SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs714181 | snp | C/T | 0.233149 | 0.249431 | missense | SLX4 | GRCh38.p7 | 16:3590273 | TCCCAGAAAAATCTC[C/T]GTCTATTGACCTAAC | 84464 |
rs758748 | snp | A/G | 0.129664 | 0.219133 | intron-variant | SLX4 | GRCh38.p7 | 16:3583656 | ACTTCTGTGAGCATC[A/G]GAGGTTAGTGTCTAT | 84464 |
rs1056084 | snp | A/C/T | 0.000124293 | 0.00788233 | synonymous-codon | SLX4 | GRCh38.p7 | 16:3596232 | GGCCCTGCAGGACCT[A/C/T]GTGGACCTGGCGAGG | 84464 |
rs1056085 | snp | A/G/T | 0.00958616 | 0.0685978 | missense | SLX4 | GRCh38.p7 | 16:3596179 | GGCCCGGCAGTGGGG[A/G/T]CCTGGCTGGCTCGGA | 84464 |
rs1061002 | snp | A/G | 0 | 0 | missense | SLX4 | GRCh38.p7 | 16:3592798 | GCGGCCTCGGTGCTC[A/G]CGTCACCCAGCAGGA | 84464 |
rs1962216 | snp | C/T | | | intron-variant | SLX4 | GRCh38.p7 | 16:3605929 | gatggagtctcgctc[C/T]gtcacccaggctgga | 84464 |
rs1962217 | snp | A/G | | | intron-variant | SLX4 | GRCh38.p7 | 16:3605920 | tcgctccgtcaccca[A/G]gctggagtgcagtgg | 84464 |
rs1989387 | snp | A/G | 0.499908 | 0.00678851 | intron-variant | SLX4 | GRCh38.p7 | 16:3604598 | GAGACTGAGGTGGAC[A/G]GATCACAAGGTCAGG | 84464 |
rs2010056 | snp | A/G | 0 | 0 | intron-variant | SLX4 | GRCh38.p7 | 16:3587257 | atcccagcactttgg[A/G]aggccgaggtgggcg | 84464 |
rs2240883 | snp | C/G | 0.126909 | 0.217598 | intron-variant | SLX4 | GRCh38.p7 | 16:3595908 | CAGACAGTTCACCCA[C/G]AGGATTCACTCGCTG | 84464 |
rs2240884 | snp | C/G | 0.000495254 | 0.0157284 | intron-variant | SLX4 | GRCh38.p7 | 16:3596109 | GCGGGGAGGGGAGGC[C/G]CGGGAGGGCAGGGCT | 84464 |
rs2240885 | snp | A/G | 0.480853 | 0.0959518 | intron-variant | SLX4 | GRCh38.p7 | 16:3597097 | AAGTGCAGGGATTAC[A/G]GGCGTGAGCCACTGC | 84464 |
rs3214313 | in-del | -/C | 0.00438332 | 0.0466095 | intron-variant | SLX4 | GRCh38.p7 | 16:3592611 | TTCTCTTGGCCTCAG[-/C]CCCGAGCCCTCTGCA | 84464 |
rs3751839 | snp | C/T | 0.134531 | 0.221736 | utr-variant-3-prime | SLX4 | GRCh38.p7 | 16:3582334 | GGGGTGGGGTCGGGA[C/T]GGCCCCATCAGTTCC | 84464 |
rs3751840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense | SLX4 | GRCh38.p7 | 16:3598517 | TTATACCAGCCGCCC[C/T]GGGACTCTGCACTTT | 84464 |
rs3810812 | snp | A/G | 0.475097 | 0.108772 | synonymous-codon | SLX4 | GRCh38.p7 | 16:3589138 | AAAGCTCGGCCTGCT[A/G]TTCCCCAGGGAGCCC | 84464 |
rs3810813 | snp | A/G | 0.120094 | 0.213599 | missense | SLX4 | GRCh38.p7 | 16:3589826 | CTGATTTGGGTCTGG[A/G]AAGAACAGTCACGGC | 84464 |
