| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs1377 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | DPF3 | GRCh38.p7 | 14:72663112 | GACCATCCAGCTGTG[C/T]TCTCTCTGCCTCTGG | 8110 |
| rs1381 | snp | C/G | 0 | 0 | intron-variant | DPF3 | GRCh38.p7 | 14:72663063 | GCCCTATTCCTGGCT[C/G]ATCTCTTGCTGCTGA | 8110 |
| rs1383 | snp | A/T | 0.381113 | 0.21286 | intron-variant | DPF3 | GRCh38.p7 | 14:72663057 | TTCCTGGCTGATCTC[A/T]TGCTGCTGAAGTTCA | 8110 |
| rs3327 | snp | C/T | 0.128632 | 0.218563 | intron-variant | DPF3, RGS6 | GRCh38.p7 | 14:72627042 | TCAATTTTTAACACT[C/T]CTTTTTATATAGGGA | 8110 |
| rs3854 | snp | A/G | 0.483199 | 0.0901004 | intron-variant, utr-variant-3-prime | DPF3 | GRCh38.p7 | 14:72662275 | TGCCCCACATTTTAA[A/G]TAAGAAAATAAAGAT | 8110 |
| rs11463 | snp | G/T | 0.482905 | 0.0908579 | intron-variant, utr-variant-3-prime | DPF3 | GRCh38.p7 | 14:72662412 | AAAAAGTGCTGACAT[G/T]GCACAGTATTTTTGT | 8110 |
| rs16455 | in-del | -/GCC | 0.487368 | 0.0784625 | intron-variant | DPF3 | GRCh38.p7 | 14:72638271 | GGCAATGATTCAGCC[-/GCC]TGACCTTCACACACT | 8110 |
| rs720317 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | DPF3 | GRCh38.p7 | 14:72850825 | TGTGTGTGTGTGCGC[A/G]CGCGCATGTGTGTAC | 8110 |
| rs722945 | snp | A/G | 0.47709 | 0.104548 | intron-variant | DPF3 | GRCh38.p7 | 14:72647911 | GAAGTGGTACTGTCC[A/G]TGGACTGGAGCTCCT | 8110 |
| rs740080 | snp | G/T | 0.0707826 | 0.174302 | intron-variant | DPF3 | GRCh38.p7 | 14:72651693 | CTTGTTACCCCATTT[G/T]AAGGCTACAGACATC | 8110 |
| rs740081 | snp | A/G | 0.475437 | 0.108066 | intron-variant | DPF3 | GRCh38.p7 | 14:72651513 | CTGTCTTCCTGACTT[A/G]CCTCCATTGCCCAAA | 8110 |
| rs740971 | snp | A/G | 0.417034 | 0.18601 | intron-variant | DPF3 | GRCh38.p7 | 14:72721459 | AGGAAGTCCAAGCTC[A/G]AAAGTCTCCTTTAAT | 8110 |
| rs740972 | snp | C/T | 0.415891 | 0.18703 | intron-variant | DPF3 | GRCh38.p7 | 14:72721441 | GGAGTTCACCAAAGG[C/T]CCAGGAAGTCCAAGC | 8110 |
| rs740973 | snp | C/G | 0.429837 | 0.173662 | intron-variant | DPF3 | GRCh38.p7 | 14:72721396 | GTGAGAGAAGGAAAG[C/G]AAGTGGGTCTGGACA | 8110 |
| rs740974 | snp | A/G | 0.418653 | 0.184544 | intron-variant | DPF3 | GRCh38.p7 | 14:72721366 | ATTTCCCACACTTGC[A/G]TCAGTTTGGTTGGGG | 8110 |
| rs740975 | snp | G/T | 0.444931 | 0.15653 | intron-variant | DPF3 | GRCh38.p7 | 14:72798501 | CAGCTCTCTTTGGAT[G/T]GAGCAATAGTTTTCT | 8110 |
