SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs2810 | snp | A/G | 0.12932 | 0.218944 | utr-variant-3-prime | AMPH | GRCh38.p7 | 7:38384727 | GTTATTATGCTCTTA[A/G]TGATTTACAGACTGA | 273 |
rs715413 | snp | C/T | 0.471958 | 0.115042 | intron-variant | AMPH | GRCh38.p7 | 7:38394923 | TTAAATACTGAAGTT[C/T]TCAAAACTCTCTTCA | 273 |
rs715414 | snp | C/G | 0.49533 | 0.0480965 | intron-variant | AMPH | GRCh38.p7 | 7:38394764 | TGAAGGCATGAGTGA[C/G]TTTGTCCCCACTCCC | 273 |
rs720667 | snp | C/T | 0.471958 | 0.115042 | intron-variant | AMPH | GRCh38.p7 | 7:38394665 | GTCACACGAAAACCA[C/T]CTTCCTTTTGTTCCC | 273 |
rs720668 | snp | C/T | 0.472052 | 0.11486 | intron-variant | AMPH | GRCh38.p7 | 7:38394673 | AAAACCACCTTCCTT[C/T]TGTTCCCAAACACAG | 273 |
rs722334 | snp | A/G | 0.464936 | 0.127682 | intron-variant | AMPH | GRCh38.p7 | 7:38465425 | ATTGAAGAAATTTTA[A/G]CAAGCAGGACATTAC | 273 |
rs722335 | snp | A/C | 0.495445 | 0.0475058 | intron-variant | AMPH | GRCh38.p7 | 7:38465414 | CTGGTCCACAGATTG[A/C]AGAAATTTTAGCAAG | 273 |
rs722336 | snp | A/C | 0.494733 | 0.0510469 | intron-variant | AMPH | GRCh38.p7 | 7:38465305 | TCACTGAAGGCCAGA[A/C]ATAAATGTAAAAGCA | 273 |
rs723001 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | AMPH | GRCh38.p7 | 7:38448985 | TATATTATGACTAAT[A/T]GTATAAAGGCTGACA | 273 |
rs730582 | snp | A/G | 0.287346 | 0.247195 | intron-variant | AMPH | GRCh38.p7 | 7:38524011 | TTACTAGAGATACCT[A/G]CATATCATCTGTTGA | 273 |
rs740066 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | AMPH | GRCh38.p7 | 7:38455802 | tgagtggctgcagct[C/T]gtaggcattctgagc | 273 |
rs741265 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | AMPH | GRCh38.p7 | 7:38455930 | ctgctaggagaaatc[C/T]tatgcacctctgagg | 273 |
rs749582 | snp | A/G | 0.465752 | 0.246654 | intron-variant | AMPH | GRCh38.p7 | 7:38592815 | ATTGATTAGTGAACC[A/G]AGATGCAGGGAGTCT | 273 |
rs887967 | snp | C/T | 0.333261 | 0.235728 | intron-variant | AMPH | GRCh38.p7 | 7:38438418 | GCAGAGGTAAGACTG[C/T]AGTTGGTACCTCTGA | 273 |
rs891883 | snp | G/T | 0.18134 | 0.240387 | intron-variant | AMPH | GRCh38.p7 | 7:38592257 | agcactgtgacatga[G/T]catgatggccatgac | 273 |
rs891884 | snp | A/G | 0.38934 | 0.207568 | intron-variant | AMPH | GRCh38.p7 | 7:38594477 | CCTCACAGGTTGTTA[A/G]TAGATCACATGGAAT | 273 |
rs893412 | snp | A/C | 0.297636 | 0.24542 | intron-variant | AMPH | GRCh38.p7 | 7:38546623 | CAATATCATCACATT[A/C]TCTTGTTTGCTATTT | 273 |
rs893413 | snp | A/G | 0.499809 | 0.00978247 | intron-variant | AMPH | GRCh38.p7 | 7:38546801 | CTGGAATTGCATTTC[A/G]CTAGCTATTTACACC | 273 |
rs893414 | snp | C/T | 0.235854 | 0.249599 | intron-variant | AMPH | GRCh38.p7 | 7:38547090 | GCAGCCATCTCATCC[C/T]CTTGCCTTTCAGGTG | 273 |
rs893415 | snp | C/T | 0.144632 | 0.226711 | intron-variant | AMPH | GRCh38.p7 | 7:38547215 | TGCCCCTAAATCCCT[C/T]GCTGGTTTCCCATAA | 273 |