rs3810814 | snp | C/T | 0.000732308 | 0.0191211 | synonymous-codon | SLX4 | GRCh38.p7 | 16:3589876 | GGCGGGCACCAGCCA[C/T]GAGGTGTCTGTGGTG | 84464 |
rs3827530 | snp | A/G | 0.110302 | 0.207327 | missense | SLX4 | GRCh38.p7 | 16:3589976 | CGATTCTCCGGCAGC[A/G]CCCCCTCATCCTCCT | 84464 |
rs3833838 | in-del | -/G | | | utr-variant-3-prime | SLX4 | GRCh38.p7 | 16:3582302 | ATGGCGGGGGTGGGG[-/G]CTGCTGATGGCAGGT | 84464 |
rs7196345 | snp | A/G | 0.00297714 | 0.0384669 | missense | SLX4 | GRCh38.p7 | 16:3583221 | GCGACCTGCTTGGGG[A/G]TGTGATGCTTTCATG | 84464 |
rs7198338 | snp | A/G | 0.00613123 | 0.0550275 | synonymous-codon, upstream-variant-2KB | SLX4 | GRCh38.p7 | 16:3601143 | AATCGGGCACTCAGG[A/G]ATCTGAGGCACAGAA | 84464 |
rs7199766 | snp | A/G | 0.35207 | 0.228214 | intron-variant | SLX4 | GRCh38.p7 | 16:3587428 | ttgaacccgagaggt[A/G]gaggttgcagtgagc | 84464 |
rs8058233 | snp | A/G | 0.499087 | 0.0213463 | intron-variant | SLX4 | GRCh38.p7 | 16:3588808 | ACTGACTTACTGGCT[A/G]AGAAGTGTAGCATGA | 84464 |
rs8061528 | snp | C/T | 0.336193 | 0.23468 | synonymous-codon | SLX4 | GRCh38.p7 | 16:3606481 | CATCATACCATTCCC[C/T]GCCATCATCTCCTCT | 84464 |
rs9923287 | snp | C/T | 0.186737 | 0.241863 | intron-variant | SLX4 | GRCh38.p7 | 16:3583855 | AAAAAATACAAAAAT[C/T]AGCCAGGCGTGGTGG | 84464 |
rs9937425 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | SLX4 | GRCh38.p7 | 16:3584236 | gaccagcctggccaa[C/T]atggtgaaaccccgt | 84464 |
rs11076781 | snp | A/G | 0.357238 | 0.225832 | upstream-variant-2KB, intron-variant | SLX4, DNASE1 | GRCh38.p7 | 16:3613230 | TAAATGGGATCATGT[A/G]ATACTTGGCTTTTTC | 84464 |
rs11646156 | snp | C/G | 0.0295035 | 0.117819 | intron-variant, missense | SLX4 | GRCh38.p7 | 16:3598545 | TTTCAACGGGCAGCA[C/G]CTCGTTTGGTTTGGA | 84464 |
rs11866834 | snp | C/G | | | intron-variant | SLX4 | GRCh38.p7 | 16:3585564 | gcactccagcctggg[C/G]gacagagcaagactc | 84464 |
rs12148934 | snp | C/G | 0.0236746 | 0.106192 | intron-variant, utr-variant-5-prime | SLX4 | GRCh38.p7 | 16:3598733 | AGCTCATGCTCTCCA[C/G]GGTGCCAGGGATGGC | 84464 |
rs12149539 | snp | C/T | 0 | 0 | intron-variant | SLX4 | GRCh38.p7 | 16:3600509 | CCTCCTCACTCCCTT[C/T]TAGACTGTGCCCGAT | 84464 |
rs12448212 | snp | C/G | 0.130694 | 0.219696 | intron-variant | SLX4 | GRCh38.p7 | 16:3586808 | gggcaacagagagag[C/G]ctccgtctcaaaaaa | 84464 |
rs12598304 | snp | A/T | | | intron-variant | SLX4 | GRCh38.p7 | 16:3593391 | taggctaatttttaa[A/T]tttttttgtagagat | 84464 |
