| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs12967 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | KDM5B | GRCh38.p7 | 1:202728675 | GGCACTGGAAGTGAG[C/T]TGGACTCTTAAGCTG | 10765 |
| rs1141108 | snp | C/T | 0.384765 | 0.210567 | synonymous-codon | KDM5B | GRCh38.p7 | 1:202746156 | TTCCTGTCCTCCTTA[C/T]AAATATAAATTGCGG | 10765 |
| rs1141109 | snp | C/G | 0.385568 | 0.21047 | synonymous-codon | KDM5B | GRCh38.p7 | 1:202736327 | AGGCCGATCTATCCC[C/G]GTACATCTGAATTCT | 10765 |
| rs1892163 | snp | A/G | 0.442206 | 0.159865 | | | GRCh38.p7 | 1:202748900 | TAAAAATTTTACTAA[A/G]TAATACCCAATGACA | 10765 |
| rs1892164 | snp | A/G | 0.442812 | 0.159134 | | | GRCh38.p7 | 1:202749074 | GCAGATCATCTCATC[A/G]TGGGAAAACACACAA | 10765 |
| rs2275891 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | KDM5B, PCAT6 | GRCh38.p7 | 1:202810300 | AAGAATTATCGTCGA[C/T]GGCTCTTTGGTGCGC | 10765 |
| rs2275892 | snp | A/G | 0.120674 | 0.21395 | upstream-variant-2KB | KDM5B, PCAT6 | GRCh38.p7 | 1:202810310 | GTCGATGGCTCTTTG[A/G]TGCGCATTCTGGGCC | 10765 |
| rs2275893 | snp | A/C | 0.120674 | 0.21395 | upstream-variant-2KB | KDM5B, PCAT6 | GRCh38.p7 | 1:202810313 | GATGGCTCTTTGGTG[A/C]GCATTCTGGGCCTCC | 10765 |
| rs2362916 | snp | C/T | 0.138886 | 0.22395 | intron-variant | KDM5B | GRCh38.p7 | 1:202794722 | ACAATAGAAATGTAG[C/T]ATATGgtagtcccca | 10765 |
| rs2363762 | snp | A/T | 0.386694 | 0.20932 | intron-variant | KDM5B | GRCh38.p7 | 1:202768775 | CAGGCTGGAGTGCAA[A/T]GGTGCAATCTCGGCT | 10765 |
| rs2363763 | snp | A/G | 0.282895 | 0.247826 | intron-variant | KDM5B | GRCh38.p7 | 1:202768819 | ACCTCCCAGGTTCAA[A/G]CAATTCTCCTGCCTC | 10765 |
| rs2363960 | snp | C/G | 0.480223 | 0.0974544 | intron-variant | KDM5B | GRCh38.p7 | 1:202801167 | CTTTTGTGTATGCTT[C/G]ACATTTTTTGTAATA | 10765 |
| rs2363965 | snp | C/T | 0.462024 | 0.134014 | intron-variant | KDM5B | GRCh38.p7 | 1:202747003 | AACCCTTCTTGGATA[C/T]ACCTTTTGTCATTTA | 10765 |
| rs2885651 | snp | C/T | 0.499382 | 0.017561 | intron-variant | KDM5B | GRCh38.p7 | 1:202783784 | acaccattctcctac[C/T]tcagtctcctgagta | 10765 |
| rs2885898 | snp | A/G | 0.462363 | 0.131916 | intron-variant | KDM5B | GRCh38.p7 | 1:202761028 | GACCCTGTCTCAGGA[A/G]AAAAAAAAAAAAGAT | 10765 |
| rs3185399 | snp | C/T | 0 | 0 | utr-variant-3-prime | KDM5B | GRCh38.p7 | 1:202728046 | CATTAGGGGATTCTT[C/T]TTTTGTGTCCTGCTC | 10765 |
