SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs9679 | snp | A/C | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1943285 | TCATTAAAGATAAAA[A/C]ACAGCCAAAGANTCT | 7468 |
rs14647 | snp | A/C | 0.00159617 | 0.0282053 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1982108 | GCTATTTTCCCCCAA[A/C]TGGCAAGTCTCAACT | 7468 |
rs373763 | snp | A/G | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1917779 | aaaaaaaaaaaaaaa[A/G]gaaTACTTTTACATT | 7468 |
rs410630 | snp | A/T | 0.26326 | 0.249648 | intron-variant | WHSC1 | GRCh38.p7 | 4:1925774 | AAACAAACaaaaaaa[A/T]atataTATatagata | 7468 |
rs426891 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931216 | GGACCCCTGTAAGGT[A/G]CAGACTACAGCCGAA | 7468 |
rs465686 | snp | A/C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1933685 | CTTGCAGggccgggc[A/C/G]cggtggcctcacacc | 7468 |
rs474235 | snp | C/T | 0.431325 | 0.172108 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959410 | CCGAATACCCTTGCA[C/T]ACCCACCACTGCCTC | 7468 |
rs478530 | snp | A/G | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1972492 | CACTGTCACCCCCAG[A/G]ACACGCCCACCCTTC | 7468 |
rs479534 | snp | A/G | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1972346 | CTACAACGAGCTTGC[A/G]CTGGGGAAGATTTCC | 7468 |
rs487903 | snp | A/G | 0.42803 | 0.175514 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1900182 | CATAAAAGCAAAATC[A/G]ACACTAACAGGAAAA | 7468 |
rs489015 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1950574 | CCGGGGTGGAGACCA[C/T]GCGTCCTTTCAGAAG | 7468 |
rs489550 | snp | C/T | 0.00187459 | 0.0305578 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1953218 | CTTCAGAGGCAGCCA[C/T]GCTGCTAAAGCACCT | 7468 |
rs494893 | snp | C/T | 0.224116 | 0.248656 | intron-variant | WHSC1 | GRCh38.p7 | 4:1956444 | TTCTGTAAATTAGTA[C/T]TAAAAATAATTTCTG | 7468 |
rs495403 | snp | C/T | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1949883 | GACCTTATCAGTGAG[C/T]TTTTCCACATTTAGC | 7468 |
rs496909 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891791 | cggctcactgcaagc[C/T]ccgcctcccgtgttc | 7468 |
rs508436 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1956260 | ATAAAGATCAAATTT[A/T]AAAAAATAGAAATTA | 7468 |
rs514882 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1936690 | ACTACTCTGTCAGAA[C/T]TTTTTTTTTTTTTTT | 7468 |
rs515582 | snp | A/C | 0 | 0 | missense | WHSC1 | GRCh38.p7 | 4:1978745 | GGGTGCAGCTGAAGG[A/C]TGTCCCGTCCTGGTG | 7468 |
rs527355 | snp | C/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1919553 | TCTCATGCTTAAAAG[C/G]TTTTTTAGTGTTCAT | 7468 |
rs527357 | snp | C/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1919554 | CTCATGCTTAAAAGC[C/T]TTTTTAGTGTTCATT | 7468 |
rs528915 | snp | A/C | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906084 | CTGCTTGTGTGCCAC[A/C]CAAACAAATAACATG | 7468 |
rs530972 | snp | A/T | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1892915 | CCTCAGTAAAAAAAA[A/T]ACAGAGGTTAAACAA | 7468 |
rs536143 | snp | C/G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1923418 | TTCTGAAGGAGAAGG[C/G/T]GAAGTCTTTTGGAGA | 7468 |
rs544270 | snp | A/G | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906074 | GCCACCCAAACAAAT[A/G]ACATGGGAGTCACAG | 7468 |
rs546761 | snp | A/C | 0 | 0 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893726 | gaaatcttgtctctg[A/C]aaaaaaatacaaaaa | 7468 |
rs546903 | snp | C/T | | | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942136 | ATTTATCACATATAC[C/T]TTTTCAGAAGATTTA | 7468 |