rs920268 | snp | A/G | 0.498714 | 0.0253268 | intron-variant | AMPH | GRCh38.p7 | 7:38549032 | gcaagcttccagctt[A/G]cttatctatgttggc | 273 |
rs929629 | snp | C/T | 0.148514 | 0.228474 | intron-variant | AMPH | GRCh38.p7 | 7:38412951 | CCACATGGAAATTTG[C/T]GTTGATGGAGATCTA | 273 |
rs967022 | snp | C/T | 0.39009 | 0.207062 | intron-variant | AMPH | GRCh38.p7 | 7:38519205 | aatgaatttcctttc[C/T]ttataaattacccac | 273 |
rs967025 | snp | C/G | 0.334182 | 0.235401 | intron-variant | AMPH | GRCh38.p7 | 7:38445051 | atatatacatatata[C/G]atggtatatacatat | 273 |
rs973527 | snp | C/T | 0.34437 | 0.231505 | intron-variant | AMPH | GRCh38.p7 | 7:38435150 | CCTAAGAGACCCTTT[C/T]GTTTTTTGCAAAGCA | 273 |
rs973528 | snp | A/G | 0.417521 | 0.185571 | intron-variant | AMPH | GRCh38.p7 | 7:38435280 | TCACATTCTAGAAAA[A/G]AGCATGGACTAGACA | 273 |
rs986284 | snp | C/T | 0.440471 | 0.161928 | intron-variant | AMPH | GRCh38.p7 | 7:38608965 | ATTTATCATTGACTA[C/T]GTAAAGCACGTTCAT | 273 |
rs986826 | snp | A/T | 0.413582 | 0.189052 | intron-variant | AMPH | GRCh38.p7 | 7:38407618 | ATCTAAAATAAAATT[A/T]AAAAATTTTAAATTA | 273 |
rs1014570 | snp | C/T | 0.462909 | 0.131034 | intron-variant | AMPH | GRCh38.p7 | 7:38471187 | ACTATCACTCTGACC[C/T]TGAGTTACATTAGAC | 273 |
rs1014571 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | AMPH | GRCh38.p7 | 7:38471295 | TTCACTAAATGGTGG[C/T]TTTACTTATTTTACA | 273 |
rs1014572 | snp | C/G | 0.463018 | 0.130857 | intron-variant | AMPH | GRCh38.p7 | 7:38471659 | taaatggactgagca[C/G]agcaatcgaaaggca | 273 |
rs1019284 | snp | A/G | 0.0619417 | 0.1651 | intron-variant | AMPH | GRCh38.p7 | 7:38415706 | ACCATTAGGCAAACT[A/G]AATTGCTGTAAACTG | 273 |
rs1019285 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | AMPH | GRCh38.p7 | 7:38415847 | ATTCTTGCATCACCT[A/G]TGGATCTCAGGAAGT | 273 |
rs1019286 | snp | A/G | 0.34659 | 0.230587 | intron-variant | AMPH | GRCh38.p7 | 7:38420751 | TCCAATCCTGAGAGA[A/G]CTAATTTAGTGAGAA | 273 |
rs1019287 | snp | A/G | 0.364401 | 0.222289 | intron-variant | AMPH | GRCh38.p7 | 7:38420946 | GAGCCAAACACTGGG[A/G]CGTTTTCTTGCTCCT | 273 |
rs1019288 | snp | A/C | 0.498568 | 0.0267188 | intron-variant | AMPH | GRCh38.p7 | 7:38463423 | CTAAAATCACCCAGC[A/C]ATTTAGTGAATCTGA | 273 |
rs1019289 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | AMPH | GRCh38.p7 | 7:38467255 | GCAGGCAGTGGGCAA[A/C]CCCTAGATGTGTCTG | 273 |
rs1019290 | snp | C/G | 0.495368 | 0.0478996 | intron-variant | AMPH | GRCh38.p7 | 7:38467289 | TAGGGCAAAGGAGAA[C/G]ACTTGCACCTGTATT | 273 |
rs1030016 | snp | A/C | 0.339656 | 0.233371 | intron-variant | AMPH | GRCh38.p7 | 7:38399972 | TAGGAGTATTGCTAA[A/C]CCGCCTGTCCATCAC | 273 |
rs1030017 | snp | C/T | 0.330947 | 0.236533 | intron-variant | AMPH | GRCh38.p7 | 7:38451268 | ACATATTTATGTGTG[C/T]ATATACATGTATATA | 273 |