rs12924990 | snp | C/T | 0.143284 | 0.226079 | upstream-variant-2KB, utr-variant-5-prime, intron-variant, nc-transcript-variant | SLX4, DNASE1 | GRCh38.p7 | 16:3611814 | TTTTTGAGAAAGAGT[C/T]AGGGCGAGTTTAAGG | 84464 |
rs12933120 | snp | A/C | 0.182434 | 0.240697 | intron-variant | SLX4 | GRCh38.p7 | 16:3584745 | AAAGACCACTGTGGG[A/C]AACAAGCTTTGAAGA | 84464 |
rs13335275 | snp | A/G | 0.237593 | 0.249692 | intron-variant | SLX4 | GRCh38.p7 | 16:3585309 | ATGGGCAAAGGGGCC[A/G]GGCGCGGTGGCTCAC | 84464 |
rs13335490 | snp | C/T | 0.105569 | 0.204058 | intron-variant | SLX4 | GRCh38.p7 | 16:3600428 | TTGAGGAAAACAGTG[C/T]GAAGATCATTTCTGC | 84464 |
rs17136464 | snp | C/T | 0.000265927 | 0.0115279 | missense | SLX4 | GRCh38.p7 | 16:3589539 | GCCTGCTGAAGTGGG[C/T]GCGGTCCCCTGAGAT | 84464 |
rs28516461 | snp | A/G | 0.103174 | 0.202342 | synonymous-codon | SLX4 | GRCh38.p7 | 16:3606556 | GCACTCTTCTGAAGC[A/G]TGTCTCAAACGCTCG | 84464 |
rs28612736 | snp | G/T | 0 | 0 | missense | SLX4 | GRCh38.p7 | 16:3608776 | CTTGATTCCATGTTT[G/T]TTCACCCTTTGGAAA | 84464 |
rs28840400 | snp | A/G | 0.153 | 0.230415 | intron-variant | SLX4 | GRCh38.p7 | 16:3605033 | TCAAGCAATCCTCCC[A/G]CCTCAGCCTCCCGAG | 84464 |
rs34644639 | in-del | -/G | | | frameshift-variant | SLX4 | GRCh38.p7 | 16:3592711 | ACCTGTGGGCCAGGG[-/G]AGCTCAGCTCAGAGC | 84464 |
rs34760860 | in-del | -/C | | | intron-variant | SLX4 | GRCh38.p7 | 16:3586444 | GAGGATCACTTGAGC[-/C]TGGGAGGTCGAGGCT | 84464 |
rs34903148 | in-del | -/C | | | frameshift-variant | SLX4 | GRCh38.p7 | 16:3590665 | TCTGAGATCTCTCCC[-/C]TGAGTTGATGAGAAG | 84464 |
rs34915806 | in-del | -/G | | | upstream-variant-2KB, intron-variant | SLX4, DNASE1 | GRCh38.p7 | 16:3612600 | GGGGGCGGGGGGGGG[-/G]AGTCTCACTATGTTG | 84464 |
rs34956662 | snp | A/C | 0.277778 | 0.248452 | intron-variant | SLX4 | GRCh38.p7 | 16:3584374 | TGCAGTGAGCCGGGA[A/C]TGCGCCACTGCACTC | 84464 |
rs35085629 | in-del | -/T | | | upstream-variant-2KB, intron-variant | SLX4, DNASE1 | GRCh38.p7 | 16:3612568 | TTTTTTTTTTTTTTT[-/T]AAGTAGAGACGGGCG | 84464 |
rs35181087 | in-del | -/A | 0.478685 | 0.10101 | intron-variant | SLX4 | GRCh38.p7 | 16:3585603 | GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 84464 |
rs35191705 | in-del | -/G | | | downstream-variant-500B, intron-variant, nc-transcript-variant | SLX4, LOC105371060 | GRCh38.p7 | 16:3580764 | CCTTCAAGCCACTGG[-/G]AGCCCGACTCCCCAC | 84464 |
