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 |
rs10160853 | snp | G/T | 0.168135 | 0.236216 | intron-variant | YAF2 | GRCh38.p7 | 12:42216042 | CCAATGTTTTGGGAT[G/T]TTTTGTTGTTAATTC | 10138 |
rs10459290 | snp | G/T | 0.462472 | 0.13174 | intron-variant | YAF2 | GRCh38.p7 | 12:42219488 | GGACATGAGAGTTCA[G/T]TAAGCTCATTCAGAG | 10138 |
rs10492386 | snp | C/T | 0.330947 | 0.236533 | intron-variant | YAF2 | GRCh38.p7 | 12:42196422 | AACCAGTACATGAAA[C/T]GATTTGCAAGCCATG | 10138 |
rs10492387 | snp | C/T | 0.331411 | 0.236373 | intron-variant | YAF2 | GRCh38.p7 | 12:42197093 | AATTTTTTCGAAAAT[C/T]AGTGTCATGACAACA | 10138 |
rs10492388 | snp | C/T | 0.465578 | 0.126594 | intron-variant | YAF2 | GRCh38.p7 | 12:42214199 | ACTATGCACTAGTCT[C/T]TGCTCAATGTAAAAC | 10138 |
rs10506175 | snp | A/G | 0.16846 | 0.236329 | intron-variant | YAF2 | GRCh38.p7 | 12:42197127 | AGAACAAACTAGAGC[A/G]CAGAAAATACAAGTA | 10138 |
rs10547916 | in-del | -/AAGC | 0.0310518 | 0.120672 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232772 | GATGATAGTTGGTTT[-/AAGC]TTCTTTCAGAATGTG | 10138 |
rs10630689 | in-del | -/AC | 0.336843 | 0.246669 | intron-variant | YAF2 | GRCh38.p7 | 12:42236567 | AATAAAATTCTGTAA[-/AC]AGTGTTTTTTAAAAA | 10138 |
rs10708373 | in-del | -/A | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42171510 | CCATCTCTTTAAATT[-/A]AAAAAAAAAGAAAGA | 10138 |
rs10785332 | snp | A/G | 0.331179 | 0.236453 | intron-variant | YAF2 | GRCh38.p7 | 12:42167666 | CTTAGCTCAATGTTG[A/G]AAAATATAAATAGCA | 10138 |
rs10785333 | snp | A/G | 0.463881 | 0.12944 | intron-variant | YAF2 | GRCh38.p7 | 12:42192668 | TATTAGAGTAGCCCA[A/G]AAAAGAGATGGTGGC | 10138 |
rs10785334 | snp | A/G | 0.475877 | 0.107142 | intron-variant | YAF2 | GRCh38.p7 | 12:42226575 | AGGCTAAGGTGGGGG[A/G]ACCACTTCAACCTGG | 10138 |
rs10880259 | snp | C/T | 0.465788 | 0.126237 | intron-variant | YAF2 | GRCh38.p7 | 12:42164201 | ACTGTATTTGTCAGA[C/T]ATGATATTCACCAAT | 10138 |
rs10880260 | snp | A/G | 0.465892 | 0.126058 | intron-variant | YAF2 | GRCh38.p7 | 12:42167596 | ATTAAAACAATACAC[A/G]TATCCTGTAACTAAT | 10138 |
rs10880261 | snp | C/T | 0.465473 | 0.126772 | intron-variant | YAF2 | GRCh38.p7 | 12:42180020 | TGGAGGACTTACTAG[C/T]ACAAAGTATTTTTCC | 10138 |
rs10880263 | snp | C/G | 0.304188 | 0.244057 | intron-variant | YAF2 | GRCh38.p7 | 12:42186410 | ATATGGTATATAAGG[C/G]TTGATCAAGAAAATA | 10138 |
rs10880264 | snp | C/T | 0.463774 | 0.129618 | intron-variant | YAF2 | GRCh38.p7 | 12:42192733 | AATGGATTTAAAGAT[C/T]TTGGTCAAGGTAGTA | 10138 |
rs10880268 | snp | C/T | 0.465158 | 0.127307 | intron-variant | YAF2 | GRCh38.p7 | 12:42205320 | TATTTCCGGAATCAA[C/T]TGCAAACAACCAGCT | 10138 |
rs10880269 | snp | C/T | 0.463989 | 0.129263 | intron-variant | YAF2 | GRCh38.p7 | 12:42212333 | TATATTCATCATATT[C/T]ATTTTAATGTGCCAC | 10138 |
rs10880270 | snp | A/G | 0.277778 | 0.248452 | intron-variant | YAF2 | GRCh38.p7 | 12:42218185 | ATCAGGCTACTAGGA[A/G]ACACACACACACACA | 10138 |
rs10880271 | snp | A/C | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42218187 | CAGGCTACTAGGAAA[A/C]ACACACACACACACA | 10138 |
rs10880272 | snp | G/T | 0.456332 | 0.141164 | intron-variant | YAF2 | GRCh38.p7 | 12:42223807 | GCATGTTCTCACTCA[G/T]AAGTGGGAGTTGAAC | 10138 |
rs10880273 | snp | A/G | 0.465158 | 0.127307 | intron-variant | YAF2 | GRCh38.p7 | 12:42224728 | TTTTTACAGCTGCAT[A/G]GTATTCCATGGTGTA | 10138 |
