SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs83626 | snp | G/T | 0.34989 | 0.229177 | intron-variant | RAD18 | GRCh38.p7 | 3:8887171 | aagccccttcctaaa[G/T]ctactgaatcagaat | 56852 |
rs124847 | snp | C/T | 0.483708 | 0.088773 | intron-variant | RAD18 | GRCh38.p7 | 3:8886920 | GCTGGGGCCAGAACA[C/T]GAAAAGCCTTGGATG | 56852 |
rs166094 | snp | A/T | 0.498611 | 0.0263212 | intron-variant | RAD18 | GRCh38.p7 | 3:8884640 | TAATTTTTCTTTCCA[A/T]GTTTCCCCTCTTTGA | 56852 |
rs166095 | snp | C/T | 0.499859 | 0.0083854 | intron-variant | RAD18 | GRCh38.p7 | 3:8887227 | gtagtctaacaagtc[C/T]tccaggtgattttaa | 56852 |
rs168186 | snp | C/T | 0.456803 | 0.140473 | intron-variant | RAD18 | GRCh38.p7 | 3:8908585 | agaaccctgctgaca[C/T]cttgatcttggactt | 56852 |
rs171029 | snp | A/G | 0.498794 | 0.0245311 | intron-variant | RAD18 | GRCh38.p7 | 3:8940797 | TATAGAACAGGGGCC[A/G]GCAAACATTCTTAGT | 56852 |
rs180498 | snp | A/G | 0.278664 | 0.248351 | intron-variant | RAD18 | GRCh38.p7 | 3:8907308 | GTTTTAGGTAGGAGA[A/G]TAAATGAAGTTATTC | 56852 |
rs193920 | snp | C/T | 0.411578 | 0.190768 | utr-variant-3-prime | RAD18 | GRCh38.p7 | 3:8878821 | ATTCTGAGCTGATGT[C/T]GATGGGAGATGTTAT | 56852 |
rs193921 | snp | A/T | 0.279726 | 0.248226 | intron-variant | RAD18 | GRCh38.p7 | 3:8889354 | aaacagggataatag[A/T]acatcatagtgttat | 56852 |
rs193922 | snp | C/T | 0.491368 | 0.0651254 | intron-variant | RAD18 | GRCh38.p7 | 3:8900150 | ATTCCTAAAAATATG[C/T]TCCTAATGTCATCTG | 56852 |
rs250400 | snp | C/T | 0.329084 | 0.237162 | downstream-variant-500B | RAD18 | GRCh38.p7 | 3:8877115 | TTTTGTATTTTGGAA[C/T]CAAAGGAGTCAGAAG | 56852 |
rs250401 | snp | A/C | 0.499609 | 0.0139722 | downstream-variant-500B | RAD18 | GRCh38.p7 | 3:8877195 | ccacagtctgggtaa[A/C]ttatagacaatagaa | 56852 |
rs250402 | snp | C/T | 0 | 0 | utr-variant-3-prime | RAD18 | GRCh38.p7 | 3:8878523 | TGAAATCCATTGTTT[C/T]TGGGTTTTTTTCCAG | 56852 |
rs250403 | snp | A/G | 0.334642 | 0.235236 | utr-variant-3-prime | RAD18 | GRCh38.p7 | 3:8878597 | ATCAGTCTTTACCAT[A/G]TAATTTTGTTTTTAA | 56852 |
rs250404 | snp | C/T | 0.499759 | 0.0109798 | utr-variant-3-prime | RAD18 | GRCh38.p7 | 3:8880370 | GCTGATGTGTTTGGG[C/T]TGGGTGATGGCAGAG | 56852 |
rs250405 | snp | C/T | 0.467132 | 0.12391 | intron-variant | RAD18 | GRCh38.p7 | 3:8883357 | ctccaggatttgttg[C/T]tgttgctgtttgcta | 56852 |
rs250406 | snp | C/T | 0.394721 | 0.203852 | intron-variant | RAD18 | GRCh38.p7 | 3:8888171 | tcctgaccacgctag[C/T]gtctttcccttgtgg | 56852 |
rs250407 | snp | A/G | 0.279726 | 0.248226 | intron-variant | RAD18 | GRCh38.p7 | 3:8889363 | taatagaacatcata[A/G]tgttatatttaaatg | 56852 |
rs250408 | snp | C/G | 0.297636 | 0.24542 | intron-variant | RAD18 | GRCh38.p7 | 3:8889754 | ATTTAGGACCTTTTA[C/G]GCATATTAAAGAGTC | 56852 |