| rs740976 | snp | C/T | 0.277867 | 0.248442 | intron-variant | DPF3 | GRCh38.p7 | 14:72789209 | CACTGTCCCGCCCAC[C/T]GTCAGGGCCATCTGG | 8110 |
| rs740977 | snp | A/G | 0.046775 | 0.145601 | intron-variant | DPF3 | GRCh38.p7 | 14:72789045 | CGAATAAGTAGCCAC[A/G]CCATTATTGGAGGGA | 8110 |
| rs740978 | snp | C/G | 0.0475351 | 0.146656 | intron-variant | DPF3 | GRCh38.p7 | 14:72789009 | CACTGGAGGGCTGGA[C/G]TGGGGATAGGAAGGC | 8110 |
| rs740979 | snp | A/T | 0.230017 | 0.2492 | intron-variant | DPF3 | GRCh38.p7 | 14:72788912 | AGACAAAAATAATCA[A/T]GTCAGTCTGCCCCAA | 8110 |
| rs740980 | snp | A/G | 0.225597 | 0.248806 | intron-variant | DPF3 | GRCh38.p7 | 14:72780070 | TTGGGTAAATGATGA[A/G]TGAATGAGTGAATGA | 8110 |
| rs740981 | snp | C/G | 0.331874 | 0.236213 | intron-variant | DPF3 | GRCh38.p7 | 14:72756014 | CATCTACCACACATG[C/G]ACATGCACGCACACA | 8110 |
| rs747987 | snp | C/T | 0.16846 | 0.236329 | intron-variant | DPF3 | GRCh38.p7 | 14:72798845 | TGGCAACTCCTTCCA[C/T]AATGGCAGAACCAGG | 8110 |
| rs757572 | snp | A/G | 0.497881 | 0.0324789 | intron-variant | DPF3 | GRCh38.p7 | 14:72665321 | GTAATAACAGTATGC[A/G]TGTGACTGCTCAGCA | 8110 |
| rs757655 | snp | A/G | 0.3744 | 0.216852 | intron-variant | DPF3 | GRCh38.p7 | 14:72638287 | GATGTTGGGCTCTGG[A/G]CAATGATTCAGCCGC | 8110 |
| rs758913 | snp | A/G | 0.046775 | 0.145601 | intron-variant | DPF3 | GRCh38.p7 | 14:72797753 | TAGTTTTCGATCACC[A/G]CATCCTACGTTGTAT | 8110 |
| rs758914 | snp | A/T | 0.278664 | 0.248351 | intron-variant | DPF3 | GRCh38.p7 | 14:72781027 | GATCAGCTAGTCTCA[A/T]ATTTCTCAGGATCAC | 8110 |
| rs758915 | snp | C/T | 0.278399 | 0.248382 | intron-variant | DPF3 | GRCh38.p7 | 14:72780832 | GAGAAGGAGCTGGTT[C/T]TCCTGGCATAGGTCT | 8110 |
| rs759283 | snp | G/T | 0.499673 | 0.0127754 | intron-variant | DPF3 | GRCh38.p7 | 14:72889599 | ATATCAGAGGGGAAG[G/T]GGTGGGGGTCACATT | 8110 |
| rs763388 | snp | A/G | 0.471388 | 0.116136 | intron-variant | DPF3 | GRCh38.p7 | 14:72855858 | ATGCCTCAAGCCAAT[A/G]AAAGCCCGAAAGGTA | 8110 |
| rs765247 | snp | A/C | 0.0995161 | 0.199636 | intron-variant | DPF3 | GRCh38.p7 | 14:72725026 | tgagCCCATAAAGAA[A/C]CCCCCAggTggccag | 8110 |
| rs767874 | snp | C/T | 0.0539452 | 0.155121 | intron-variant | DPF3 | GRCh38.p7 | 14:72832588 | AAAGTAAAGTAACCA[C/T]GAACTACAGATAGGG | 8110 |
| rs768840 | snp | C/T | 0.340108 | 0.233197 | intron-variant | DPF3 | GRCh38.p7 | 14:72676749 | GAGGCCTCACAATCA[C/T]GGCAGAAGGCAAAGG | 8110 |
