SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs2068 | snp | A/C/T | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124912 | ACTCCAGGTCACCTC[A/C/T]GGGTAANTGAAAGGC | 57630 |
rs2069 | snp | C/G | 0.141258 | 0.225111 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169124915 | AGGACTCCAGGTCAC[C/G]TCCGGGTGAATGAAA | 57630 |
rs868050 | snp | C/T | 0.334412 | 0.235318 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169218877 | AGTAAAATTTTGCTT[C/T]AAGTAATTAGGAGTC | 57630 |
rs906321 | snp | G/T | 0.0283406 | 0.115616 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169177713 | GCAACTTGAAAGCAT[G/T]ATAGATATTTAAACA | 57630 |
rs963991 | snp | C/T | 0.102726 | 0.202016 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105889 | AGAACTCTCttcttt[C/T]tttgagacagggtct | 57630 |
rs1039704 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169267555 | AACCTCCCTATCCCA[A/G]AGTTCTCACTATCTT | 57630 |
rs1039707 | snp | C/T | 0.138886 | 0.22395 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250540 | atCAGTGAATGGTTA[C/T]ACTTGATGTATGTTG | 57630 |
rs1046583 | snp | A/C | 0 | 0 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169094805 | GAAGATGAAATCATT[A/C]CTAAATTAACCTTTT | 57630 |
rs1080160 | snp | G/T | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169104179 | CCCACACTCTCCCTA[G/T]GCACTGGCATGGGCA | 57630 |
rs1395659 | snp | C/T | 0.487621 | 0.0776941 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169208116 | CAATTCTGGGTTCAA[C/T]CTTTACGTTTCCACG | 57630 |
rs1395661 | snp | C/T | 0.364817 | 0.222075 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169172969 | AGTTTTAGAGTAATA[C/T]CTGTTCATGATAGAA | 57630 |
rs1471172 | snp | C/T | 0.470253 | 0.118274 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169096709 | TTTGAATCGCCTTAA[C/T]CAAAATCTCTTTCTT | 57630 |
rs1507166 | snp | C/T | 0.113685 | 0.209567 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254173 | AATTCCAAGGTCCAT[C/T]GGAACACATTCACAT | 57630 |
rs1507167 | snp | C/T | 0.499879 | 0.0077866 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169233647 | ATAACTTCCATTTTT[C/T]CAGAAGCCAAACAAC | 57630 |
rs1507168 | snp | C/T | 0.499801 | 0.00998203 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217293 | CCACAATTGCCTTTA[C/T]CTCTGGGTCAGGTCT | 57630 |
rs1507169 | snp | C/T | 0.0905309 | 0.192535 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169217292 | CACAATTGCCTTTAC[C/T]TCTGGGTCAGGTCTA | 57630 |
rs1507171 | snp | A/G | 0.24134 | 0.24985 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169267113 | AATTTTGGGAGCTTA[A/G]CAGTTCAGATAAATG | 57630 |
rs1542978 | snp | A/G | 0.102726 | 0.202016 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169160248 | ACCATATTGTGGGTC[A/G]TTTGGAATTTTACAG | 57630 |
rs1551613 | snp | A/G | 0.499908 | 0.00678851 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169097685 | tagggccatcttgga[A/G]gttggctaccataCA | 57630 |
rs1827994 | snp | A/G | 0.395087 | 0.203592 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166536 | GGTTTTGTAACAGTT[A/G]CAAGAACTTTCTCCT | 57630 |
rs1848195 | snp | A/G | 0.431029 | 0.17242 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202840 | TTGAAGACCACCTCA[A/G]CATTTATAATGGTAA | 57630 |
rs1876396 | snp | A/G | 0.231482 | 0.249313 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169245598 | GTTTTCTCCAAGTAG[A/G]CAAGAATGGGATCTT | 57630 |
rs1876397 | snp | A/T | 0.348794 | 0.229651 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169242126 | TCTACAAAAAAAAAA[A/T]TTTAAATTGAAATAG | 57630 |
rs1876398 | snp | C/T | 0.330016 | 0.236849 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169225481 | TTCTTGAAATGACTT[C/T]CCTTCCTCATGTCCC | 57630 |
rs1963264 | snp | A/G | 0.0948562 | 0.196037 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169248403 | tgagtgagaacatgc[A/G]gtgtttggttttctg | 57630 |