rs1030018 | snp | C/T | 0.463018 | 0.130857 | intron-variant | AMPH | GRCh38.p7 | 7:38471633 | CCTACATTTTGGTAA[C/T]TATATAAAGGTAAAT | 273 |
rs1030654 | snp | A/G | 0.310878 | 0.242475 | intron-variant | AMPH | GRCh38.p7 | 7:38583988 | CAAATTCTAAACCCC[A/G]GAAACACATGACCAT | 273 |
rs1058654 | snp | A/G | | | utr-variant-5-prime | AMPH | GRCh38.p7 | 7:38631398 | ctccGCGCCGCCGCC[A/G]GCCCCGCTGCGCGCT | 273 |
rs1058655 | snp | G/T | 0.319853 | 0.240068 | synonymous-codon | AMPH | GRCh38.p7 | 7:38391880 | CACCAGCGAGACACC[G/T]GAGCTGGCTACGGAG | 273 |
rs1058656 | snp | A/G | 0.336445 | 0.234579 | synonymous-codon | AMPH | GRCh38.p7 | 7:38391835 | GGACCCTCAGCCCAC[A/G]CCTTCTGCACCAGCC | 273 |
rs1120005 | snp | G/T | 0.423413 | 0.180077 | intron-variant | AMPH | GRCh38.p7 | 7:38404692 | GACAGCTTCTTCACA[G/T]GAGAAAGAATCAGCA | 273 |
rs1158376 | snp | C/G | 0.321769 | 0.239477 | intron-variant | AMPH | GRCh38.p7 | 7:38422811 | TTTTTGTATAGACAG[C/G]GTTTCATCATGTTGC | 273 |
rs1469654 | snp | G/T | 0.308908 | 0.242961 | intron-variant | AMPH | GRCh38.p7 | 7:38583678 | gggggcaggggctct[G/T]ctttattttctttag | 273 |
rs1540479 | snp | A/T | 0.357877 | 0.225527 | intron-variant | AMPH | GRCh38.p7 | 7:38553519 | ATAGGTTACTGAGGG[A/T]TCACACGTGCCATTT | 273 |
rs1540480 | snp | C/T | 0.494651 | 0.0514399 | intron-variant | AMPH | GRCh38.p7 | 7:38553521 | AGGTTACTGAGGGAT[C/T]ACACGTGCCATTTTA | 273 |
rs1540481 | snp | A/G | 0.473543 | 0.111932 | intron-variant | AMPH | GRCh38.p7 | 7:38554034 | CCCGCAGCCCCAGCT[A/G]CATCGTTTCTGCCAC | 273 |
rs1544636 | snp | A/G | 0.301518 | 0.244634 | intron-variant, synonymous-codon | AMPH | GRCh38.p7 | 7:38428242 | TCATTGCTGAATCCA[A/G]GCTTGGCTGCCAGAT | 273 |
rs1545145 | snp | G/T | 0.149665 | 0.228982 | intron-variant | AMPH | GRCh38.p7 | 7:38502281 | GCCTAGAGACTAAAT[G/T]TACTGTATTTTATTC | 273 |
rs1558617 | snp | A/C | 0.159951 | 0.233219 | intron-variant | AMPH | GRCh38.p7 | 7:38483386 | GTTGCCACAGCCCCT[A/C]CCCTCAACTGAGGGA | 273 |
rs1558618 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | AMPH | GRCh38.p7 | 7:38401640 | ttctgacctttagta[C/T]tgatatggataagtc | 273 |
rs1561308 | snp | A/C | 0.443195 | 0.158668 | intron-variant | AMPH | GRCh38.p7 | 7:38542481 | CCAGATGTTTGAGAG[A/C]AAGCTTACATCTGCC | 273 |
rs1561309 | snp | A/C | 0.303938 | 0.244112 | intron-variant | AMPH | GRCh38.p7 | 7:38545100 | TTCTATAATTTCAAG[A/C]ACCATACATGTGCCA | 273 |
rs1561310 | snp | C/T | 0.143959 | 0.226396 | intron-variant | AMPH | GRCh38.p7 | 7:38545302 | ACCTGTCTTCCTGTA[C/T]AGGAAAATCTGGGCT | 273 |
rs1801448 | snp | A/G | | | synonymous-codon | AMPH | GRCh38.p7 | 7:38391772 | GGAGGCCTCTCAGGA[A/G]TTGCCTCCTGGCTTT | 273 |
rs1861239 | snp | C/T | 0.160938 | 0.233598 | intron-variant | AMPH | GRCh38.p7 | 7:38475984 | GTCAGACTGCTTTAC[C/T]ACTGTGTACCTCACA | 273 |