rs554570 | snp | A/T | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1906122 | TAAATATCCCCAGAC[A/T]CTAAAAAGGAAATCA | 7468 |
rs568163 | snp | G/T | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1924613 | ACTGAAGGTATACAG[G/T]TAAAACTGAGTTCTG | 7468 |
rs570175 | snp | G/T | 0.143622 | 0.226238 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951444 | GTGTGTGTGTGTGTG[G/T]ATTACATGATGTGTA | 7468 |
rs573656 | snp | A/G/T | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1934847 | ttttttttttttttt[A/G/T]agatggagtctcgct | 7468 |
rs618034 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1924769 | ccgttaattttcttg[G/T]tttgttttgtttttt | 7468 |
rs632238 | snp | C/T | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923903 | GTATGTGGCCCTTTT[C/T]AAACTACACAAGTGA | 7468 |
rs644646 | snp | A/G | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923426 | TTACTGGCTCTCCAA[A/G]AAACTTGCCCTTCTC | 7468 |
rs673873 | snp | C/G | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1914906 | CCAACTAAAACAGTC[C/G]TAAGTGTCCCACTGC | 7468 |
rs673878 | snp | C/G | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1914897 | ACAGTCCTAAGTGTC[C/G]CACTGCAACATCCAC | 7468 |
rs673887 | snp | A/G | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1914895 | AGTCCTAAGTGTCCC[A/G]CTGCAACATCCACAG | 7468 |
rs679323 | snp | A/G | 0.095 | 0.19615 | intron-variant | WHSC1 | GRCh38.p7 | 4:1913167 | aggtgaccagaagac[A/G]agagtgtgagccctc | 7468 |
rs1075781 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | WHSC1 | GRCh38.p7 | 4:1969958 | GTGGTTCCTACTCTC[C/T]AGTGTGTTCCTTGAG | 7468 |
rs1076134 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WHSC1 | GRCh38.p7 | 4:1952930 | AGACACTCCCATAAG[G/T]GAGGTGCTGCTGTGG | 7468 |
rs1076892 | snp | A/C/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1951261 | ACAAATTCGCTCTGC[A/C/G]TACCGGGGCCCCAGT | 7468 |
rs1079730 | snp | C/G | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886031 | TTTTGGTTGGTGAGA[C/G]CAGAGTTGTATGTAT | 7468 |
rs1132849 | snp | G/T | 0.0562649 | 0.15989 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979529 | GTGGCAGCAATGGTG[G/T]TGTAAGATTTCCTCC | 7468 |
rs1132852 | snp | A/C | 0 | 0 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1979789 | TGCTAAACCTATTTC[A/C]CAAATCACCACCGAC | 7468 |
rs1132853 | snp | G/T | 0 | 0 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981392 | GCCCTGCCCAGCTTT[G/T]TTCTGAGGACGTGGT | 7468 |
rs1133476 | snp | A/C | 0 | 0 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942186 | AATTATTACATGGTA[A/C]TACATCACCCTGAGG | 7468 |
rs1980626 | snp | A/C/T | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1937797 | ACTGTCCTGTCCCCA[A/C/T]AGCACTAGAGCAGCG | 7468 |
rs2180857 | snp | A/T | 0 | 0 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1938179 | CCGCTCTCGCATCTG[A/T]CAGGAGGGCGAGGTG | 7468 |
rs2187692 | snp | C/T | 0.00716266 | 0.059414 | utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1981829 | CATCAACTACACTCA[C/T]AGGATCAAGATATTT | 7468 |
rs2236997 | snp | A/G | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1922773 | tctactaaaaatata[A/G]aaattagttgggcat | 7468 |
rs2754197 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1894899 | ttcagtttgagaaga[G/T]gaaaaagttctggag | 7468 |
rs2759718 | snp | A/C | | | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893534 | aaaaaacaaaAAAAA[A/C]AAAAAGAGGCAAAAT | 7468 |