rs1976543 | snp | A/G | 0.496616 | 0.0409947 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169131495 | AATAGACTTTGGTTC[A/G]CAGGAAAAATAGAAA | 57630 |
rs1976544 | snp | C/G | 0.157972 | 0.232445 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169167366 | AGTATTAGACCCCCA[C/G]TAGCAATCTATGTAA | 57630 |
rs1976545 | snp | A/T | 0.395087 | 0.203592 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169166873 | AGATTTTTACATTGC[A/T]GATACCAATTTTGGT | 57630 |
rs1983142 | snp | C/T | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211712 | CATACATTCACACAT[C/T]TGTATCTAGGCTTTA | 57630 |
rs2009324 | snp | A/T | 0.261056 | 0.249755 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153874 | ACTTGACTCATCAGG[A/T]TTATTTACTCTGACT | 57630 |
rs2009329 | snp | A/T | 0.480302 | 0.0972668 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153979 | GATGCATGAAAAGGG[A/T]TTACTATATTTTTGT | 57630 |
rs2009747 | snp | C/T | 0.156319 | 0.231784 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220163 | ATAACAAAACTATTC[C/T]TTGCATTAGTTACTC | 57630 |
rs2054223 | snp | C/T | 0.108755 | 0.206276 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169101554 | ggcattgagtacatt[C/T]atgttgtcatacaac | 57630 |
rs2063126 | snp | C/G | 0.22263 | 0.248497 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169151580 | ACTTCCTCTGACAGA[C/G]TTTCTCTCACCTCAT | 57630 |
rs2068899 | snp | C/T | 0.132751 | 0.2208 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169269599 | TAAGAAATTATGTTC[C/T]TTATTGCACTTCATA | 57630 |
rs2135776 | snp | C/T | 0.159622 | 0.233092 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169197818 | TTCTTCAGCGCTTTT[C/T]GGTTAGAATAATATT | 57630 |
rs2135778 | snp | A/G | 0.105924 | 0.204309 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161131 | TCTCTCCTTTTAAGC[A/G]TCCCTTTCATGTGTA | 57630 |
rs2174749 | snp | C/G | 0.0944967 | 0.195752 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169250610 | CTGTATCCCCAGCAG[C/G]TAGAACACTGCCTAG | 57630 |
rs2245118 | snp | A/T | 0.463989 | 0.129263 | utr-variant-3-prime | SH3RF1 | GRCh38.p7 | 4:169094786 | AATTAACCTTTTTTT[A/T]AAAAAAAAACAATGT | 57630 |
rs2331606 | snp | G/T | 0.125182 | 0.216612 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169218308 | TATAATATAAATATA[G/T]AATATAGAATATAGA | 57630 |
rs2331607 | snp | C/T | 0.498034 | 0.0312882 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169218327 | ATAGAATATAGAATA[C/T]AGATTATAGAATATA | 57630 |
rs2331608 | snp | C/T | 0.234982 | 0.249549 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232146 | TGTGGCCAGTACGAG[C/T]GCTAGTAAGCACCTG | 57630 |
rs2331609 | snp | C/T | 0.401924 | 0.198543 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169232203 | ACAGGCTCTTGGAGA[C/T]AGTGCCAAAATTTTT | 57630 |
rs2331612 | snp | A/T | 0 | 0 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169254603 | GATGGGGGAAACTGA[A/T]TTTATCTAAGGAAAA | 57630 |
rs2331647 | snp | A/G | 0.113685 | 0.209567 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169253221 | TTCTAAAGTTACCAA[A/G]CCTTCCTAGCATGTT | 57630 |
rs2446173 | snp | C/T | 0.499563 | 0.0147699 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105648 | cctgtaatcgcagca[C/T]tttgggaggctgggg | 57630 |
rs2446174 | snp | C/T | 0.386884 | 0.209196 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105758 | GGGAATGGTGGCACA[C/T]GCTTGTGGTCCCAGC | 57630 |
rs2608850 | snp | G/T | 0.104504 | 0.2033 | | | GRCh38.p7 | 4:169100423 | ACCCAGGAGGCGGAG[G/T]TTGTGGTGAGCTGAG | 57630 |
rs2608851 | snp | A/G | 0.0970103 | 0.197722 | | | GRCh38.p7 | 4:169094337 | TAATGATAAAATTGC[A/G]ATTTATCACTCCTTT | 57630 |
rs2660395 | snp | C/T | 0.361263 | 0.223876 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169186778 | ACCTCGTGATCCGCC[C/T]GCCTCAGCCTCCCAA | 57630 |
