SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13404 | snp | A/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157168 | AGTCCAAGATCAGGG[A/T]GCCCATCTGATGAGG | 10138 |
rs289284 | snp | C/T | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42227098 | GAGGATGGAGTTCAG[C/T]GGGCAGCGGAGCTGT | 10138 |
rs401679 | snp | A/G | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42227256 | agcctctgtccggcc[A/G]ccaccccgtctggga | 10138 |
rs701250 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | YAF2 | GRCh38.p7 | 12:42188336 | TCATTTAATTATCTT[C/G]TTTGTCCTTAGCTAT | 10138 |
rs712110 | snp | A/T | 0.0189856 | 0.0955633 | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42156796 | GGAAAAACTGAAGAA[A/T]TTCAGAACAGTTACC | 10138 |
rs712111 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | YAF2 | GRCh38.p7 | 12:42167184 | taggacaaataccta[A/C]tgcatgcggggttta | 10138 |
rs712112 | snp | A/G | 0.346147 | 0.230772 | intron-variant | YAF2 | GRCh38.p7 | 12:42168242 | GGAGTGCAATGGCGC[A/G]CTCTCAGCTCACTGC | 10138 |
rs712113 | snp | A/C | 0.0429648 | 0.14013 | intron-variant | YAF2 | GRCh38.p7 | 12:42168458 | AAGTGCTGGGATTAT[A/C]GATGTGAGCCACCAT | 10138 |
rs712114 | snp | C/T | 0.347741 | 0.230777 | intron-variant | YAF2 | GRCh38.p7 | 12:42169527 | caagcaatcctcccc[C/T]ctcagcctcccaagt | 10138 |
rs712115 | snp | A/T | 0.320575 | 0.239832 | intron-variant | YAF2 | GRCh38.p7 | 12:42169904 | aagacagagtcttgc[A/T]ctgtcacccaggctg | 10138 |
rs712116 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | YAF2 | GRCh38.p7 | 12:42172304 | AATAAAGGACAGAAG[G/T]CGTACAAAATTATAA | 10138 |
rs712117 | snp | C/G | 0.0429648 | 0.14013 | intron-variant | YAF2 | GRCh38.p7 | 12:42173202 | gctcaagagatcttt[C/G]tttctcagcctcttg | 10138 |
rs712118 | snp | C/T | 0.346811 | 0.230494 | intron-variant | YAF2 | GRCh38.p7 | 12:42187308 | ACTACAGGTGCTCAC[C/T]ACCATGCCCAGCCAA | 10138 |
rs712119 | snp | C/T | 0.346368 | 0.23068 | intron-variant | YAF2 | GRCh38.p7 | 12:42187871 | AAGTCATAAAAGACA[C/T]TGTGACTTTCATCCT | 10138 |
rs712120 | snp | C/T | 0.275197 | 0.248727 | intron-variant | YAF2 | GRCh38.p7 | 12:42189073 | ATTTTTAAACTGAGC[C/T]TAGAGTGTGTGTAGA | 10138 |
rs712121 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | YAF2 | GRCh38.p7 | 12:42189467 | TCAAATCCACAACGA[C/T]TACAATGCAAGGGCA | 10138 |
rs712122 | snp | G/T | 0.345704 | 0.230956 | intron-variant | YAF2 | GRCh38.p7 | 12:42198788 | AAAGAAGAAAAGACA[G/T]CTGAGGTGCCTTTAT | 10138 |
rs712123 | snp | A/G | 0.347914 | 0.230028 | intron-variant | YAF2 | GRCh38.p7 | 12:42198796 | AAAGACATCTGAGGT[A/G]CCTTTATTGAAGAGT | 10138 |
rs712124 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | YAF2 | GRCh38.p7 | 12:42199008 | ATTCTAAACTAGCTG[C/T]GTTTAATTTCATGTG | 10138 |
rs712125 | snp | A/T | 0.347473 | 0.230215 | intron-variant | YAF2 | GRCh38.p7 | 12:42199634 | TCTTCAAGTTTCCTG[A/T]TAGGACCATAGACTG | 10138 |
rs712126 | snp | A/G | 0.378174 | 0.214642 | intron-variant | YAF2 | GRCh38.p7 | 12:42201595 | Tcaacaacaacaaca[A/G]caacagcaacaaAAA | 10138 |
rs712127 | snp | A/G | 0.376195 | 0.215812 | intron-variant | YAF2 | GRCh38.p7 | 12:42202660 | caagaacgacactcc[A/G]tctcaaaaaatagaa | 10138 |
rs712128 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | YAF2 | GRCh38.p7 | 12:42204161 | gataatgaaaagcat[C/T]ggtgacattacagaa | 10138 |
rs712129 | snp | G/T | 0.34989 | 0.229177 | intron-variant | YAF2 | GRCh38.p7 | 12:42204374 | gcagattgaaaatat[G/T]tggggggaaaagttg | 10138 |
rs712130 | snp | A/G | 0.357024 | 0.225933 | intron-variant | YAF2 | GRCh38.p7 | 12:42207720 | acacggtgaaacccc[A/G]tctctactaaaaata | 10138 |
