[A/C/T]TGCAAGGTCAGAAGG | 3927 |
| rs3220064 | microsatellite | (CA)15/16/17/24/25/26 | 0.496392 | 0.256564 | intron-variant | LASP1 | GRCh38.p7 | 17:38875058 | CATGACCCACTTTCT[(CA)15/16/17/24/25/26]CGAAGGGCTACACAC | 3927 |
| rs3744075 | snp | C/T | 0.129078 | 0.21881 | synonymous-codon, nc-transcript-variant | LASP1 | GRCh38.p7 | 17:38918679 | GGACGGGGACACCAT[C/T]GTCAACGTGCAGCAG | 3927 |
| rs3760152 | snp | A/G | 0.185472 | 0.241529 | upstream-variant-2KB | LASP1 | GRCh38.p7 | 17:38868587 | TGTCCCCATCTTTAG[A/G]TTATGAAACTCCATG | 3927 |
| rs3785461 | snp | A/G | 0.44768 | 0.153045 | intron-variant | LASP1 | GRCh38.p7 | 17:38885753 | CACCCATGTTGGCAT[A/G]CACACATTTCCAGCC | 3927 |
| rs3785462 | snp | A/G | 0.495999 | 0.0445491 | intron-variant | LASP1 | GRCh38.p7 | 17:38892863 | GCTTCCCAGGGTCAT[A/G]GCCTGCTGGGTTCCC | 3927 |
| rs3785464 | snp | A/C | 0.204803 | 0.245881 | intron-variant | LASP1 | GRCh38.p7 | 17:38896548 | GCCATGGCGATTATT[A/C]CCCTGGATTAGGGGC | 3927 |
| rs3785465 | snp | A/G | 0.445724 | 0.155538 | intron-variant | LASP1 | GRCh38.p7 | 17:38900982 | AGTGGGGGAGGGGGA[A/G]GATGGTCTTAGATTA | 3927 |
| rs3785466 | snp | C/T | 0.289683 | 0.24683 | intron-variant | LASP1 | GRCh38.p7 | 17:38903491 | CAACCTCCTGAGTAG[C/T]TGGTACTACAGGCAT | 3927 |
| rs3785467 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | LASP1 | GRCh38.p7 | 17:38908196 | CCTGCTGGCACCTTC[A/G]GGGCCCAGGGCAGGC | 3927 |
| rs3785471 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant, upstream-variant-2KB | LASP1, MIR6779 | GRCh38.p7 | 17:38913312 | TTTTGGAACCTGACC[C/T]GAGAAGGAGCCCATC | 3927 |
| rs3826294 | snp | C/T | 0.197082 | 0.244335 | intron-variant | LASP1 | GRCh38.p7 | 17:38871731 | CTTGGGGAGTGTGGG[C/T]ATATGGGGCCGCTGC | 3927 |
| rs3837797 | in-del | -/GTTTACCT | | | intron-variant | LASP1 | GRCh38.p7 | 17:38874009 | TGCCCCTACCAGCCT[-/GTTTACCT]TTCTTTAGAGTGGGT | 3927 |
| rs3837798 | in-del | -/C | 0.387074 | 0.209071 | intron-variant | LASP1 | GRCh38.p7 | 17:38885643 | GCACCCAGCTGATCA[-/C]CCTGTCCCTCATTCC | 3927 |
| rs3837799 | in-del | -/T | | | intron-variant | LASP1 | GRCh38.p7 | 17:38893014 | GTGTGTGTGTGTGTG[-/T]CAAGCATGCACGCAT | 3927 |
| rs3837800 | in-del | -/T | 0.439918 | 0.162576 | intron-variant | LASP1 | GRCh38.p7 | 17:38911444 | GGATATGACATTGAC[-/T]TACCTCAGAGACTTG | 3927 |
| rs3842366 | in-del | -/A | 0.0221141 | 0.102801 | upstream-variant-2KB | LASP1 | GRCh38.p7 | 17:38869275 | TTAACAAGGGGAAGG[-/A]AAAAACCAAGCCATT | 3927 |
| rs3842367 | in-del | -/GGCCCTGGCGCAG | | | intron-variant, upstream-variant-2KB | LASP1, MIR6779 | GRCh38.p7 | 17:38913609 | TAAAACACCTAGCAC[-/GGCCCTGGCGCAG]TAAGAGCTCAGGAAA | 3927 |
| rs3889067 | snp | A/G | 0 | 0 | upstream-variant-2KB | LASP1 | GRCh38.p7 | 17:38869196 | AAAAAAAAAAAAAAA[A/G]GAAAAGAAAAAGTAT | 3927 |
| rs4042644 | snp | C/G/T | | | intron-variant | LASP1 | GRCh38.p7 | 17:38874229 | TGAGGCCCAGGAATG[C/G/T]TTCGCTGAAATCATC | 3927 |