| rs882319 | snp | A/G | 0.303438 | 0.244222 | intron-variant | DPF3 | GRCh38.p7 | 14:72664465 | CATTGTTTCATTTTT[A/G]TGGCCTGCAGTTGAC | 8110 |
| rs917069 | snp | A/G | 0.452473 | 0.146644 | intron-variant | DPF3 | GRCh38.p7 | 14:72648797 | ctggctgaatggtct[A/G]ctagagagagagaga | 8110 |
| rs929328 | snp | C/T | 0.3746 | 0.216737 | utr-variant-3-prime, intron-variant | DPF3, RGS6 | GRCh38.p7 | 14:72611146 | TCCATGTGTGGATGT[C/T]GGCTCAGAGCTATAG | 8110 |
| rs973963 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | DPF3 | GRCh38.p7 | 14:72807665 | GGAATGGATTAGTTC[A/G]CTGGAGAGTTGGTTG | 8110 |
| rs982972 | snp | A/G | 0.482008 | 0.0931261 | intron-variant | DPF3 | GRCh38.p7 | 14:72877007 | CTGAAGGGGCACAAA[A/G]GAAGGAAAGAGTATT | 8110 |
| rs991882 | snp | A/C | 0.171057 | 0.237209 | intron-variant | DPF3, RGS6 | GRCh38.p7 | 14:72625951 | TACTCTAGTTAATTT[A/C]TTTTCATAGGTATAT | 8110 |
| rs994758 | snp | C/T | 0.373598 | 0.21731 | intron-variant | DPF3, RGS6 | GRCh38.p7 | 14:72629963 | TGGGGAATATGGTCT[C/T]AGTGCAAGCAGAATT | 8110 |
| rs994759 | snp | G/T | 0.492727 | 0.0598633 | intron-variant | DPF3, RGS6 | GRCh38.p7 | 14:72629906 | CTTGATCTGAATAAC[G/T]GGGTGGTGAAGAATG | 8110 |
| rs994760 | snp | C/T | 0.0289141 | 0.116709 | intron-variant | DPF3, RGS6 | GRCh38.p7 | 14:72629770 | TGGCAGTTCATACTT[C/T]GGCCCTAATGCTGTT | 8110 |
| rs1004552 | snp | C/T | 0.369346 | 0.219673 | intron-variant | DPF3 | GRCh38.p7 | 14:72831642 | ttggctcagtgctgc[C/T]actgacgggagcata | 8110 |
| rs1035021 | snp | A/C | 0.405776 | 0.195535 | intron-variant | DPF3 | GRCh38.p7 | 14:72726923 | tggggccagcaatgg[A/C]aggagggaaatcagg | 8110 |
| rs1035099 | snp | A/T | 0.311369 | 0.242351 | intron-variant | DPF3 | GRCh38.p7 | 14:72860102 | GGTCAACATCGCAGC[A/T]AAGCTTGTAAAAATT | 8110 |
| rs1060570 | snp | G/T | 0.496172 | 0.0435835 | intron-variant | DPF3 | GRCh38.p7 | 14:72671481 | AATCCCCGTCACCAG[G/T]TGATGCACCGGGTTA | 8110 |
| rs1076431 | snp | G/T | 0.0592355 | 0.161582 | intron-variant | DPF3 | GRCh38.p7 | 14:72788094 | GCACTGTGAAGGGCT[G/T]GGATCATACCCTGTC | 8110 |
| rs1076432 | snp | A/T | 0.20111 | 0.245173 | intron-variant | DPF3 | GRCh38.p7 | 14:72778863 | ATCAATTTCAACTCA[A/T]TTCAATGTTTAGTAT | 8110 |
| rs1106631 | snp | C/T | 0.165527 | 0.235296 | intron-variant | DPF3 | GRCh38.p7 | 14:72787181 | TCCATGCCCTGCTTA[C/T]ACCCCTTTCCTCCCC | 8110 |
| rs1122523 | snp | A/G | 0.187685 | 0.242109 | intron-variant | DPF3 | GRCh38.p7 | 14:72833125 | GTCTTCCTAGCTTTG[A/G]GTTACTTTCATCCAT | 8110 |