rs771039 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42227476 | ctgagatgtggggag[C/T]gcctctgccccgccg | 10138 |
rs796400 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42227615 | tggcaaccaccccgt[C/T]tgagaagtgaggagc | 10138 |
rs824741 | snp | C/G | 0.345925 | 0.230864 | intron-variant | YAF2 | GRCh38.p7 | 12:42165434 | ttttaaagttatcta[C/G]acctcgaatggccaa | 10138 |
rs850828 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | YAF2 | GRCh38.p7 | 12:42165957 | gagtctcacactgtc[A/G]cccaggctggagtgc | 10138 |
rs864291 | snp | A/C | 0.0433465 | 0.140692 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42158392 | ACTGTTACAAAAAAT[A/C]TTTTTGTATTTTTGT | 10138 |
rs866091 | snp | C/T | 0.346811 | 0.230494 | intron-variant | YAF2 | GRCh38.p7 | 12:42185050 | gggcttggtggcgca[C/T]ggctgtagacctagc | 10138 |
rs1057574 | snp | A/G | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42223124 | TGGGCTCTAATATTA[A/G]TTCTGTGACTGGATT | 10138 |
rs1057575 | snp | A/G | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42223001 | GTGACAGATAATGAA[A/G]GACACAGCTTTTTAC | 10138 |
rs1059360 | snp | C/T | 0.470378 | 0.11804 | synonymous-codon, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160703 | TGCATCTAGTGCTGC[C/T]TCTGCAGATCAACAC | 10138 |
rs1069644 | snp | A/G | 0.32153 | 0.239548 | intron-variant | YAF2 | GRCh38.p7 | 12:42184275 | attctgcagccccat[A/G]gatccaggagtaatt | 10138 |
rs1234113 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | YAF2 | GRCh38.p7 | 12:42192839 | AAGCATATagtcaca[C/T]gtcgcataacaacat | 10138 |
rs1238290 | snp | A/T | 0.34989 | 0.229177 | intron-variant | YAF2 | GRCh38.p7 | 12:42192137 | GGAGAATATTGAATA[A/T]GGAGAAAAATTACAT | 10138 |
rs1388795 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | YAF2 | GRCh38.p7 | 12:42197216 | AGCACGTGGCAGCAG[C/T]GACTGCTAACAAGCT | 10138 |
rs1485449 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42203002 | ATAGTTTTGGAAAAA[A/G]AAAAAGAATGAGGAG | 10138 |
rs1683193 | snp | C/G | 0.0429648 | 0.14013 | intron-variant | YAF2 | GRCh38.p7 | 12:42166182 | CCTCCCAAAGTGCTG[C/G]GATTACAGGCATGAG | 10138 |
rs1683194 | snp | A/G | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42178947 | agtcttacgtactca[A/G]aaggctgaggcggga | 10138 |
rs1683195 | snp | C/G | 0.375399 | 0.216275 | intron-variant | YAF2 | GRCh38.p7 | 12:42180066 | TGTTTCATTAACTTA[C/G]TCACTCATGAAAATG | 10138 |
rs1683196 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | YAF2 | GRCh38.p7 | 12:42181151 | TTCAGAGTGGGACAA[C/G]CTGTCCTTTGTTTGA | 10138 |
rs1826387 | snp | A/C | 0.34989 | 0.229177 | intron-variant | YAF2 | GRCh38.p7 | 12:42215775 | AAAAACACCAAAAAA[A/C]ATTAGCCAGGCATGA | 10138 |
rs1873684 | snp | A/G/T | 0.0618969 | 0.166491 | intron-variant | YAF2 | GRCh38.p7 | 12:42165503 | gagcctagctctgtc[A/G/T]cccaggctggagtgc | 10138 |
rs2100547 | snp | A/G | 0.348794 | 0.229651 | intron-variant | YAF2 | GRCh38.p7 | 12:42193687 | TTTTTGTATTTTTGT[A/G]GAGACAGGGTTTTGC | 10138 |
rs2124496 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42206713 | TAATGACAAAAAAAA[A/G]ATCACTTTTTAGGAA | 10138 |
rs2290539 | snp | C/T | 0.0528381 | 0.153711 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42159417 | ATAAAACTCTTTAAA[C/T]AGTTGTAAACAAAAA | 10138 |
rs2406567 | snp | C/G | 0.464841 | 0.127841 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157677 | CCACTATCATTTTAG[C/G]AAAGCATTTAATAAA | 10138 |
rs2406568 | snp | C/G | 0.464629 | 0.128197 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42158495 | AATTTTACACGGATT[C/G]ACTTAATCCTCCCAA | 10138 |