rs10880274 | snp | C/T | 0.307176 | 0.243374 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233484 | ACAGACTATCCTTAA[C/T]ATTTAATATTTCATT | 10138 |
rs10880275 | snp | C/T | 0.33875 | 0.233717 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238949 | ACTTCCTCTAGGCTA[C/T]ATAATTAGAAAATGA | 10138 |
rs11181354 | snp | C/G | 0.0543475 | 0.155628 | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42157037 | AAAAGAGGTAAGTAG[C/G]AGAGCAAAAAAGTAT | 10138 |
rs11181355 | snp | A/G | 0.0543475 | 0.155628 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42158044 | AGTTCATGAAACAGA[A/G]AAAAACATGTACCCT | 10138 |
rs11181356 | snp | A/G | 0.304188 | 0.244057 | intron-variant | YAF2 | GRCh38.p7 | 12:42163787 | AGCTAAAGAGCTTTC[A/G]CTGAAGGTAGGAGGA | 10138 |
rs11181357 | snp | A/C | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42165060 | accctgtcttctgga[A/C]caaaaaaaaaaaaaa | 10138 |
rs11181358 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | YAF2 | GRCh38.p7 | 12:42169027 | ACTCCTCCCTTAATC[C/T]CTTGTTTACTTGCTC | 10138 |
rs11181359 | snp | C/T | 0.331642 | 0.236293 | intron-variant | YAF2 | GRCh38.p7 | 12:42169272 | ACAAAGGTTCTACTT[C/T]CTTATTCCTCTTCCT | 10138 |
rs11181360 | snp | A/G | 0.167484 | 0.23599 | intron-variant | YAF2 | GRCh38.p7 | 12:42170018 | TGGTACCACAGGCAC[A/G]CATCACCACACCTGG | 10138 |
rs11181361 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42170605 | acttgatcctaggag[A/T]tcgagacctgcctgg | 10138 |
rs11181362 | snp | C/T | 0.168135 | 0.236216 | intron-variant | YAF2 | GRCh38.p7 | 12:42170675 | ACAAACAAAAAACTA[C/T]ACACACACACACACA | 10138 |
rs11181363 | snp | C/T | 0.245631 | 0.249962 | intron-variant | YAF2 | GRCh38.p7 | 12:42172480 | GATGTCATACAATTT[C/T]ATATAAGCCAACATG | 10138 |
rs11181364 | snp | C/T | 0.464309 | 0.12873 | intron-variant | YAF2 | GRCh38.p7 | 12:42173998 | CTCCAGGACACACTC[C/T]TGCCACTGACCTCCT | 10138 |
rs11181365 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | YAF2 | GRCh38.p7 | 12:42174642 | TCAGGCCTTGCCCTA[A/G]AACTAGGGTGATTTT | 10138 |
rs11181366 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42176318 | TAGAGATGGGGTTTC[A/G]CCATGCTGGCCAGAC | 10138 |
rs11181367 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42176324 | TGGGGTTTCACCATG[C/T]TGGCCAGACTGGTCT | 10138 |
rs11181368 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42176340 | TGGCCAGACTGGTCT[C/T]AAACTTCTGGCCTCA | 10138 |
rs11181369 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42176384 | CCTCAGCCACCCAAA[C/G]TGCTGGGATTACAGG | 10138 |
rs11181371 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | YAF2 | GRCh38.p7 | 12:42182806 | AGCATCCTAAATGAT[A/C]ATATATAATTTCTAG | 10138 |
rs11181372 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | YAF2 | GRCh38.p7 | 12:42189082 | CTGAGCTTAGAGTGT[C/G]TGTAGAATTTCAACA | 10138 |
rs11181373 | snp | A/G | 0.168785 | 0.236441 | intron-variant | YAF2 | GRCh38.p7 | 12:42194397 | GCCTGTAATCCTAAC[A/G]GTTCGGGAGGCTGAG | 10138 |
rs11181374 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | YAF2 | GRCh38.p7 | 12:42195202 | TGTCCAAGTTCTCTG[C/T]AAATGAGGAACAATA | 10138 |
rs11181375 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | YAF2 | GRCh38.p7 | 12:42195252 | TTTGACTCATGAATC[A/G]ATCTAATCAATGGAT | 10138 |