rs250409 | snp | C/T | 0.490287 | 0.0690083 | intron-variant | RAD18 | GRCh38.p7 | 3:8889924 | ttactgtaccttttc[C/T]aggtttagatacact | 56852 |
rs250411 | snp | C/G | 0.491263 | 0.0655142 | intron-variant | RAD18 | GRCh38.p7 | 3:8900753 | GATGCTATACAAAAT[C/G]CATCTTTTCAGTCAG | 56852 |
rs341769 | snp | C/T | 0.374 | 0.217081 | intron-variant | RAD18 | GRCh38.p7 | 3:8939214 | ATATTCAGAGTCTAA[C/T]CTTGCTTTCTTTGGC | 56852 |
rs341770 | snp | G/T | 0.393987 | 0.204372 | intron-variant | RAD18 | GRCh38.p7 | 3:8938095 | TAAAGAGAAAAGCAG[G/T]TCATCAAACTCTCGT | 56852 |
rs341771 | snp | C/T | 0.405776 | 0.195535 | intron-variant | RAD18 | GRCh38.p7 | 3:8937923 | GGACGAGTATGTCTT[C/T]AAACAAACTGACAGC | 56852 |
rs341772 | snp | C/T | 0.305186 | 0.243833 | intron-variant | RAD18 | GRCh38.p7 | 3:8937608 | TCTATGACCTGACTC[C/T]GTGGCCAAGATACAA | 56852 |
rs341773 | snp | A/C | 0.462472 | 0.13174 | intron-variant | RAD18 | GRCh38.p7 | 3:8911548 | AGAGTAGGAAAAGGA[A/C]CCTAGAGGAGTCTTG | 56852 |
rs341774 | snp | A/G | 0.45645 | 0.140991 | intron-variant | RAD18 | GRCh38.p7 | 3:8910930 | TGTTACCTCTAGGGA[A/G]TGGGAATAGAGGCAG | 56852 |
rs341775 | snp | G/T | 0.45574 | 0.142025 | intron-variant | RAD18 | GRCh38.p7 | 3:8910395 | cacgaggtcaggaga[G/T]cgagaccatcctggc | 56852 |
rs341776 | snp | A/G | 0.45574 | 0.142025 | intron-variant | RAD18 | GRCh38.p7 | 3:8910323 | aagaaaaacaaggcc[A/G]ggtgcagtggctcac | 56852 |
rs341777 | snp | G/T | 0.45692 | 0.1403 | intron-variant | RAD18 | GRCh38.p7 | 3:8910093 | ccagaagagcagcca[G/T]gtattaacagaaggc | 56852 |
rs341778 | snp | A/G | 0.499087 | 0.0213463 | intron-variant | RAD18 | GRCh38.p7 | 3:8909838 | ctaacaatagctgat[A/G]agagaaaaaaaatta | 56852 |
rs341779 | snp | A/G | 0.301932 | 0.244547 | intron-variant | RAD18 | GRCh38.p7 | 3:8909495 | GACTGACAGAACTTG[A/G]TGGTGAACTGAACAT | 56852 |
rs341780 | snp | C/T | 0.45843 | 0.138046 | intron-variant | RAD18 | GRCh38.p7 | 3:8908945 | aatGGAATAGTACTA[C/T]GAAAAAACACAAGAT | 56852 |
rs341781 | snp | C/T | 0.49975 | 0.0111793 | intron-variant | RAD18 | GRCh38.p7 | 3:8908119 | ctgccacctctctct[C/T]tcctttgggttaaag | 56852 |
rs341782 | snp | A/G | 0.440471 | 0.161928 | intron-variant | RAD18 | GRCh38.p7 | 3:8907659 | AGCATCAGAGACTAC[A/G]GACAGATGCAGCTAA | 56852 |
rs341783 | snp | A/G | 0.299916 | 0.244966 | intron-variant | RAD18 | GRCh38.p7 | 3:8907067 | tctccttccagtact[A/G]tgtcctgcaaactct | 56852 |
rs341793 | snp | A/G | 0.499831 | 0.00918375 | intron-variant | RAD18 | GRCh38.p7 | 3:8957253 | tgaatctagagatca[A/G]tttgggagaattgac | 56852 |
rs367621 | snp | C/T | 0.477515 | 0.103619 | intron-variant | RAD18 | GRCh38.p7 | 3:8933472 | catgtgagtaagtta[C/T]acatcaataaaaaGG | 56852 |
rs369032 | snp | A/G | 0.475348 | 0.108251 | intron-variant | RAD18 | GRCh38.p7 | 3:8897519 | CCCCACCCTGAGAAC[A/G]CCCAGTTGGACCAGA | 56852 |
rs370342 | snp | A/G | 0.499631 | 0.0135733 | intron-variant | RAD18 | GRCh38.p7 | 3:8898035 | CGAAATCGCACCACC[A/G]CACTCCAGGCTGGGC | 56852 |