rs2605401 | snp | C/T | 0.378174 | 0.214642 | | | GRCh38.p7 | 12:42215405 | GACCTCATATCTACA[C/T]AAAATTGAAATTAAA | 10138 |
rs2639125 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | YAF2 | GRCh38.p7 | 12:42193732 | TGGTTTCCAACTCCT[A/G]GGCTCAAGTGATCTG | 10138 |
rs2639128 | snp | A/T | 0.0433465 | 0.140692 | intron-variant | YAF2 | GRCh38.p7 | 12:42216594 | AGGTCTCTTTTCTCA[A/T]GGTAGGCAATCTATT | 10138 |
rs3834715 | in-del | -/T | 0.0217236 | 0.101931 | intron-variant | YAF2 | GRCh38.p7 | 12:42217258 | GGGTATAATTTTTTT[-/T]ATAAGAAAATGGTTT | 10138 |
rs3990969 | in-del | -/AAAC | | | intron-variant | YAF2 | GRCh38.p7 | 12:42185198 | aacaaacaaacaaac[-/AAAC]aaaaaaACagaacta | 10138 |
rs4402364 | snp | C/T | 0.338069 | 0.233974 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239934 | GGAGAATCGCTGGAA[C/T]CCGAGAGTGAGAGGT | 10138 |
rs4417370 | snp | C/G | 0.313082 | 0.241911 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239943 | CTGGAATCCGAGAGT[C/G]AGAGGTTGCTGTGAG | 10138 |
rs4768014 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42223004 | AAAAGCTGTGTCTTT[C/T]ATTATCTGTCACTTG | 10138 |
rs6582385 | snp | C/T | 0.34989 | 0.229177 | intron-variant | YAF2 | GRCh38.p7 | 12:42214824 | GCCGGGCCAACACGG[C/T]GAAACCCCTTCTCTA | 10138 |
rs6582386 | snp | A/G | 0.400147 | 0.19989 | intron-variant | YAF2 | GRCh38.p7 | 12:42226686 | AAATAAATAAATAAT[A/G]CTAAAACGATTTATA | 10138 |
rs6582387 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | YAF2 | GRCh38.p7 | 12:42226693 | taaaTAATGCTAAAA[C/T]GATTTATACCTACAA | 10138 |
rs6582388 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | YAF2 | GRCh38.p7 | 12:42229975 | AGAGGGCTTCTTTGA[A/G]AAGTACCATATggtg | 10138 |
rs6582389 | snp | A/C | 0.347253 | 0.230308 | intron-variant | YAF2 | GRCh38.p7 | 12:42230541 | AAAGATAATGAAGAT[A/C]ATGTTAGTAGCATTC | 10138 |
rs7134225 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42196055 | ggtgaaaccccatct[C/T]tactaaagacacaaa | 10138 |
rs7134478 | snp | A/C/T | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42196224 | agagcaagaatccat[A/C/T]tggaaaaaaaaaaaa | 10138 |
rs7136148 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42221665 | TGTTTTCTTACCTAT[C/G]AAGAGGATACGAGGC | 10138 |
rs7137140 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | YAF2 | GRCh38.p7 | 12:42193108 | tcactagaggccagg[A/G]gtttgagaccagcct | 10138 |
rs7138877 | snp | A/G | 0.465892 | 0.126058 | intron-variant | YAF2 | GRCh38.p7 | 12:42188512 | TGCCTCAGCCTCCTG[A/G]GTAGCTGGGATTACA | 10138 |
rs7299729 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | YAF2 | GRCh38.p7 | 12:42177593 | gccttatctccaaat[A/G]cagtcacataggggg | 10138 |
rs7300966 | snp | A/G | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42165341 | TTTTAATAAGAGAAC[A/G]ATGAAACGACTTCAT | 10138 |
rs7302429 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42229437 | aaaaaaaaaaaaaAA[A/C]ATTTAAATATCTACA | 10138 |
rs7302687 | snp | A/G | 0.34989 | 0.229177 | intron-variant | YAF2 | GRCh38.p7 | 12:42217132 | GAGAGAATAAAATCT[A/G]TCGGCTGTGGTTTCA | 10138 |
rs7304350 | snp | C/T | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42187515 | GTGTGCTTCTATATT[C/T]TTTGTGTTCCAAGAA | 10138 |
rs7306048 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | YAF2 | GRCh38.p7 | 12:42193213 | CCACCTACTCGGGAG[A/G]CTGAGGCAGGCGAAT | 10138 |
rs7306548 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | YAF2 | GRCh38.p7 | 12:42177977 | ATAGTTTATCATCTG[C/T]TTTCCTCTACCAGAA | 10138 |