| rs1123134 | snp | C/T | 0.156319 | 0.231784 | intron-variant | DPF3 | GRCh38.p7 | 14:72831635 | ATCCAAGTATGCTCC[C/T]GTCAGTAGCAGCACT | 8110 |
| rs1123135 | snp | A/G | 0.233235 | 0.249437 | intron-variant | DPF3 | GRCh38.p7 | 14:72831859 | TGAATCTAAGCAAAG[A/G]GGATATTGGTGTTCA | 8110 |
| rs1126160 | snp | A/C | 0.477937 | 0.102688 | intron-variant | DPF3 | GRCh38.p7 | 14:72802354 | AGCAAACTGGAGCCC[A/C]AAACACTTAGCGATG | 8110 |
| rs1160094 | snp | C/T | 0.388775 | 0.207946 | intron-variant | DPF3 | GRCh38.p7 | 14:72750209 | GGTTGCCTGATTTCC[C/T]TGTTCAATACTTTTT | 8110 |
| rs1468662 | snp | A/G | 0.100588 | 0.200439 | intron-variant | DPF3 | GRCh38.p7 | 14:72817034 | GACTGAGGAGAGACC[A/G]GAGGGATGAGGAATG | 8110 |
| rs1544579 | snp | C/T | 0.4628 | 0.13121 | intron-variant | DPF3 | GRCh38.p7 | 14:72826250 | CCAGGCAGACAGCAG[C/T]CAGCTGCTTTGATGC | 8110 |
| rs1557926 | snp | C/G | 0.412416 | 0.190055 | intron-variant | DPF3 | GRCh38.p7 | 14:72643945 | AAAGGAGCCAGTGAG[C/G]CTTCGTTGGGGTCTC | 8110 |
| rs1860747 | snp | A/G | 0.466721 | 0.124627 | intron-variant | DPF3 | GRCh38.p7 | 14:72843116 | AGAGGAGAGCTCCCC[A/G]GAATGATACATGACA | 8110 |
| rs1860748 | snp | A/C | 0.158962 | 0.232835 | intron-variant | DPF3 | GRCh38.p7 | 14:72843103 | CCGGAATGATACATG[A/C]CAAATAAAATATGGC | 8110 |
| rs1860749 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | DPF3 | GRCh38.p7 | 14:72843071 | CCAAGAGCCTTGTCC[A/G]CTGGATTGCTTTATC | 8110 |
| rs1860750 | snp | A/T | 0.499187 | 0.0201513 | intron-variant | DPF3 | GRCh38.p7 | 14:72843030 | TTTATTTATTTATTT[A/T]TTTTTTTGAGATGGA | 8110 |
| rs1861162 | snp | C/T | 0.423881 | 0.179625 | intron-variant | DPF3 | GRCh38.p7 | 14:72863600 | ATGTGGGCAGACACA[C/T]GTGCCCTTTTCTACA | 8110 |
| rs1986423 | snp | A/G | 0.159951 | 0.233219 | intron-variant | DPF3 | GRCh38.p7 | 14:72696602 | TGGGCGAAGAGGCAA[A/G]TTGCAGAATCTAATC | 8110 |
| rs1989638 | snp | C/T | 0.4087 | 0.193169 | intron-variant | DPF3 | GRCh38.p7 | 14:72649479 | TCCTTCCTTCTTCCT[C/T]TTCTCACTTTGTTGC | 8110 |
| rs1990437 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | DPF3 | GRCh38.p7 | 14:72746900 | GCCTGCCGTAACATG[C/T]GAGGGGAAGGGAAAG | 8110 |
| rs1990438 | snp | A/G | 0.357024 | 0.225933 | intron-variant | DPF3 | GRCh38.p7 | 14:72746492 | CCTACTACTAGGCCT[A/G]CTAAAAACACAGAAA | 8110 |
| rs1990439 | snp | A/G | 0.339656 | 0.233371 | intron-variant | DPF3 | GRCh38.p7 | 14:72742034 | AAGGAGCAGGGACTG[A/G]GGGACGAAGTCTGTG | 8110 |