rs35214951 | in-del | -/A | 0.37778 | 0.214877 | intron-variant | SLX4 | GRCh38.p7 | 16:3604819 | AAAAAAAAAAAAAAA[-/A]TGTATATTTATAAAG | 84464 |
rs35374307 | in-del | -/G | | | intron-variant | SLX4 | GRCh38.p7 | 16:3583862 | CAAAAATTAGCCAGG[-/G]CGTGGTGGTGTCACC | 84464 |
rs35453634 | in-del | -/C | | | intron-variant | SLX4 | GRCh38.p7 | 16:3593848 | AAAGAGAAAACAATT[-/C]CTGGGAAACAATGGA | 84464 |
rs35564933 | in-del | -/A | | | intron-variant | SLX4 | GRCh38.p7 | 16:3604166 | AACCTGGGAGGCAGA[-/A]GGTTGCAGTGAACCG | 84464 |
rs35570194 | in-del | -/G | | | frameshift-variant | SLX4 | GRCh38.p7 | 16:3597880 | CCATCTCCGACCGGG[-/G]ACAGAGCCATGGCCA | 84464 |
rs35603561 | in-del | -/G | | | frameshift-variant | SLX4 | GRCh38.p7 | 16:3589312 | GCCGGTCCGCTCCAG[-/G]TTCCAGTGGTCAATG | 84464 |
rs35722907 | in-del | -/G | | | intron-variant | SLX4 | GRCh38.p7 | 16:3587029 | GGCTGGGGGAAGGGG[-/G]AAGGTGAGAGACTGC | 84464 |
rs35996000 | in-del | -/G | | | intron-variant | SLX4 | GRCh38.p7 | 16:3587270 | GGAAGGCCGAGGTGG[-/G]CGGATCACCTGAGGT | 84464 |
rs36003440 | in-del | -/G | | | frameshift-variant | SLX4 | GRCh38.p7 | 16:3583395 | CGCCTGCAACAGCGG[-/G]CTGTGAGGACTGGCT | 84464 |
rs36033450 | in-del | -/G | | | intron-variant, frameshift-variant | SLX4 | GRCh38.p7 | 16:3598485 | GGCTTCCCAGCTTAG[-/G]CTGCCGATGGTCAAC | 84464 |
rs55645258 | snp | A/C | 0.103438 | 0.202533 | intron-variant | SLX4 | GRCh38.p7 | 16:3603478 | GGTGCCTCCTCTGCA[A/C]CTCACATGTGCGTCC | 84464 |
rs55768314 | snp | G/T | 0.111576 | 0.20818 | intron-variant | SLX4 | GRCh38.p7 | 16:3607252 | GATTTCATCCGACTG[G/T]CAAAGAGCACGAGAG | 84464 |
rs55785211 | in-del | -/T | | | intron-variant | SLX4 | GRCh38.p7 | 16:3596839 | TTTTTTTTTTTTTTT[-/T]CAAGACAGAGTCTCA | 84464 |
rs55868835 | snp | A/G | 0.103082 | 0.202275 | intron-variant | SLX4 | GRCh38.p7 | 16:3596854 | TCAAGACAGAGTCTC[A/G]CTTTGTTGCCCAGGC | 84464 |
rs55964569 | snp | A/C/G | 0.0189856 | 0.0955633 | intron-variant | SLX4 | GRCh38.p7 | 16:3603508 | CAGGACTGATGCCTC[A/C/G]GCAGGACATCAAATC | 84464 |
rs56211607 | snp | A/T | 0.140242 | 0.224618 | intron-variant | SLX4 | GRCh38.p7 | 16:3593528 | TGGTCCCTAGTCTTA[A/T]AAGCAGCTCCATGCC | 84464 |
rs56242256 | in-del | -/A | | | intron-variant, frameshift-variant | SLX4 | GRCh38.p7 | 16:3598565 | TTTGGTTTGGAGGAA[-/A]TGAACAGGAGTTTCC | 84464 |
rs56747562 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | SLX4 | GRCh38.p7 | 16:3605306 | GTGTTAGCCAGGATG[G/T]TCTCAATCTCCTGAC | 84464 |