| rs3196669 | snp | A/G | 0.387599 | 0.208726 | synonymous-codon | KDM5B | GRCh38.p7 | 1:202764110 | ACCCGAGGAGACAAC[A/G]GAAGCCAGAACTCAT | 10765 |
| rs3216061 | in-del | -/A | 0.386059 | 0.210068 | intron-variant | KDM5B | GRCh38.p7 | 1:202746116 | ACTGTTTTCCATAGG[-/A]AAAAAAAATCGTTCT | 10765 |
| rs3795600 | snp | A/G | 0.251578 | 0.249995 | intron-variant | KDM5B | GRCh38.p7 | 1:202741192 | GACCTGAGTAAAAGA[A/G]TGTTAATTTTTTCTT | 10765 |
| rs3820153 | snp | A/G | 0.461037 | 0.134028 | intron-variant | KDM5B | GRCh38.p7 | 1:202756158 | ATCTGAAGGCAAAGG[A/G]TGATAAGTAATTTTC | 10765 |
| rs3935652 | snp | A/G | 0.255503 | 0.249939 | intron-variant | KDM5B | GRCh38.p7 | 1:202730550 | AGAATTTCATTTTTC[A/G]TGGCAAATTTCATTT | 10765 |
| rs3952364 | snp | G/T | 0.461148 | 0.133852 | intron-variant | KDM5B | GRCh38.p7 | 1:202743519 | GTTACTAGAGCACAG[G/T]AGACTCAGAGACAAT | 10765 |
| rs4021241 | in-del | -/GGG | | | intron-variant | KDM5B | GRCh38.p7 | 1:202760212 | ccagctacgtggggg[-/GGG]ctgaggtgggagaac | 10765 |
| rs4245700 | snp | C/G | 0.461148 | 0.133852 | intron-variant | KDM5B | GRCh38.p7 | 1:202754613 | GGGGTATCCAGGCTA[C/G]CACTGCCACCAAATG | 10765 |
| rs4245711 | snp | C/T | 0.499437 | 0.0167637 | intron-variant | KDM5B | GRCh38.p7 | 1:202772138 | GTTATTCTCTTCCTA[C/T]CTCTCTACAGCACAG | 10765 |
| rs4245713 | snp | A/G | 0.362941 | 0.223034 | utr-variant-5-prime, upstream-variant-2KB | KDM5B, PCAT6 | GRCh38.p7 | 1:202809133 | AGACTTGAGAGGGGC[A/G]AAAGACTTGAAATAA | 10765 |
| rs4310498 | snp | A/G | 0.304576 | 0.24397 | intron-variant | KDM5B | GRCh38.p7 | 1:202733925 | GATGATGTCCGAGAT[A/G]GCTTGGCCTTCCCCT | 10765 |
| rs4325196 | snp | A/G | 0.387074 | 0.209071 | intron-variant | KDM5B | GRCh38.p7 | 1:202735732 | ACATGCAACCCTGAG[A/G]CTCTCCTTTACAAAA | 10765 |
| rs4333896 | snp | A/G | 0.386884 | 0.209196 | intron-variant | KDM5B | GRCh38.p7 | 1:202770664 | ACTATTCAATGATAC[A/G]GCAAATGCTCATATG | 10765 |
| rs4348778 | snp | C/T | 0.499776 | 0.0105807 | utr-variant-3-prime, downstream-variant-500B | KDM5B | GRCh38.p7 | 1:202727119 | GGGGTAGGGGTTGTG[C/T]TTACTAAGATGGCAA | 10765 |
| rs4351714 | snp | C/T | 0.498982 | 0.0225409 | intron-variant | KDM5B | GRCh38.p7 | 1:202791530 | TGACCCTCATTCTCA[C/T]TCTACACACCTATTT | 10765 |
| rs4478871 | snp | C/G | 0.387263 | 0.208947 | intron-variant | KDM5B | GRCh38.p7 | 1:202754042 | TTTCCTAAAGCAACC[C/G]ACAAGGGTAAGGCAA | 10765 |
| rs4553255 | snp | C/T | 0.441705 | 0.160466 | intron-variant | KDM5B | GRCh38.p7 | 1:202804974 | TATTCCTATCAAAAT[C/T]TGGGAGACAAAAAAG | 10765 |