rs372806 | snp | A/G | 0.440746 | 0.161604 | intron-variant | RAD18 | GRCh38.p7 | 3:8912788 | TTTTCTATACATACT[A/G]CTTTTCTATAATGAC | 56852 |
rs373090 | snp | G/T | 0.49121 | 0.0657086 | intron-variant | RAD18 | GRCh38.p7 | 3:8900922 | TGATATTCAAGAGAG[G/T]TTCAACTAATTAAAA | 56852 |
rs373572 | snp | A/G | 0.423881 | 0.179626 | missense | RAD18 | GRCh38.p7 | 3:8913705 | CTGCTGAAATAGTTC[A/G]AGAAATCGAAAATAT | 56852 |
rs374679 | snp | A/G | 0.466412 | 0.125164 | intron-variant | RAD18 | GRCh38.p7 | 3:8933854 | agttcttccagtttt[A/G]tttattgaggttgac | 56852 |
rs375053 | snp | A/G | 0.45235 | 0.146814 | intron-variant | RAD18 | GRCh38.p7 | 3:8933709 | tcatgaatatggttt[A/G]tccccttttttgtct | 56852 |
rs375649 | snp | C/T | 0.467132 | 0.12391 | intron-variant | RAD18 | GRCh38.p7 | 3:8935095 | tgagatcactaccag[C/T]gtcccaaaagcccta | 56852 |
rs376167 | snp | G/T | 0.477515 | 0.103619 | intron-variant | RAD18 | GRCh38.p7 | 3:8885680 | gggaaaagggattta[G/T]ggtgaatgtgtggac | 56852 |
rs377012 | snp | A/C | 0.499908 | 0.00678851 | intron-variant | RAD18 | GRCh38.p7 | 3:8931587 | TCAGTGTTTTCTGAA[A/C]ACTGAGTGTAGAAAT | 56852 |
rs381604 | snp | A/G | 0.301681 | 0.2446 | intron-variant | RAD18 | GRCh38.p7 | 3:8942137 | GGGAATCACATTTCA[A/G]TGTGAGATTTGGTGG | 56852 |
rs383639 | snp | C/T | 0.461703 | 0.132974 | intron-variant | RAD18 | GRCh38.p7 | 3:8914018 | AATTTTCATATTTCA[C/T]TGAGACTTCTGTTTA | 56852 |
rs384972 | snp | C/T | 0.446249 | 0.154875 | intron-variant | RAD18 | GRCh38.p7 | 3:8933240 | atttgtgtaattcca[C/T]ttatgtgacagtcta | 56852 |
rs385253 | snp | G/T | 0.499527 | 0.0153681 | intron-variant | RAD18 | GRCh38.p7 | 3:8942780 | ATTTCTAAGCAGACT[G/T]GTGGGGTTCCCTTTC | 56852 |
rs386831 | snp | A/G | 0.452842 | 0.146134 | intron-variant | RAD18 | GRCh38.p7 | 3:8935479 | ATTATGAAGTGGGTA[A/G]TTATTATAACCCTTA | 56852 |
rs395559 | snp | A/G | 0.456214 | 0.141336 | intron-variant | RAD18 | GRCh38.p7 | 3:8917188 | gaattctggattggc[A/G]ggcttttttctaatg | 56852 |
rs398518 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | RAD18 | GRCh38.p7 | 3:8913275 | TCTGGCATTCTGCAA[C/T]TCTATGATTATACTT | 56852 |
rs406333 | snp | C/T | 0.452597 | 0.146474 | intron-variant | RAD18 | GRCh38.p7 | 3:8934335 | ATGTATGTACATTTC[C/T]AATTTCACcttttca | 56852 |
rs407176 | snp | A/T | 0.494187 | 0.0535994 | intron-variant | RAD18 | GRCh38.p7 | 3:8916703 | tactgtgttggtttt[A/T]tgtgtctatatctat | 56852 |
rs408483 | snp | C/T | 0.451732 | 0.147663 | intron-variant | RAD18 | GRCh38.p7 | 3:8933516 | tatagtttccttata[C/T]ccAATGGCTTGTCGC | 56852 |
rs409144 | snp | A/C | 0.266819 | 0.249434 | intron-variant | RAD18 | GRCh38.p7 | 3:8941976 | ATTAACTGCCTTTTA[A/C]GTTAGATTTATTGCT | 56852 |
rs413925 | snp | A/T | 0.387832 | 0.208572 | intron-variant | RAD18 | GRCh38.p7 | 3:8905168 | ATGTGTCCTGGATTT[A/T]CCTCTTAAAAGTTTT | 56852 |