rs3135122 | snp | A/G | 0.432357 | 0.171014 | intron-variant | WHSC1 | GRCh38.p7 | 4:1961370 | ACCCGGACAAGCAGA[A/G]CCTCAGGGTGCCTGG | 7468 |
rs3135148 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1934875 | tatatatatatatat[A/T]ttttttttttttttt | 7468 |
rs3197006 | snp | A/G | 0.0204249 | 0.0989712 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1942537 | AACACATACAATGAA[A/G]AAAACAGATAACAAA | 7468 |
rs3216203 | in-del | -/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1910244 | CAACCtttttttttt[-/T]cgagacagtctttct | 7468 |
rs3216204 | in-del | -/A | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1935881 | aaaacaaacaaaaaa[-/A]CCCCCAAACACCATA | 7468 |
rs3762937 | snp | A/C | 0.0685596 | 0.171987 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891862 | ACTCCATCTCAAAAA[A/C]AAAAAAAAACAAAAA | 7468 |
rs3792716 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | WHSC1 | GRCh38.p7 | 4:1933629 | TCGATCTCCTGACCT[C/T]GTGATCCACCCACCT | 7468 |
rs4299658 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | WHSC1 | GRCh38.p7 | 4:1920861 | caacatgaaaccctg[C/T]ctctaaaaaaaaaaa | 7468 |
rs4318713 | snp | C/T | 0.231482 | 0.249313 | intron-variant | WHSC1 | GRCh38.p7 | 4:1879375 | AGGCGCCCGCCACCA[C/T]GCCCGGCTAATTTTT | 7468 |
rs4865478 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | WHSC1 | GRCh38.p7 | 4:1914227 | gagaccagcctggcc[A/G]acatagcaaaacccc | 7468 |
rs4865481 | snp | G/T | 0.499609 | 0.0139722 | intron-variant | WHSC1 | GRCh38.p7 | 4:1872637 | TCACAGGGTCTGCGC[G/T]CTCTCTCTCTCTCTC | 7468 |
rs5855722 | in-del | -/AA | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1873799 | ACCATCTTAGCACTT[-/AA]CTTTTAAGTTCTTGC | 7468 |
rs6599402 | snp | A/G | 0.232359 | 0.249377 | intron-variant | WHSC1 | GRCh38.p7 | 4:1886388 | atttttgtattttta[A/G]tagagacagggtttc | 7468 |
rs6814150 | snp | G/T | 0.186105 | 0.241697 | intron-variant | WHSC1 | GRCh38.p7 | 4:1915984 | GGTACCTCCTTTCTT[G/T]TATTTTGGGCCCGTC | 7468 |
rs6814151 | snp | G/T | 0.186105 | 0.241697 | intron-variant | WHSC1 | GRCh38.p7 | 4:1915985 | GTACCTCCTTTCTTT[G/T]ATTTTGGGCCCGTCT | 7468 |
rs6814391 | snp | C/T | 0.186105 | 0.241697 | intron-variant | WHSC1 | GRCh38.p7 | 4:1916135 | TGATGCTCCTGTCAC[C/T]CTAGCACTGTGAGAT | 7468 |
rs6820307 | snp | C/T | 0 | 0 | intron-variant, utr-variant-3-prime | WHSC1 | GRCh38.p7 | 4:1946775 | ATCTGATTCCTATAC[C/T]GGATGAGCAAGGAGC | 7468 |
rs6822607 | snp | G/T | 0 | 0 | intron-variant | WHSC1 | GRCh38.p7 | 4:1882212 | TGATTGGATTGGACA[G/T]CCCTGTCTCCTTGAA | 7468 |
rs6830342 | snp | C/G | 0.239902 | 0.249796 | upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1870404 | GCTCCCTGAACCTGC[C/G]TGACAGAAAACCCAA | 7468 |
rs6853594 | snp | G/T | 0.0418186 | 0.138422 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893556 | ttgtttttttttttt[G/T]tttgttttgttttga | 7468 |
rs7377981 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | WHSC1 | GRCh38.p7 | 4:1958873 | AAGAGTGTCTTTCGC[C/T]ACCTCTTCCCTAAGA | 7468 |
rs7441707 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1934878 | aaaaaaaaaaaaaaa[A/T]atatatatatatata | 7468 |
rs7657447 | snp | G/T | 0.185155 | 0.241444 | intron-variant | WHSC1 | GRCh38.p7 | 4:1921215 | gtaatcccagcactt[G/T]gggaggctgaggcgg | 7468 |
rs7669316 | snp | A/G | 0.0962929 | 0.197165 | intron-variant | WHSC1 | GRCh38.p7 | 4:1931135 | TGATGTGGTAGGGTC[A/G]GCCTTCAGGCCTGTG | 7468 |
rs7673596 | snp | A/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1872591 | GTGTGTGTGTGTGTG[A/T]GAGAGAGAGAGAGAG | 7468 |