| rs4559568 | snp | C/T | 0.37955 | 0.213815 | intron-variant | KDM5B | GRCh38.p7 | 1:202806806 | GAAGGGGTCTTCCTC[C/T]ACTTAGAAGTGGGGG | 10765 |
| rs4950741 | snp | C/T | 0.461037 | 0.134028 | intron-variant | KDM5B | GRCh38.p7 | 1:202737033 | ACCCTTCTAAATTCA[C/T]TCATCTCATTGGTTC | 10765 |
| rs4950742 | snp | A/G | 0.499187 | 0.0201513 | intron-variant | KDM5B | GRCh38.p7 | 1:202753149 | ATATTTTTCAGACTC[A/G]GCTTTGTAAGACTAC | 10765 |
| rs4950791 | snp | C/T | 0.410061 | 0.192043 | intron-variant | KDM5B | GRCh38.p7 | 1:202733225 | TAGGAGCAGAGGAAA[C/T]TAAAAGAATATGTTA | 10765 |
| rs4950792 | snp | A/G | 0.461037 | 0.134028 | intron-variant | KDM5B | GRCh38.p7 | 1:202737544 | AGGTCATCCAGATAT[A/G]TCTCCTGTTGTGATG | 10765 |
| rs4950793 | snp | A/G | 0.382666 | 0.211895 | intron-variant | KDM5B | GRCh38.p7 | 1:202753220 | ATGTGAATGTGAGCC[A/G]GGTGCTGTGGCTCAC | 10765 |
| rs4950878 | snp | A/G | 0.460252 | 0.135255 | intron-variant | KDM5B | GRCh38.p7 | 1:202806373 | CCTAGCATGTGACAT[A/G]AAGCTACATTACTAC | 10765 |
| rs4950912 | snp | A/G | 0.499451 | 0.0165644 | intron-variant | KDM5B | GRCh38.p7 | 1:202797915 | TTAGGGACAGGCCGG[A/G]CATAGTGGCTTGTGC | 10765 |
| rs4950918 | snp | A/G | 0.498964 | 0.02274 | intron-variant | KDM5B | GRCh38.p7 | 1:202805368 | GCTGCCATATACAAA[A/G]TAATGTAAGTACTCT | 10765 |
| rs4950919 | snp | C/T | 0.479502 | 0.0991411 | intron-variant | KDM5B | GRCh38.p7 | 1:202805378 | ACAAAATAATGTAAG[C/T]ACTCTAAGTTTTCAG | 10765 |
| rs4950923 | snp | A/G | 0.460925 | 0.134204 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | KDM5B | GRCh38.p7 | 1:202807320 | TTCGGGAGCGCGGGC[A/G]GGCATCGGGGCCCAC | 10765 |
| rs4950945 | snp | A/T | 0.284995 | 0.247539 | intron-variant | KDM5B | GRCh38.p7 | 1:202776260 | TTTAATTGACTTTTT[A/T]AAAAAATTTAATTCA | 10765 |
| rs4950946 | snp | A/C | 0.499902 | 0.00698814 | intron-variant | KDM5B | GRCh38.p7 | 1:202776301 | CGTGACAGACAAAGA[A/C]TTAAACACTCAGTAA | 10765 |
| rs4950952 | snp | A/G | 0.440609 | 0.161766 | intron-variant | KDM5B | GRCh38.p7 | 1:202770474 | ATTCTTCTCTCCCTA[A/G]TAACTATTTCAAAAA | 10765 |
| rs5780125 | in-del | -/A | 0.210605 | 0.246877 | intron-variant | KDM5B | GRCh38.p7 | 1:202769731 | CCCAACAATTGAGAG[-/A]AAAAAATATTCTGTT | 10765 |
| rs6427963 | snp | C/G | 0.375 | 0.216506 | intron-variant | KDM5B | GRCh38.p7 | 1:202739562 | caatagtggagggaa[C/G]gtcagcagataaaca | 10765 |