rs415015 | snp | A/T | 0.499104 | 0.0211472 | intron-variant | RAD18 | GRCh38.p7 | 3:8916043 | AGGGATAAAGATGTG[A/T]TTGGGGCTTCATGTC | 56852 |
rs421320 | snp | A/C | 0 | 0 | intron-variant | RAD18 | GRCh38.p7 | 3:8882473 | gaggaggtggaagtg[A/C]tgagaaaggcccacc | 56852 |
rs424289 | snp | A/C | | | intron-variant | RAD18 | GRCh38.p7 | 3:8953235 | tacttatataggtac[A/C]attacatatataata | 56852 |
rs427428 | snp | C/T | 0.266819 | 0.249434 | intron-variant | RAD18 | GRCh38.p7 | 3:8902095 | CCAATAAATTCTATA[C/T]CTAGAAAACATCCTG | 56852 |
rs428961 | snp | A/G | 0.488485 | 0.0749998 | intron-variant | RAD18 | GRCh38.p7 | 3:8935475 | CAACATTATGAAGTG[A/G]GTAGTTATTATAACC | 56852 |
rs430781 | snp | A/G | 0.275197 | 0.248727 | intron-variant | RAD18 | GRCh38.p7 | 3:8913556 | GCCATTATTAAATTT[A/G]TTCATTTACTAACAC | 56852 |
rs435936 | snp | C/T | 0.452842 | 0.146134 | intron-variant | RAD18 | GRCh38.p7 | 3:8934431 | gtttaaatctatgtc[C/T]aattcttctgttctg | 56852 |
rs439848 | snp | A/T | 0.499631 | 0.0135733 | intron-variant | RAD18 | GRCh38.p7 | 3:8898094 | TGAAAAAAAAAGTAT[A/T]CAATAGAAACAAAGG | 56852 |
rs440496 | snp | C/G | 0.278399 | 0.248382 | intron-variant | RAD18 | GRCh38.p7 | 3:8931599 | CATTCTTGTTGTTCA[C/G]TGTTTTCTGAAAACT | 56852 |
rs445056 | snp | A/T | 0.462253 | 0.132093 | intron-variant | RAD18 | GRCh38.p7 | 3:8931858 | cattgtcaaatccta[A/T]cggccatgtatatag | 56852 |
rs446270 | snp | C/T | 0.452103 | 0.147154 | intron-variant | RAD18 | GRCh38.p7 | 3:8933196 | gcattttacatatgg[C/T]atctgtcacttagca | 56852 |
rs446596 | snp | C/G | 0.498734 | 0.0251279 | intron-variant | RAD18 | GRCh38.p7 | 3:8936297 | GAAGTGAGAGACTTG[C/G]GTCTCAAAAAGAGGT | 56852 |
rs446923 | snp | C/G | 0.450985 | 0.148678 | intron-variant | RAD18 | GRCh38.p7 | 3:8933552 | accagttgtattttt[C/G]tgtacaagcaactaa | 56852 |
rs447423 | snp | C/T | 0.468349 | 0.121752 | intron-variant | RAD18 | GRCh38.p7 | 3:8934058 | tgatgcagcaccact[C/T]attgaaatgccatcc | 56852 |
rs462153 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RAD18 | GRCh38.p7 | 3:8902288 | TTCAAAGAACTAAGA[A/G]CTCCAAAGTAAATTT | 56852 |
rs464302 | snp | A/C | 0.499663 | 0.0129749 | intron-variant | RAD18 | GRCh38.p7 | 3:8902304 | CTCCAAAGTAAATTT[A/C]TTTGGTTTAATTTTT | 56852 |
rs473836 | snp | C/T | 0.499977 | 0.00339449 | intron-variant | RAD18 | GRCh38.p7 | 3:8928254 | ttcatttcctgcttt[C/T]ttttggattaactga | 56852 |
rs474008 | snp | A/T | 0.475702 | 0.107512 | intron-variant | RAD18 | GRCh38.p7 | 3:8921640 | GTCTTGttttttttt[A/T]aagatagggtcttgc | 56852 |
rs477548 | snp | A/G | 0.443866 | 0.157848 | intron-variant | RAD18 | GRCh38.p7 | 3:8927852 | tgttgtcattgttca[A/G]ttcccacctatgagt | 56852 |
rs481748 | snp | A/G | 0.279195 | 0.248289 | intron-variant | RAD18 | GRCh38.p7 | 3:8901992 | CTACCAGGTATGTTA[A/G]CTTTAGACTGTTTGG | 56852 |