rs2660396 | snp | C/T | 0.277334 | 0.248501 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169249804 | TCTTTATAAGTCACT[C/T]ATAAACATGACTGCA | 57630 |
rs2660398 | snp | A/G | 0.162581 | 0.234218 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180930 | CCCTTCAAACCCTTC[A/G]TCCGGCTAGTGCTGA | 57630 |
rs2660399 | snp | A/G | 0.0944967 | 0.195752 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169239327 | TTTTTTTTTTCCTGC[A/G]TGTCACTTGAACACT | 57630 |
rs2660400 | snp | G/T | 0.499999 | 0.000798721 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169235847 | ctaaaaacacaaaaa[G/T]tagccagtcctggtg | 57630 |
rs2660401 | snp | C/T | 0.441568 | 0.160629 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169235830 | agccagtcctggtgg[C/T]gcacacctgtaatcc | 57630 |
rs2660402 | snp | A/G | 0.499958 | 0.00459246 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169231719 | GTGATTTGGAAGGGA[A/G]CAGTAATGCATAGTG | 57630 |
rs2660403 | snp | A/G | 0.162581 | 0.234218 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180000 | TTTAGCATTACATCT[A/G]AGATGTTTGATATAT | 57630 |
rs2660404 | snp | G/T | 0.499653 | 0.0131743 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228550 | CTTTTAGAAGTGGAA[G/T]AGCGAGGCAGAAGAC | 57630 |
rs2660405 | snp | A/G | 0.499653 | 0.0131743 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169226453 | TTTTTCTTCATTATA[A/G]CATTCCATGTATTTT | 57630 |
rs2660406 | snp | A/T | 0.499653 | 0.0131743 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224704 | ctgcagtagtcttgt[A/T]cctggttacccctgc | 57630 |
rs2660407 | snp | C/T | 0.499653 | 0.0131743 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169224598 | ggtggtggtggttca[C/T]gcctgtaatcccagc | 57630 |
rs2660408 | snp | C/T | 0.118584 | 0.212673 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223694 | TTATTTGTTGATATG[C/T]TTGCCCATCACCCCA | 57630 |
rs2660409 | snp | A/G | 0.499551 | 0.0149693 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223612 | TTTAAAAAAGAAAGT[A/G]AGCTCCAAGCAATCA | 57630 |
rs2660410 | snp | A/G | 0.499776 | 0.0105807 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223241 | TCTGATCCATGCTTA[A/G]TGGCCATTGCATGTT | 57630 |
rs2660411 | snp | C/T | 0.499793 | 0.0101816 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223224 | GGCCATTGCATGTTA[C/T]TATCCCTACATGTTG | 57630 |
rs2660412 | snp | C/T | 0.499891 | 0.00738737 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169223004 | CCGCCTTGTGAAGAG[C/T]TGCAGCTGGGCAAAC | 57630 |
rs2660413 | snp | A/G | 0.0905309 | 0.192535 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169220715 | GCTTTGTGTTGCATG[A/G]TGGTAACTATAGAGT | 57630 |
rs2660414 | snp | A/G | 0.130008 | 0.219321 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169216467 | CAACAACAATAAAAG[A/G]AGCAAGAACAGTTAT | 57630 |
rs2660415 | snp | A/T | 0.443195 | 0.158668 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169213589 | agatttggtggtgac[A/T]ttttagatgcattct | 57630 |
rs2660416 | snp | A/G | 0.137867 | 0.223442 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212760 | catttttccaaaacc[A/G]tggcatagaacacca | 57630 |
rs2660417 | snp | G/T | 0.499933 | 0.00579035 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212215 | cagctgggcatggtg[G/T]cacatgcttgtaatc | 57630 |
rs2660418 | snp | C/T | 0.119281 | 0.213102 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169212087 | ataagagcaaaactc[C/T]gtctcaaaaaaaaaa | 57630 |
rs2660419 | snp | A/G | 0.499992 | 0.00199679 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169211169 | TCTTCTTTGGAGAAT[A/G]GGTCATAATACTAAA | 57630 |
rs2660420 | snp | A/G | 0.119281 | 0.213102 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169209287 | TTTTTTTTTTTTTTC[A/G]GACAGGGTCTTGTTC | 57630 |
rs2660421 | snp | C/T | 0.499995 | 0.00159744 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169206572 | TGTTTCTTGACTTCA[C/T]TTATTTAAAGTGAAT | 57630 |