| rs6427964 | snp | A/G | 0.382473 | 0.212016 | intron-variant | KDM5B | GRCh38.p7 | 1:202759778 | attaacagtggttat[A/G]tatgcattgtgaaag | 10765 |
| rs6427965 | snp | G/T | 0.385359 | 0.210185 | intron-variant | KDM5B | GRCh38.p7 | 1:202795966 | GAGGCCACAGAGCTG[G/T]AATGGGCCTGACCAG | 10765 |
| rs6427966 | snp | A/G | 0.404035 | 0.196909 | intron-variant | KDM5B | GRCh38.p7 | 1:202796114 | GTCACCTCCTTCCTC[A/G]TGACACCCCTGGACA | 10765 |
| rs6427967 | snp | C/T | 0.479904 | 0.0982045 | intron-variant | KDM5B | GRCh38.p7 | 1:202796151 | AAGGTCCATTTGCAG[C/T]CTCAGTGCCCGCTGG | 10765 |
| rs6427968 | snp | A/T | 0.209084 | 0.246629 | intron-variant | KDM5B | GRCh38.p7 | 1:202801496 | GTCCTAGAGACATCT[A/T]TTCTTCATTAATCTG | 10765 |
| rs6656784 | snp | A/T | 0.499741 | 0.0113788 | intron-variant | KDM5B | GRCh38.p7 | 1:202787476 | aaaaatGAGTTAATC[A/T]CTTTAATCTGTAATg | 10765 |
| rs6658451 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | KDM5B | GRCh38.p7 | 1:202742222 | TTTCCCCTCTGTGGA[C/T]CTACTATAATCTCTT | 10765 |
| rs6668689 | snp | G/T | 0.461259 | 0.133677 | intron-variant | KDM5B | GRCh38.p7 | 1:202775094 | taacaaaaatcagcc[G/T]agtgtggtggcgcgt | 10765 |
| rs6673669 | snp | A/C | | | intron-variant | KDM5B | GRCh38.p7 | 1:202743628 | CTGAAAGAGAAatgg[A/C]ctggtacaaaaacag | 10765 |
| rs6677515 | snp | A/C/T | 0.293533 | 0.278987 | intron-variant | KDM5B | GRCh38.p7 | 1:202802537 | AGCTGGGATTGCAGG[A/C/T]GCCTGCCACCATGCC | 10765 |
| rs6680902 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KDM5B | GRCh38.p7 | 1:202794301 | ATTATGTGGGCTTGA[C/T]AGGGATTTGTTCTTT | 10765 |
| rs6680991 | snp | C/T | 0.49931 | 0.0185575 | intron-variant | KDM5B | GRCh38.p7 | 1:202759532 | CTCCAGCCTGGGTGA[C/T]AGAGTGAGATCCTGT | 10765 |
| rs6686266 | snp | C/T | 0.209997 | 0.246779 | intron-variant | KDM5B | GRCh38.p7 | 1:202779912 | TACATTAGGAATGTA[C/T]GATTATTATGGTATT | 10765 |
| rs6699000 | snp | C/T | 0.106633 | 0.204807 | upstream-variant-2KB | KDM5B, PCAT6 | GRCh38.p7 | 1:202810032 | GGAAAGAGTTCACAG[C/T]GGTCCTGGGAGAACG | 10765 |
| rs7367771 | snp | A/G | 0.49917 | 0.0203505 | intron-variant | KDM5B | GRCh38.p7 | 1:202760778 | ATGCATACCAAATCT[A/G]AAGTGGAATCTCCTA | 10765 |
| rs7411479 | snp | A/G | 0 | 0 | intron-variant | KDM5B | GRCh38.p7 | 1:202796919 | GTGACATCCCTGGAT[A/G]CGGACTCTACCTGGT | 10765 |
| rs7415722 | snp | C/T | 0.387263 | 0.208947 | intron-variant | KDM5B | GRCh38.p7 | 1:202760102 | AGGACTATTTGAGCT[C/T]AGGAGTTCGAGACCA | 10765 |