rs7311447 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42194426 | agacaggcagatcac[C/T]tgaggtcaggagttc | 10138 |
rs7315777 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42165340 | CTTTTAATAAGAGAA[C/T]AATGAAACGACTTCA | 10138 |
rs7316316 | snp | C/T | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42195837 | agcacagaaggcttt[C/T]tgattaaattaagaa | 10138 |
rs7316575 | snp | C/T | 0.335101 | 0.23507 | intron-variant | YAF2 | GRCh38.p7 | 12:42212894 | AATTGGAATAAATAT[C/T]AGAAAAGGGTCATCT | 10138 |
rs7358755 | snp | C/T | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42224145 | ATCCATTCTCAACTC[C/T]TTGTATTTACTCACT | 10138 |
rs7956016 | snp | C/T | 0.32153 | 0.239548 | intron-variant | YAF2 | GRCh38.p7 | 12:42226776 | ATTGGAAAAGCAACG[C/T]CAGGTGTCAAATAGC | 10138 |
rs7957401 | snp | G/T | 0.0437281 | 0.141251 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239501 | AACTGTGCTGTTTCT[G/T]TCCATCTTTCTAGGT | 10138 |
rs7960176 | snp | C/T | 0.380605 | 0.213172 | intron-variant, utr-variant-3-prime, utr-variant-5-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42235748 | GGATCTACAAGAGCT[C/T]AGATGTACTGGTAAA | 10138 |
rs7960285 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | YAF2 | GRCh38.p7 | 12:42167754 | ctcacatctataatc[C/T]cagcactttgggagg | 10138 |
rs7960851 | snp | A/G | 0.0626037 | 0.165477 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42209960 | tgcaccaccatgccc[A/G]gctaattttctattt | 10138 |
rs7964994 | snp | A/T | 0.0433465 | 0.140692 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42231499 | ttctttgatactaca[A/T]aaaaacacagttgtt | 10138 |
rs7965273 | snp | C/T | 0.306927 | 0.243432 | intron-variant | YAF2 | GRCh38.p7 | 12:42171538 | AGAAAGAAAGAAATA[C/T]GTTACTTGTAGAATT | 10138 |
rs7970115 | snp | A/C | 0.350327 | 0.228986 | intron-variant | YAF2 | GRCh38.p7 | 12:42175018 | catccaggcatttcc[A/C]tttcaatatatgtac | 10138 |
rs7971397 | snp | C/T | 0.00627858 | 0.0556765 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238185 | TTGTCTCCCATGGCT[C/T]GGCTATCACCGCACG | 10138 |
rs7973396 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42179816 | aaaaaaaaagaaaTC[A/C]GTAGTATTAAAAGAT | 10138 |
rs7974654 | snp | A/C | 0.476052 | 0.106772 | intron-variant | YAF2 | GRCh38.p7 | 12:42236664 | CCTTCTTTTTTAAAG[A/C]AACAGTAAGATTAGT | 10138 |
rs7974752 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | YAF2 | GRCh38.p7 | 12:42167750 | gtggctcacatctat[A/G]atcccagcactttgg | 10138 |
rs7975518 | snp | A/C | 0.400504 | 0.199621 | intron-variant | YAF2 | GRCh38.p7 | 12:42224099 | TTCATATAAGCACAG[A/C]CTTCTCCAAAAACTA | 10138 |
rs7978820 | snp | C/G | 0.330947 | 0.236533 | intron-variant | YAF2 | GRCh38.p7 | 12:42195137 | ACTATTATGGGAGAA[C/G]TCCAAAATGGATAAA | 10138 |
rs9325211 | snp | C/T | 0.422 | 0.181428 | intron-variant | YAF2 | GRCh38.p7 | 12:42226233 | TTTTTAGCTATATTA[C/T]ATCATATAAATTTCA | 10138 |
rs9668208 | snp | C/G | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42227308 | GCCGCCCATCGTCTG[C/G]GACGTGAGGAGCCCC | 10138 |
rs9668209 | snp | C/T | 0.365232 | 0.22186 | intron-variant | YAF2 | GRCh38.p7 | 12:42227311 | GCCCATCGTCTGCGA[C/T]GTGAGGAGCCCCTCT | 10138 |
rs9669083 | snp | G/T | 0.469638 | 0.128931 | intron-variant | YAF2 | GRCh38.p7 | 12:42226997 | AGCCGGGACAGTCGC[G/T]GCGCTGACGCCCGCG | 10138 |
rs9669751 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | YAF2 | GRCh38.p7 | 12:42225005 | ccaacagtgtaaaag[C/T]gttcctatttctcca | 10138 |
rs10083090 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234921 | tgaacctgggagttc[A/G]aggctgcagtgagcc | 10138 |