rs57664740 | in-del | -/G | 0.0158469 | 0.0875917 | intron-variant | SLX4 | GRCh38.p7 | 16:3608100 | TGAGGCACGAGGATT[-/G]CTTGAGTCCAGGAGT | 84464 |
rs57699393 | snp | A/G | 0.0356815 | 0.128715 | utr-variant-3-prime, downstream-variant-500B | SLX4, LOC105371060 | GRCh38.p7 | 16:3581358 | CAAAGAATGGAATCC[A/G]CTAGTGAACATGTTT | 84464 |
rs57747758 | snp | C/T | 0.112631 | 0.208878 | intron-variant | SLX4 | GRCh38.p7 | 16:3605175 | GCTCACTGCAAGCTC[C/T]GTCTCCCAGGTTCAC | 84464 |
rs57910835 | snp | C/G | 0.153 | 0.230415 | utr-variant-5-prime | SLX4 | GRCh38.p7 | 16:3609323 | AGAGGCAAGAGAATC[C/G]CTTGAACCTGGGAGG | 84464 |
rs58360168 | snp | C/G | 0.103082 | 0.202275 | intron-variant | SLX4 | GRCh38.p7 | 16:3593950 | AATCTCAGCTCATTG[C/G]AAGCTCCGCCTCCCA | 84464 |
rs58380344 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | SLX4, DNASE1 | GRCh38.p7 | 16:3612014 | CCTCTCAGGTGGGGT[A/G]GCGTGAGAGTCGAGG | 84464 |
rs58407102 | snp | A/G | 0.103082 | 0.202275 | intron-variant | SLX4 | GRCh38.p7 | 16:3594119 | TGATCTGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 84464 |
rs58638942 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | SLX4 | GRCh38.p7 | 16:3603793 | CACTGTCGCCACCCT[A/G]TCTCACCTGCAGCCA | 84464 |
rs58735123 | snp | A/G | 0.00586631 | 0.05384 | synonymous-codon | SLX4 | GRCh38.p7 | 16:3590529 | CCTGGGGAGGCCCCA[A/G]TAGGAAGCGGCACGG | 84464 |
rs59127692 | snp | A/G | 0.155325 | 0.23138 | intron-variant, upstream-variant-2KB | SLX4, DNASE1 | GRCh38.p7 | 16:3609738 | CCTATCAGACATCAC[A/G]ACAAAAGGACCTAGA | 84464 |
rs59311338 | snp | C/T | 0.127599 | 0.217986 | utr-variant-5-prime | SLX4 | GRCh38.p7 | 16:3609259 | TGAAAATACAAAAAA[C/T]TGGCCAGGCGTGGTA | 84464 |
rs59325374 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant, utr-variant-5-prime | SLX4 | GRCh38.p7 | 16:3599055 | CATCTAGTTTCAGTA[C/T]TTGGAGGTATTCTAA | 84464 |
rs59622164 | snp | C/G | 0.102201 | 0.20229 | intron-variant | SLX4 | GRCh38.p7 | 16:3598074 | GGTCACACTGGTCTG[C/G]AGAGGGCTGGGCCTG | 84464 |
rs59706816 | snp | A/G | 0.00335997 | 0.0408496 | missense | SLX4 | GRCh38.p7 | 16:3596275 | TGGCTGGCCGAAGGC[A/G]ACGGGCCCCTGGAGC | 84464 |
rs59939128 | snp | C/T | 0.125448 | 0.216764 | missense | SLX4 | GRCh38.p7 | 16:3590784 | TGGAATGGCCAAGCG[C/T]CTCCTCTGGCGCCTC | 84464 |
rs60065695 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SLX4 | GRCh38.p7 | 16:3594963 | CCCATCCCCTGTGAC[A/G]GACAAGCACCCTGAG | 84464 |