rs1861240 | snp | G/T | 0.493613 | 0.0561475 | intron-variant | AMPH | GRCh38.p7 | 7:38388032 | gttaaaaattaagaa[G/T]aataaagacattttc | 273 |
rs1864887 | snp | A/G | 0.156319 | 0.231784 | intron-variant | AMPH | GRCh38.p7 | 7:38616461 | ATGAATGATTCATTA[A/G]GGTAGGCCCTCTTTA | 273 |
rs1864888 | snp | A/G | 0.15665 | 0.231917 | intron-variant | AMPH | GRCh38.p7 | 7:38615945 | ATCTTTGGCTCTAGC[A/G]GAGGCCAGTGGCATG | 273 |
rs1963818 | snp | A/C | 0.0596104 | 0.162024 | intron-variant | AMPH | GRCh38.p7 | 7:38400357 | tgctgggattacagg[A/C]atgagccaccgtgcc | 273 |
rs1971809 | snp | C/T | 0.379942 | 0.213577 | intron-variant | AMPH | GRCh38.p7 | 7:38500461 | GCCAGAAAGGCTTAT[C/T]TGATGCTTCACCCAG | 273 |
rs1974673 | snp | G/T | 0.381308 | 0.21274 | intron-variant | AMPH | GRCh38.p7 | 7:38414677 | ATATTGAATTTTTTT[G/T]TTTTTGAGACAGAGT | 273 |
rs1974674 | snp | A/T | 0.381308 | 0.21274 | intron-variant | AMPH | GRCh38.p7 | 7:38414721 | CCTGGTTGGAGTGCA[A/T]TGGTTAAGATCTCAG | 273 |
rs1982179 | snp | A/G | 0.306182 | 0.243605 | intron-variant | AMPH | GRCh38.p7 | 7:38545862 | AAAGGCAATTTCACC[A/G]ATGGTTTCTATATTT | 273 |
rs1986521 | snp | A/T | 0.0655868 | 0.168795 | intron-variant | AMPH | GRCh38.p7 | 7:38558583 | CACCTCCTCCCTCCT[A/T]CCCATCATTATTCCT | 273 |
rs1987195 | snp | A/G | 0.493881 | 0.054972 | intron-variant | AMPH | GRCh38.p7 | 7:38560095 | TTCACCTCTTCATGG[A/G]AGGAGCTGAAGGGTC | 273 |
rs1990585 | snp | A/G | 0.394171 | 0.204242 | intron-variant | AMPH | GRCh38.p7 | 7:38438841 | TAAATGCACATGTAC[A/G]TAATGTCTAGGAAAT | 273 |
rs1990586 | snp | A/G | 0.393619 | 0.204631 | intron-variant | AMPH | GRCh38.p7 | 7:38438846 | GCACATGTACGTAAT[A/G]TCTAGGAAATACTCA | 273 |
rs2004204 | snp | A/T | 0.40733 | 0.194287 | intron-variant | AMPH | GRCh38.p7 | 7:38568879 | CCTTTGGGCAATTCT[A/T]ACATGTTTATAGACC | 273 |
rs2014157 | snp | A/G | 0.492918 | 0.0590819 | intron-variant | AMPH | GRCh38.p7 | 7:38414691 | TTTTTTTGAGACAGA[A/G]TCTCACTCTGTCGCC | 273 |
rs2014872 | snp | A/G | 0.36606 | 0.221428 | intron-variant | AMPH | GRCh38.p7 | 7:38500025 | CCCCCAGACTGGGTA[A/G]TTTATAAAGAAAAAG | 273 |
rs2014874 | snp | G/T | 0.379354 | 0.213933 | intron-variant | AMPH | GRCh38.p7 | 7:38500006 | ATAAAGAAAAAGAGG[G/T]TTAATGGACTCACAG | 273 |
rs2018639 | snp | C/T | 0.497091 | 0.0380279 | intron-variant | AMPH | GRCh38.p7 | 7:38445010 | atatatatatatata[C/T]acacacacacacacg | 273 |
rs2024407 | snp | C/T | 0.278399 | 0.248382 | intron-variant | AMPH | GRCh38.p7 | 7:38396836 | CTCATAGCTTTATTG[C/T]CGGAGACATTAACAG | 273 |
rs2024408 | snp | C/T | 0.499793 | 0.0101816 | intron-variant | AMPH | GRCh38.p7 | 7:38393337 | CATACCATTAAGCCC[C/T]CTCTTAATGTTGCCT | 273 |
rs2028209 | snp | G/T | 0.497984 | 0.0316851 | intron-variant | AMPH | GRCh38.p7 | 7:38512436 | AACCTGGGAATCATT[G/T]AGACAGATGCATCCA | 273 |