| rs1990440 | snp | C/G | 0.161924 | 0.233971 | intron-variant | DPF3 | GRCh38.p7 | 14:72810446 | TCTGCAGCCCGGAAG[C/G]TCGGTACACATTTGC | 8110 |
| rs1990441 | snp | G/T | 0.496314 | 0.0427728 | intron-variant | DPF3 | GRCh38.p7 | 14:72810384 | TGATTCACATTCTCC[G/T]CCCGTCTCTTCCTTC | 8110 |
| rs1990442 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | DPF3 | GRCh38.p7 | 14:72810269 | GTTCAGGCACATCAA[C/T]GAGCATGTTCTGAGT | 8110 |
| rs1990443 | snp | A/G | 0.377385 | 0.215112 | intron-variant | DPF3 | GRCh38.p7 | 14:72806207 | ATCTGAGGAAGGATG[A/G]CTAAGAGCTGAGGGG | 8110 |
| rs2021736 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | DPF3 | GRCh38.p7 | 14:72672210 | AACCTGAGTTTTACA[A/G]ATTTCAGGATGCTCT | 8110 |
| rs2023479 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | DPF3 | GRCh38.p7 | 14:72677663 | CCAGGGCATCACTGT[A/G]CCACCCACTAACATC | 8110 |
| rs2023480 | snp | A/T | 0.145305 | 0.227022 | intron-variant | DPF3 | GRCh38.p7 | 14:72665628 | ACAATCTTGTTTTTC[A/T]CAACCTCGATACTGG | 8110 |
| rs2052141 | snp | C/T | 0.440746 | 0.161604 | intron-variant, upstream-variant-2KB | DPF3 | GRCh38.p7 | 14:72795118 | ccccaaagatgtcca[C/T]gtcctaatccttgga | 8110 |
| rs2052142 | snp | A/G | 0.046775 | 0.145601 | intron-variant, utr-variant-5-prime | DPF3 | GRCh38.p7 | 14:72795034 | gttaaggactttgag[A/G]tgaggagattatcct | 8110 |
| rs2052143 | snp | A/G | 0.206336 | 0.246157 | intron-variant, utr-variant-5-prime | DPF3 | GRCh38.p7 | 14:72794933 | agctggagatatgac[A/G]ttggaagtggaggta | 8110 |
| rs2052144 | snp | G/T | 0.378372 | 0.214524 | intron-variant | DPF3 | GRCh38.p7 | 14:72776437 | AGCTCTCAGAGCTGG[G/T]CTGGCTTCTCAATTC | 8110 |
| rs2052145 | snp | G/T | 0.38555 | 0.210062 | intron-variant | DPF3 | GRCh38.p7 | 14:72776404 | ATGGGATCACAGAAG[G/T]ACCTCCATCACTCAC | 8110 |
| rs2052146 | snp | A/C | 0.0998734 | 0.199905 | intron-variant | DPF3 | GRCh38.p7 | 14:72770511 | ttaaacaaacaaaca[A/C]actcacaatcactat | 8110 |
| rs2078435 | snp | C/T | 0.195526 | 0.243993 | intron-variant | DPF3 | GRCh38.p7 | 14:72883887 | TAGGCTGGAGTGCAG[C/T]GGCGTGATCTTGGCT | 8110 |
| rs2079989 | snp | C/T | 0.484632 | 0.086302 | intron-variant | DPF3 | GRCh38.p7 | 14:72777761 | aggcatgtcacatga[C/T]aaaaacaggagcaag | 8110 |
| rs2080252 | snp | A/C | 0.499824 | 0.00938333 | intron-variant | DPF3 | GRCh38.p7 | 14:72875199 | ccaaatctcaacttg[A/C]attgatctcccagaa | 8110 |