rs11181376 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | YAF2 | GRCh38.p7 | 12:42199727 | ACTAACCAAAGACAC[A/C]GAATACGGTAATACT | 10138 |
rs11181377 | snp | A/G | 0.021333 | 0.101051 | intron-variant | YAF2 | GRCh38.p7 | 12:42204176 | TGGTGACATTACAGA[A/G]AAGTGTGAACCTTTG | 10138 |
rs11181378 | snp | C/T | 0.464203 | 0.128908 | intron-variant | YAF2 | GRCh38.p7 | 12:42206856 | TTCTCTTTAAAACAC[C/T]TTCTCCTCATCTTTT | 10138 |
rs11181380 | snp | A/T | 0.460589 | 0.13473 | intron-variant | YAF2 | GRCh38.p7 | 12:42222238 | AAAGAAAAAAACACT[A/T]AGGTTTCACCAACTC | 10138 |
rs11181381 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42229204 | TTGTTAAACAGATGC[C/T]TGAAGGCAGCATGCT | 10138 |
rs11181383 | snp | C/T | 0.307671 | 0.243257 | intron-variant | YAF2 | GRCh38.p7 | 12:42236330 | TTTAGCAAATACTTT[C/T]TTTCTTTTTGGAATG | 10138 |
rs11181384 | snp | G/T | 0.264084 | 0.249603 | intron-variant | YAF2 | GRCh38.p7 | 12:42236615 | TAGAAATCTAACGTC[G/T]ACTGAATATTTGTAT | 10138 |
rs11352121 | in-del | -/A | 0.444444 | 0.157135 | intron-variant | YAF2 | GRCh38.p7 | 12:42171800 | CTCTACAGAAAATAC[-/A]AAAAAAAAAAAAAAT | 10138 |
rs11419731 | in-del | -/G | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42213062 | AAGATGTCATTAAGA[-/G]GCCAGGCACGGTGGC | 10138 |
rs11609358 | snp | A/C | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42192315 | gagatcaagaccagc[A/C]tgggcaacacagcaa | 10138 |
rs11610832 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42169946 | tacaatcacaactca[C/G]tacagcctcaacctt | 10138 |
rs11829542 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | YAF2 | GRCh38.p7 | 12:42217758 | GGAAACAAATATAAA[A/G]TATCTTCAATACACT | 10138 |
rs11829883 | snp | A/G | 0.330947 | 0.236533 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239885 | gctgtggtggcgggc[A/G]cctgtaatctcagct | 10138 |
rs11830248 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | YAF2 | GRCh38.p7 | 12:42197831 | GGGATACATGGATAA[C/T]TAGTATTAGAAGTTA | 10138 |
rs11830568 | snp | C/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233234 | ACACCTATGAGAAAC[C/T]TAAAGGACTGTTATA | 10138 |
rs11831168 | snp | A/G | 0.331642 | 0.236293 | intron-variant | YAF2 | GRCh38.p7 | 12:42164921 | CAAAAAAAATACAGA[A/G]ATTGGCCAGTAAAGG | 10138 |
rs11832197 | snp | A/G | 0.330947 | 0.236533 | intron-variant | YAF2 | GRCh38.p7 | 12:42218375 | ATGGTTTGTCTGCTC[A/G]TAAATGTTATATCTT | 10138 |
rs12049942 | snp | A/G | 0.463774 | 0.129618 | intron-variant | YAF2 | GRCh38.p7 | 12:42193250 | aactggggaggcgga[A/G]gctgcagtgaaccga | 10138 |
rs12227048 | snp | C/G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42196053 | atggtgaaaccccat[C/G/T]tctactaaagacaca | 10138 |
rs12228912 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42224540 | ctagccccccacccc[A/G]cgacaggcccccgtg | 10138 |
rs12228932 | snp | A/G | 0.331411 | 0.236373 | intron-variant | YAF2 | GRCh38.p7 | 12:42164538 | TAAGATGAAAGAAAG[A/G]AAAGAAAGAAAAAGA | 10138 |
rs12297435 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | YAF2 | GRCh38.p7 | 12:42181414 | GCCCCTTTCATCCTG[C/T]GTCTCCACTGCCTTT | 10138 |
rs12298116 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | YAF2 | GRCh38.p7 | 12:42191596 | TTTCTCTGAATTTTT[C/T]CTTGTTTTCCTTCTT | 10138 |
rs12298117 | snp | C/G | 0.0352966 | 0.128072 | intron-variant | YAF2 | GRCh38.p7 | 12:42191597 | TTCTCTGAATTTTTC[C/G]TTGTTTTCCTTCTTT | 10138 |