rs2028210 | snp | A/G | 0.499703 | 0.0121769 | intron-variant | AMPH | GRCh38.p7 | 7:38494809 | ACTACAATAATCATA[A/G]TGTGTCCTATTACGT | 273 |
rs2043260 | snp | A/G | 0.492484 | 0.0608394 | intron-variant | AMPH | GRCh38.p7 | 7:38617624 | TTAAGTCATCAGTGG[A/G]TGACAGAGCTGCTGG | 273 |
rs2043785 | snp | A/T | 0.417683 | 0.185425 | intron-variant | AMPH | GRCh38.p7 | 7:38490003 | taattttgaaaataa[A/T]ttGCCATGCAATAAA | 273 |
rs2043786 | snp | G/T | 0.43598 | 0.167067 | intron-variant | AMPH | GRCh38.p7 | 7:38490968 | TCAGTTTGAGGACTT[G/T]TAATAATTCTTCTCT | 273 |
rs2043787 | snp | A/G | 0.496583 | 0.0411924 | intron-variant | AMPH | GRCh38.p7 | 7:38505899 | TTTTATTGTCAATCT[A/G]TGCTGCAACTCCCTA | 273 |
rs2043788 | snp | A/C | 0.49655 | 0.04139 | intron-variant | AMPH | GRCh38.p7 | 7:38505907 | TCAATCTATGCTGCA[A/C]CTCCCTACCAGATCT | 273 |
rs2072505 | snp | A/G | 0.308414 | 0.24308 | utr-variant-3-prime | AMPH | GRCh38.p7 | 7:38384438 | ATAAGATAATCTTGT[A/G]CTACAGGATAATTCA | 273 |
rs2072506 | snp | A/T | 0.295088 | 0.245901 | intron-variant | AMPH | GRCh38.p7 | 7:38462795 | ATGTGAGGAAATATC[A/T]AGTCAAATAAGAAAA | 273 |
rs2072507 | snp | C/T | 0.44755 | 0.153212 | intron-variant | AMPH | GRCh38.p7 | 7:38394386 | TATTCATCAACACTC[C/T]GACTTCTCTTCTGCT | 273 |
rs2080286 | snp | C/G | 0.245631 | 0.249962 | intron-variant | AMPH | GRCh38.p7 | 7:38440462 | AACAGAACTATGCAT[C/G]TACACAAAGGAGGAG | 273 |
rs2080287 | snp | A/C | 0.249606 | 0.25 | intron-variant | AMPH | GRCh38.p7 | 7:38440563 | tggctgcttatacaa[A/C]aataataacaaaata | 273 |
rs2083146 | snp | A/C | 0.338069 | 0.233974 | intron-variant | AMPH | GRCh38.p7 | 7:38517832 | tatagccacgtgatc[A/C]tttgttaaagagatt | 273 |
rs2083147 | snp | A/G | 0.344147 | 0.231595 | intron-variant | AMPH | GRCh38.p7 | 7:38531323 | TGGAACTACAGGCAC[A/G]CACCATGGCACCAGG | 273 |
rs2099609 | snp | A/C | 0.0425829 | 0.139564 | intron-variant | AMPH | GRCh38.p7 | 7:38517615 | gtgatgcacaaggat[A/C]tctggtggaagaaat | 273 |
rs2110652 | snp | C/T | 0.278399 | 0.248382 | intron-variant | AMPH | GRCh38.p7 | 7:38402587 | ACATAGAATCACCTG[C/T]TCTGAATCCCCTAAA | 273 |
rs2110653 | snp | A/G | 0.499087 | 0.0213463 | intron-variant | AMPH | GRCh38.p7 | 7:38406204 | caaaacttctgggat[A/G]cagcaacagcaatgc | 273 |
rs2110654 | snp | G/T | 0.172351 | 0.237636 | intron-variant | AMPH | GRCh38.p7 | 7:38447026 | TTACTAttttttttt[G/T]ttgtttgtttgagac | 273 |
rs2116667 | snp | A/G | 0.203882 | 0.245709 | intron-variant | AMPH | GRCh38.p7 | 7:38601152 | TTCTATTACAGAAGG[A/G]CAGGTTTATGGCTGG | 273 |
rs2118457 | snp | A/C/T | 0.021333 | 0.101051 | intron-variant | AMPH | GRCh38.p7 | 7:38531322 | CTGGAACTACAGGCA[A/C/T]GCACCATGGCACCAG | 273 |
rs2118458 | snp | C/T | 0.143959 | 0.226396 | intron-variant | AMPH | GRCh38.p7 | 7:38541930 | AGTGCAGTAAGCACC[C/T]GCCAAGGCTGCTTTC | 273 |