rs9631824 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | WHSC1 | GRCh38.p7 | 4:1874080 | ACCTTTCTAAGTAAA[C/T]AATTAATCAGCAGCA | 7468 |
rs9799374 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1878286 | ttttttttttttttg[G/T]atttttagtagagac | 7468 |
rs9993250 | snp | C/T | 0.119281 | 0.213102 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881269 | gttttgtttttgttt[C/T]tgtttttttgagacg | 7468 |
rs9996424 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | WHSC1 | GRCh38.p7 | 4:1920206 | tgtaatctcagcaca[C/T]tgggaggctaaggtg | 7468 |
rs9997044 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | WHSC1 | GRCh38.p7 | 4:1882872 | gtggggcccaacaat[A/C]tgtgttctaatgtgt | 7468 |
rs9999240 | snp | C/T | 0.115438 | 0.210697 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923684 | aaattgaagatgtgc[C/T]tttttttctcttaca | 7468 |
rs9999420 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | WHSC1 | GRCh38.p7 | 4:1923839 | CAATTAAAGTGAACT[A/C]ATTGGATGTCAAAGC | 7468 |
rs9999954 | snp | A/G | 0.188 | 0.24219 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891901 | CAAAAACGAAAAAAC[A/G]AAAAACCTCACCAGA | 7468 |
rs10000617 | snp | C/T | 0.125182 | 0.216612 | intron-variant | WHSC1 | GRCh38.p7 | 4:1881361 | tccgcctcctgggtt[C/T]acgccattctcctgc | 7468 |
rs10002574 | snp | C/T | 0.124837 | 0.216412 | intron-variant | WHSC1 | GRCh38.p7 | 4:1922023 | cgtggtgatgcgcgc[C/T]tgtaatcccagctac | 7468 |
rs10004765 | snp | C/T | 0.125182 | 0.216612 | intron-variant | WHSC1 | GRCh38.p7 | 4:1930849 | CTCTGATCTTGGAAC[C/T]GTAGGGAAGTGTGTC | 7468 |
rs10005999 | snp | G/T | 0.0114282 | 0.0747228 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893543 | CTTTTTTTGTTTttt[G/T]ttttttttttttttt | 7468 |
rs10006069 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | WHSC1 | GRCh38.p7 | 4:1959930 | cagtggcatgattgt[A/C]gttcactgcagcctc | 7468 |
rs10008627 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1891688 | aaaccccatctctat[C/G]aaaaatacaaaaata | 7468 |
rs10009780 | snp | C/T | 0.125182 | 0.216612 | intron-variant | WHSC1 | GRCh38.p7 | 4:1924811 | GCACACTTGTAGTCT[C/T]AGTTACTCAGGAAGC | 7468 |
rs10013545 | snp | C/G | 0.0391387 | 0.134304 | intron-variant | WHSC1 | GRCh38.p7 | 4:1908855 | cacaatcatagctca[C/G]tccaggctcaaactc | 7468 |
rs10019114 | snp | A/G | 0.119281 | 0.213102 | intron-variant, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893337 | gagccaggcgtggtg[A/G]tgcatgcctgtagtc | 7468 |
rs10019502 | snp | A/G | 0.119281 | 0.213102 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | WHSC1 | GRCh38.p7 | 4:1893735 | ttttttgcagagaca[A/G]gatttcgccatgttg | 7468 |
rs10021693 | snp | C/T | 0.125182 | 0.216612 | intron-variant | WHSC1 | GRCh38.p7 | 4:1903934 | agagacagggtttca[C/T]tgtgttagccaggat | 7468 |
rs10023086 | snp | C/T | 0.126219 | 0.217206 | intron-variant | WHSC1 | GRCh38.p7 | 4:1909096 | GTTATATATTTTAGT[C/T]Cttattttcttaaat | 7468 |
rs10024338 | snp | G/T | | | intron-variant | WHSC1 | GRCh38.p7 | 4:1934523 | agataaaaTACTGGG[G/T]tatatttaaatttaa | 7468 |
rs10026943 | snp | G/T | 0.125182 | 0.216612 | intron-variant | WHSC1 | GRCh38.p7 | 4:1910783 | CATGGGATTGTGGAT[G/T]TGCTGTTTTTCTACT | 7468 |
rs10027958 | snp | C/G | 0.186105 | 0.241697 | intron-variant | WHSC1 | GRCh38.p7 | 4:1926790 | TTTTAATTTTTAAAG[C/G]CTTTTCTACCTTTCC | 7468 |
rs10029255 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | WHSC1 | GRCh38.p7 | 4:1977797 | actccactcaaaaaa[A/G]aaaaaaaccaaacaa | 7468 |