rs12298249 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | YAF2 | GRCh38.p7 | 12:42209490 | gatggcttgtgccca[A/G]gaggcagaagttgca | 10138 |
rs12300049 | snp | A/G | | | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42210316 | GACAAAATTTGGGGG[A/G]AAAAAAAATCTCAGG | 10138 |
rs12300611 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | YAF2 | GRCh38.p7 | 12:42164408 | TATATGCAATTTTCA[A/G]CTACGGTCTGCCTTC | 10138 |
rs12300698 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | YAF2 | GRCh38.p7 | 12:42224745 | tattccatggtgtat[A/G]tgtgccacattttct | 10138 |
rs12300940 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | YAF2 | GRCh38.p7 | 12:42203886 | TGGGATTAGCTGTTC[C/T]GCAAAAGCATATCTA | 10138 |
rs12303887 | snp | A/G | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42212532 | TTTAAGAATAGTCTA[A/G]TAACTAACTCACCAC | 10138 |
rs12304868 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42223845 | acacatggacacagg[A/G]aggggaacatcacac | 10138 |
rs12306689 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | YAF2 | GRCh38.p7 | 12:42194539 | atcccagctacttag[A/G]aggtggaggcaggag | 10138 |
rs12308598 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | YAF2 | GRCh38.p7 | 12:42202177 | GAATGCCATTTCTAG[C/T]CTTCACCAATGTTCC | 10138 |
rs12309515 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | YAF2 | GRCh38.p7 | 12:42162800 | ATGTAAAGCAGATAT[C/G]AGGAGATGGATAATG | 10138 |
rs12310090 | snp | C/G | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42178273 | gtccttttaaaatta[C/G]tatacttgggccccc | 10138 |
rs12310800 | snp | A/T | 0.0352966 | 0.128072 | intron-variant | YAF2 | GRCh38.p7 | 12:42174205 | tttctatactcactc[A/T]atacttttcccactc | 10138 |
rs12311533 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42175676 | ggtcaaaagattgag[A/C]ccatcctggccaacg | 10138 |
rs12312003 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42209318 | cctgtaatcccaaca[C/T]ttagggaggccaagg | 10138 |
rs12312515 | snp | C/G | 0.168785 | 0.236441 | intron-variant | YAF2 | GRCh38.p7 | 12:42197739 | ACATTTATATAATCA[C/G]ACTCCAAATAATCTT | 10138 |
rs12312552 | snp | A/G | 0.0103887 | 0.0713191 | synonymous-codon, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160664 | TCCTCTCTCTGTGTT[A/G]TCAGAGCTAGAGCCG | 10138 |
rs12312690 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | YAF2 | GRCh38.p7 | 12:42175112 | gtaatggcccaaaac[C/T]gaaaataacccaaat | 10138 |
rs12313439 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | YAF2 | GRCh38.p7 | 12:42236817 | TCAAGGAGCTCGATA[A/G]CTAAGTGCTGACAGA | 10138 |
rs12313448 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | YAF2 | GRCh38.p7 | 12:42203021 | TTCCAAAACTATCTT[C/G]GTTATTCTTGAACCT | 10138 |
rs12313898 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | YAF2 | GRCh38.p7 | 12:42201522 | CCGAATATTAAAGAC[A/G]TTGTGTGTGTCTCCT | 10138 |
rs12314028 | snp | C/T | 0.00366351 | 0.0426419 | intron-variant | YAF2 | GRCh38.p7 | 12:42210537 | AGACATGCTTCAGTG[C/T]ACTTGCTTACCTTCC | 10138 |
rs12315471 | snp | C/T | 0.168135 | 0.236216 | intron-variant | YAF2 | GRCh38.p7 | 12:42186600 | GAGAATCGCTCGAAC[C/T]CAGGAGGTGGAGGTT | 10138 |
rs12317772 | snp | C/G | 0.171148 | 0.237239 | intron-variant | YAF2 | GRCh38.p7 | 12:42230057 | aggtcaggagatgga[C/G]accatcctggccaac | 10138 |