rs481976 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | RAD18 | GRCh38.p7 | 3:8901911 | CCAAAGCCCAGGCAA[C/T]AGAATTAAAATATCA | 56852 |
rs484453 | snp | A/T | 0.462516 | 0.13167 | intron-variant | RAD18 | GRCh38.p7 | 3:8908273 | aaagaaaaaaaaaaa[A/T]gcttaaagtgaatag | 56852 |
rs491254 | snp | C/G | 0.461592 | 0.133149 | intron-variant | RAD18 | GRCh38.p7 | 3:8923533 | gaatgtgaatgttgg[C/G]ctgccttgctagact | 56852 |
rs499147 | snp | C/T | 0.464841 | 0.127841 | intron-variant | RAD18 | GRCh38.p7 | 3:8930679 | gacaattcaacacgc[C/T]ttcataataataaac | 56852 |
rs500064 | snp | A/T | 0.299916 | 0.244966 | intron-variant | RAD18 | GRCh38.p7 | 3:8930591 | tttataacattgAGt[A/T]ttaatcagtttattg | 56852 |
rs500938 | snp | G/T | 0.460365 | 0.13508 | intron-variant | RAD18 | GRCh38.p7 | 3:8921040 | TTTACCCTTTACCCC[G/T]AAATatgTCCTTGTA | 56852 |
rs516491 | snp | A/G | 0.300169 | 0.244914 | intron-variant | RAD18 | GRCh38.p7 | 3:8946713 | GCTATATATTAATCT[A/G]TTAATTCTTAATCGG | 56852 |
rs518319 | snp | A/T | 0.494057 | 0.0541878 | intron-variant | RAD18 | GRCh38.p7 | 3:8946516 | CTTTTAGTTTTAATC[A/T]TGCAAGTCAAGCAAG | 56852 |
rs519999 | snp | A/G | 0.499913 | 0.00658888 | intron-variant | RAD18 | GRCh38.p7 | 3:8946364 | gtgtgaacatcatac[A/G]gtgtacttacacaaa | 56852 |
rs523858 | snp | C/T | 0.465263 | 0.127129 | intron-variant | RAD18 | GRCh38.p7 | 3:8930247 | tgtggtcaatactca[C/T]ttatttttcattgcc | 56852 |
rs524665 | snp | A/G | 0.450231 | 0.149691 | intron-variant | RAD18 | GRCh38.p7 | 3:8930185 | tctttgtgtctgttc[A/G]ttagttcaaatctga | 56852 |
rs524898 | snp | C/T | 0.465473 | 0.126772 | intron-variant | RAD18 | GRCh38.p7 | 3:8930103 | tacaaatttttatgt[C/T]gacatatgttttcat | 56852 |
rs525708 | snp | A/C | 0.465473 | 0.126772 | intron-variant | RAD18 | GRCh38.p7 | 3:8930049 | gtagaattgctgagt[A/C]gtatggtaattctat | 56852 |
rs526605 | snp | A/G | 0.465473 | 0.126772 | intron-variant | RAD18 | GRCh38.p7 | 3:8929966 | tacatcctactagca[A/G]tgtataagagttcca | 56852 |
rs527649 | snp | A/G | 0.465473 | 0.126772 | intron-variant | RAD18 | GRCh38.p7 | 3:8929831 | acagggtgaaacccc[A/G]tctctacttaaaata | 56852 |
rs528203 | snp | C/G | 0.463666 | 0.129795 | intron-variant | RAD18 | GRCh38.p7 | 3:8920379 | tcaactttagcattg[C/G]tttcacagttgctaa | 56852 |
rs529369 | snp | A/G | 0.461923 | 0.132621 | intron-variant | RAD18 | GRCh38.p7 | 3:8929664 | acagagtgagactcc[A/G]tctcaaaaaaaaaaa | 56852 |
rs531787 | snp | C/G | 0.299664 | 0.245017 | intron-variant | RAD18 | GRCh38.p7 | 3:8943576 | ttctttctgttcctt[C/G]tgggcttttaattat | 56852 |
rs540004 | snp | C/T | 0.461703 | 0.132974 | intron-variant | RAD18 | GRCh38.p7 | 3:8925690 | aagctttttgatgtg[C/T]tgctggattcggttt | 56852 |
rs546164 | snp | C/G | 0.452103 | 0.147154 | intron-variant | RAD18 | GRCh38.p7 | 3:8932960 | tacaggtgcctgcca[C/G]cacgcccggctaatt | 56852 |