rs2660422 | snp | G/T | 0.499987 | 0.00259581 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202194 | ACCAAGAACACGAAG[G/T]AGGCCCTTAATAAAT | 57630 |
rs2660423 | snp | A/T | 0.162909 | 0.23434 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199622 | gtgaatgcgcaaaaa[A/T]aaaaaaaTAAATAAA | 57630 |
rs2660424 | snp | A/C | 0.162581 | 0.234218 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199744 | aacaatttaaaaaga[A/C]agacaataaaagaga | 57630 |
rs2660425 | snp | A/G | 0.499995 | 0.00159744 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199799 | acaaatataaataaa[A/G]tattaaggtaaggtg | 57630 |
rs2660426 | snp | A/G | 0.499995 | 0.00159744 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169193705 | GTGACTGGCAGAGCT[A/G]TGTGGTGAGACCTTA | 57630 |
rs2660427 | snp | C/T | 0.49999 | 0.00219646 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169189748 | TGAAGAAATTAAACT[C/T]TGGGGATTCGAGCAA | 57630 |
rs2660428 | snp | A/G | 0.478188 | 0.10213 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169175041 | agtgggctatttacc[A/G]acattggggaaaact | 57630 |
rs2660429 | snp | C/T | 0.479177 | 0.0998894 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169174353 | AGTTTTggcctggca[C/T]gatggctcacgccaa | 57630 |
rs2660430 | snp | A/G | 0.49621 | 0.0433651 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169162057 | TCGCAAGTAGTTGGG[A/G]CTGTAGGCGCACCAC | 57630 |
rs2660431 | snp | C/T | 0.102014 | 0.201495 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169161890 | GCCTGACCCAAAAGA[C/T]ATTTTTAAAAAATTG | 57630 |
rs2660432 | snp | A/G | 0.496279 | 0.0429702 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169154020 | TTTTAGGTATTATCA[A/G]TATTACATGCTGATA | 57630 |
rs2660433 | snp | C/G | | | intron-variant | SH3RF1 | GRCh38.p7 | 4:169153003 | CCTGTAGTAGAATCT[C/G]TGGGTCAGAGGTTCA | 57630 |
rs2706711 | snp | A/T | 0.102014 | 0.201495 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169198603 | AAATACATCAAATGA[A/T]CTTTTTTAGAGCATC | 57630 |
rs2706712 | snp | A/T | 0.495963 | 0.0447464 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169199626 | ATGCGCAAAAAAAAA[A/T]AAATAAATAAATAAC | 57630 |
rs2706713 | snp | A/G | 0.498481 | 0.027514 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169168799 | TTCTTTGGCAATCAA[A/G]TCATCTGAGAGAAAA | 57630 |
rs2706714 | snp | A/G | 0.106987 | 0.205054 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169105025 | GCCAAAAATATGAAT[A/G]CAGGCCTCAGGTTTT | 57630 |
rs2706715 | snp | A/G | 0.49645 | 0.0419827 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169143409 | GCAACTTGCAGCGAG[A/G]CTCGTCCAAACTGAG | 57630 |
rs2706716 | snp | A/G | 0.112983 | 0.209108 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180086 | AAGAAAAAACTTGTA[A/G]TTCCAGTGCTGAACA | 57630 |
rs2706717 | snp | C/G | 0.499996 | 0.00139776 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169180510 | TTCAAAGCAAAAGTG[C/G]GGAAAGAAAAGAGAT | 57630 |
rs2706718 | snp | A/G | 0.0944967 | 0.195752 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169247051 | TTTAATGCCTTAACT[A/G]CTTTTGATTTATGGT | 57630 |
rs2706721 | snp | A/G | 0.499992 | 0.00199679 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169201274 | CTGGCTTTAACAATT[A/G]ACGAATACTTATTCT | 57630 |
rs2706722 | snp | C/G | 0.49975 | 0.0111793 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169202564 | TATAATTAGTATTTG[C/G]GTTAATAACACAGTG | 57630 |
rs2706723 | snp | A/G | 0.499997 | 0.00119808 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169185974 | GGGGAGGAAGCAGGC[A/G]GTGGAGAGTGTATGG | 57630 |
rs2706724 | snp | C/T | 0.49962 | 0.0137727 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169228948 | TGTTTGTTTGTTTTT[C/T]GAAGAACAGAATTTT | 57630 |
rs2706725 | snp | A/G | 0.499598 | 0.0141716 | intron-variant | SH3RF1 | GRCh38.p7 | 4:169227869 | TGAATTGAAAAATGC[A/G]ATAAACTCTGTTCTC | 57630 |