| rs7519148 | snp | A/G | 0.440746 | 0.161604 | intron-variant | KDM5B | GRCh38.p7 | 1:202765451 | ATGTCCACTGCTAAA[A/G]GAGTTTATTCCATGG | 10765 |
| rs7519619 | snp | C/T | 0.387263 | 0.208947 | intron-variant | KDM5B | GRCh38.p7 | 1:202749460 | TACTCTGGAGGCTGA[C/T]GTGGAAGGATTGCTT | 10765 |
| rs7521277 | snp | A/G | 0.209997 | 0.246779 | intron-variant | KDM5B | GRCh38.p7 | 1:202771196 | GGTTCCACATTCAAC[A/G]TTCTATTTTTTATtt | 10765 |
| rs7526150 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KDM5B | GRCh38.p7 | 1:202751573 | TGACTCTGCCAAACA[C/T]GTGATAATTTATCAG | 10765 |
| rs7527112 | snp | C/T | 0.387263 | 0.208947 | intron-variant | KDM5B | GRCh38.p7 | 1:202755787 | TGAGGGCATAGTGCT[C/T]GTCCTGAAAGAGGAA | 10765 |
| rs7527702 | snp | C/T | 0.387263 | 0.208947 | intron-variant | KDM5B | GRCh38.p7 | 1:202776738 | GGCTAATTTTTTAAA[C/T]TATGTTTTAGCAGAG | 10765 |
| rs7528426 | snp | A/C | 0.209997 | 0.246779 | intron-variant | KDM5B | GRCh38.p7 | 1:202766751 | TTCGATTCCTTACCC[A/C]TTTGATGGTACAATT | 10765 |
| rs7529105 | snp | A/C | 0.461259 | 0.133677 | intron-variant | KDM5B | GRCh38.p7 | 1:202761476 | TAAGGGGACATGGTT[A/C]AGAAGTTCCCCTAAT | 10765 |
| rs7530414 | snp | A/T | 0.21875 | 0.248039 | intron-variant | KDM5B | GRCh38.p7 | 1:202749670 | AATTAAAAAGTGGTT[A/T]AAAAAAAAAAAAAGA | 10765 |
| rs7540914 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | KDM5B | GRCh38.p7 | 1:202740352 | gggtggccggccggg[C/T]ggggggctgaccccc | 10765 |
| rs7541374 | snp | A/T | 0.441021 | 0.161279 | intron-variant | KDM5B | GRCh38.p7 | 1:202761775 | CCCAGCCTATACAAC[A/T]GTGAAAAAATAAATT | 10765 |
| rs7541392 | snp | A/G | 0.209997 | 0.246779 | intron-variant | KDM5B | GRCh38.p7 | 1:202770767 | ATAGCCGTGAGAGAA[A/G]TAACAGGTGGAAGGA | 10765 |
| rs7541444 | snp | C/T | 0.441021 | 0.161279 | intron-variant | KDM5B | GRCh38.p7 | 1:202761798 | AATAAATTTCTGTTG[C/T]TTAAGCCACTCAGTC | 10765 |
| rs7545667 | snp | C/T | 0.5 | 0 | intron-variant | KDM5B | GRCh38.p7 | 1:202787556 | actgggttttaattt[C/T]ttctccaatcaggtg | 10765 |
| rs7546307 | snp | A/G | 0.209997 | 0.246779 | intron-variant | KDM5B | GRCh38.p7 | 1:202747190 | GCCAACAAAGATGAG[A/G]AAGGTAAGGAAAATG | 10765 |
| rs7548747 | snp | A/C | 0.132066 | 0.220435 | intron-variant | KDM5B | GRCh38.p7 | 1:202754946 | catcttggcctccca[A/C]actgctgggattaca | 10765 |
| rs7550852 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KDM5B | GRCh38.p7 | 1:202766831 | ACAAGGTTCAAAACT[A/G]CAAAGAGCACACACA | 10765 |