rs60163083 | snp | A/G | 0.11963 | 0.213316 | intron-variant, upstream-variant-2KB | SLX4 | GRCh38.p7 | 16:3601423 | TAAATGCAGTTACAT[A/G]ATGACTTAGAAATTC | 84464 |
rs60172682 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | SLX4 | GRCh38.p7 | 16:3606323 | GACTCTTCATTCTCT[C/G]GCTGGATCCAGTGAA | 84464 |
rs60298844 | snp | C/T | 0.124144 | 0.21601 | intron-variant, missense | SLX4 | GRCh38.p7 | 16:3598618 | CTGGGTGACTCCCAA[C/T]AAGCTGGGCAAGAAG | 84464 |
rs60409031 | snp | A/T | 0.124491 | 0.216211 | intron-variant, upstream-variant-2KB | SLX4 | GRCh38.p7 | 16:3602823 | GAAATGCCTTTGGCG[A/T]TTAAAAGGCAGCATC | 84464 |
rs60876027 | snp | C/T | 0.0244538 | 0.107838 | intron-variant, upstream-variant-2KB | SLX4 | GRCh38.p7 | 16:3602992 | CTTCATGGCTGTGGC[C/T]TACCAGTGCCTGCCA | 84464 |
rs60918224 | snp | A/G | 0.126909 | 0.217598 | intron-variant, upstream-variant-2KB | SLX4, DNASE1 | GRCh38.p7 | 16:3609794 | CACAGGTATTAAAAT[A/G]TGTGCATCTTGGGAG | 84464 |
rs61031231 | snp | A/C | | | missense | SLX4 | GRCh38.p7 | 16:3582630 | CTGCGAGGCACTGAC[A/C]TCCCCCTCGCCCTCC | 84464 |
rs61188361 | snp | C/G | 0.113334 | 0.209338 | intron-variant | SLX4 | GRCh38.p7 | 16:3605359 | CTCCCAAAGTGCTGG[C/G]ATTACAGGCGTGAGC | 84464 |
rs61468947 | snp | A/G | 0.0158469 | 0.0875917 | upstream-variant-2KB, intron-variant | SLX4, DNASE1 | GRCh38.p7 | 16:3613273 | ATTAAGCATGTTTTC[A/G]AGATTTCATCCATGT | 84464 |
rs62037799 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | SLX4 | GRCh38.p7 | 16:3598149 | CACTTCCACTGCCTT[G/T]TGTGAACTCATTCAA | 84464 |
rs71133646 | in-del | -/A | | | intron-variant | SLX4 | GRCh38.p7 | 16:3586365 | GTCTCTACTAAAAAA[-/A]AAAAAATTAGCTGGG | 84464 |
rs71133647 | in-del | -/G | 0 | 0 | intron-variant | SLX4 | GRCh38.p7 | 16:3605924 | GCACTCCAGCCTGGG[-/G]TGACGGAGCGAGACT | 84464 |
rs71388524 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, downstream-variant-500B | SLX4, LOC105371060 | GRCh38.p7 | 16:3581250 | ATTTGAAACAGACGA[A/G]GACATTCACAAGGAT | 84464 |
rs71388525 | snp | A/G | 0.5 | 0 | intron-variant | SLX4 | GRCh38.p7 | 16:3600256 | AGGAGGCGGAGCTCA[A/G]GCAGTAAAGCTTGCC | 84464 |
rs71388526 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SLX4 | GRCh38.p7 | 16:3600780 | TTTGTATTTTTAGTA[A/C/G]AGACGAGATTGTACC | 84464 |
rs71388527 | snp | A/G | 0.5 | 0 | intron-variant | SLX4 | GRCh38.p7 | 16:3600787 | TTTTAGTAGAGACGA[A/G]ATTGTACCATGTCGG | 84464 |