| rs2098194 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | DPF3 | GRCh38.p7 | 14:72748810 | tactcacaggctcaa[C/T]accacatggaatttg | 8110 |
| rs2098195 | snp | C/G | 0.107694 | 0.205546 | intron-variant | DPF3 | GRCh38.p7 | 14:72787530 | CTTTCTATGTTCCTG[C/G]TAATGACTTAGTGTG | 8110 |
| rs2107684 | snp | A/G | 0.495891 | 0.0451408 | intron-variant | DPF3 | GRCh38.p7 | 14:72655710 | GTTTATATTCACACT[A/G]AAGCAATGTCTCAAG | 8110 |
| rs2107685 | snp | C/T | 0.16846 | 0.236329 | intron-variant | DPF3 | GRCh38.p7 | 14:72655671 | TGACTTCCATTGTTT[C/T]GGTAGCATGAGCCAC | 8110 |
| rs2107686 | snp | C/T | 0 | 0 | intron-variant | DPF3 | GRCh38.p7 | 14:72655431 | TTTCATAATTGCTCA[C/T]AGGACTTGGATATTA | 8110 |
| rs2107687 | snp | C/T | 0.093417 | 0.194889 | intron-variant | DPF3, RGS6 | GRCh38.p7 | 14:72623908 | TAATATGTAAATATA[C/T]TTATACATTTTATGC | 8110 |
| rs2109791 | snp | G/T | 0.357238 | 0.225832 | intron-variant | DPF3 | GRCh38.p7 | 14:72748998 | taggtggtgccccag[G/T]tgggactctgtgtgg | 8110 |
| rs2109792 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | DPF3 | GRCh38.p7 | 14:72747576 | GGTTGCAAACTCCTG[G/T]CCTCAAGCAATCCTC | 8110 |
| rs2109793 | snp | C/G | 0.450609 | 0.149185 | intron-variant | DPF3 | GRCh38.p7 | 14:72739172 | TCACTGCAACCTCCC[C/G]CTTCCAGGTTCAAGC | 8110 |
| rs2109794 | snp | C/T | 0.444931 | 0.15653 | intron-variant | DPF3 | GRCh38.p7 | 14:72822147 | caggtgatccaccca[C/T]cttggcctcccaaag | 8110 |
| rs2109795 | snp | A/G | 0.095934 | 0.196885 | intron-variant | DPF3 | GRCh38.p7 | 14:72813150 | CCAGAATTTGGAGCC[A/G]AGCCCATCAGGGACA | 8110 |
| rs2110552 | snp | A/G | 0.498437 | 0.0279115 | intron-variant | DPF3 | GRCh38.p7 | 14:72888423 | TTACTGGTGTTTCAC[A/G]GTCTGTCAAACCATA | 8110 |
| rs2159714 | snp | A/G | 0.0988009 | 0.199095 | intron-variant | DPF3 | GRCh38.p7 | 14:72813441 | GTCAGAGTTTGCAAA[A/G]CTTTTGCAGATCCTT | 8110 |
| rs2159715 | snp | A/C | 0.299916 | 0.244966 | intron-variant | DPF3 | GRCh38.p7 | 14:72812944 | TCCCATTGCCCCCAA[A/C]CCCATTCCTATCCCT | 8110 |
| rs2160137 | snp | C/T | 0.37778 | 0.214877 | intron-variant | DPF3 | GRCh38.p7 | 14:72868244 | GTGGGAGGAGAGAGA[C/T]GTCTGACTCCCAGGT | 8110 |
| rs2191821 | snp | A/C | 0.470521 | 0.117772 | intron-variant | DPF3 | GRCh38.p7 | 14:72824322 | CCAGACCAGTCCTGG[A/C]AGCCCCAGTCCAAAC | 8110 |
| rs2191822 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | DPF3 | GRCh38.p7 | 14:72824208 | CCCTGGGGCTGGGCT[C/T]GGGGCAGACATTCCT | 8110 |