| rs7551390 | snp | A/G | 0.386694 | 0.20932 | intron-variant | KDM5B | GRCh38.p7 | 1:202761407 | tatgattgtgtcact[A/G]tactccagccATCTC | 10765 |
| rs7551814 | snp | A/T | 0.0364509 | 0.129988 | intron-variant | KDM5B | GRCh38.p7 | 1:202731703 | TTTTGCAAATACATA[A/T]TAGCCTATATCCTAC | 10765 |
| rs7552255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KDM5B | GRCh38.p7 | 1:202780745 | ACTAGAACAAAAACA[C/T]GTAttaggttggtgc | 10765 |
| rs7553104 | snp | G/T | 0.46137 | 0.133501 | intron-variant | KDM5B | GRCh38.p7 | 1:202749707 | ATATTAACAATGTAT[G/T]AGTATCTACAACAAT | 10765 |
| rs7553366 | snp | C/T | 0.463234 | 0.130503 | intron-variant | KDM5B | GRCh38.p7 | 1:202765130 | ATGTCATAACTCCAT[C/T]AGCCTCTAAGAGTTT | 10765 |
| rs7555220 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | KDM5B | GRCh38.p7 | 1:202746521 | TTGTCTAGGGAGATC[C/T]CCTTTTTCAGACAAG | 10765 |
| rs7555841 | snp | A/G | 0.00943375 | 0.0680285 | intron-variant | KDM5B | GRCh38.p7 | 1:202785049 | CTACCTTTTAGGACT[A/G]TGGTGAGAACTGATT | 10765 |
| rs7555856 | snp | C/T | 0 | 0 | intron-variant | KDM5B | GRCh38.p7 | 1:202785212 | GACCTCTAAACCTTA[C/T]TTACCTTTAAGGACC | 10765 |
| rs7555858 | snp | C/T | 0 | 0 | intron-variant | KDM5B | GRCh38.p7 | 1:202785216 | TCTAAACCTTACTTA[C/T]CTTTAAGGACCTTAT | 10765 |
| rs7555870 | snp | C/T | 0 | 0 | intron-variant | KDM5B | GRCh38.p7 | 1:202785251 | CCAGCCTAACCCTAG[C/T]TGGCATGTAACTGTC | 10765 |
| rs9633345 | snp | A/G | 0.40386 | 0.197046 | intron-variant | KDM5B | GRCh38.p7 | 1:202774237 | CACACATCTCAAAAA[A/G]TAAGTTTATTTGTTC | 10765 |
| rs9660046 | snp | A/T | 0.132751 | 0.2208 | intron-variant | KDM5B | GRCh38.p7 | 1:202771940 | TTCATATAATGTATT[A/T]AAAAAAAAAGTTTTG | 10765 |
| rs9660926 | snp | C/T | 0.132751 | 0.2208 | intron-variant | KDM5B | GRCh38.p7 | 1:202767919 | TTTTTAACAAGTGTT[C/T]GGAATAAAAAAAAAT | 10765 |
| rs9662127 | snp | G/T | | | intron-variant | KDM5B | GRCh38.p7 | 1:202768778 | gctggagtgcaaagg[G/T]gcaatctcggctcac | 10765 |
| rs9803787 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | KDM5B | GRCh38.p7 | 1:202751097 | TTATTACCCCTCAAG[C/T]AGCATCTTCTACCAC | 10765 |
| rs10494836 | snp | C/T | 0.210605 | 0.246877 | utr-variant-3-prime | KDM5B | GRCh38.p7 | 1:202727750 | GAGTCTGGGAATTCA[C/T]AAGTCTCCTCTCAAG | 10765 |
| rs10494837 | snp | A/G | 0.0678174 | 0.1712 | utr-variant-3-prime | KDM5B | GRCh38.p7 | 1:202728207 | TTTAGTGTTATGTTA[A/G]GACGAAGGATTTATT | 10765 |