rs12318401 | snp | C/T | 0.168785 | 0.236441 | intron-variant | YAF2 | GRCh38.p7 | 12:42178113 | ATGTGCAAAAATATG[C/T]ACATCTATTTTGTAT | 10138 |
rs12319084 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | YAF2 | GRCh38.p7 | 12:42209684 | CATAAATTTTACAAT[A/G]TAAGTATTTACTTCA | 10138 |
rs12320539 | snp | A/T | 0.0352966 | 0.128072 | intron-variant | YAF2 | GRCh38.p7 | 12:42179573 | ggtgggcaaatcatt[A/T]gagctcaggagtttg | 10138 |
rs12321515 | snp | A/C/G | 0.02762 | 0.114583 | intron-variant | YAF2 | GRCh38.p7 | 12:42207846 | cagtgagccgagatc[A/C/G]tgccactgcactcca | 10138 |
rs12322316 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | YAF2 | GRCh38.p7 | 12:42162306 | TCACCATGCTCTTTT[A/G]ACCCTGGAGATCTGC | 10138 |
rs12368081 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42211903 | aaaatacaaaaatta[A/G]ccgggtgtagtggca | 10138 |
rs12368082 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42211913 | aattagccgggtgta[A/G]tggcaggtgcctata | 10138 |
rs12370778 | snp | A/T | 0.495234 | 0.0485822 | intron-variant | YAF2 | GRCh38.p7 | 12:42205894 | TTTGTTGTGATTTAG[A/T]TCTAATTATTTTGTA | 10138 |
rs12371615 | snp | C/G | 0.465473 | 0.126772 | intron-variant | YAF2 | GRCh38.p7 | 12:42170187 | ATGTTATGTGTTTTT[C/G]ATAAGTCAGTCAGTC | 10138 |
rs12385814 | snp | G/T | 0.0352966 | 0.128072 | intron-variant | YAF2 | GRCh38.p7 | 12:42211527 | ggatcacctgaggtt[G/T]ggagttcaagaccag | 10138 |
rs12424199 | snp | A/T | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42167718 | GAAAAGCTGTTGAAA[A/T]TTTCTggccaggctc | 10138 |
rs12424596 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | YAF2 | GRCh38.p7 | 12:42207754 | aaattagccgggcgt[A/C]gtggcgggcgcctgt | 10138 |
rs12425106 | snp | A/G | 0.0788843 | 0.182262 | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42156641 | TGTCCTTCATTGCCT[A/G]TGATAGGAGTGGGGC | 10138 |
rs12579560 | snp | C/T | 0.329084 | 0.237162 | intron-variant | YAF2 | GRCh38.p7 | 12:42174963 | AAAGGCATACATAAA[C/T]CCCTCACATTGAAAC | 10138 |
rs12580641 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42229399 | tgagaaacacccaag[A/C]attatcaataaaaaa | 10138 |
rs12582150 | snp | C/T | 0 | 0 | intron-variant, nc-transcript-variant, missense | YAF2 | GRCh38.p7 | 12:42212447 | CTAAATAATCACCTC[C/T]TTCCTTCAAGAAACT | 10138 |
rs12582890 | snp | A/G | 0.331411 | 0.236373 | intron-variant | YAF2 | GRCh38.p7 | 12:42172778 | TAAATCAAATATGGT[A/G]TATATTCATAAAATG | 10138 |
rs12809735 | snp | A/T | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42174653 | cctagaactaGGGTG[A/T]TTTTTTTATGCATGC | 10138 |
rs12810114 | snp | A/G | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42174855 | AATAACACTTAAGGA[A/G]AAACTAGATTATGAC | 10138 |
rs12814758 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42174686 | AAAGCACTCCTCTTG[G/T]TGACCTCATTCAGTC | 10138 |
rs12816470 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42175765 | aaaaaaaaaaaaaaa[A/T]aaaaaTTAAAACAGG | 10138 |
rs12821924 | snp | G/T | 0 | 0 | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42156767 | TTTTATTCTGATCAG[G/T]GATTTTTGTCATTGG | 10138 |
rs12821944 | snp | G/T | | | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42156789 | TGTCATTGGTAACTG[G/T]TCTGAATTTCTTCAG | 10138 |
rs12822090 | snp | G/T | 0 | 0 | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42156823 | TTCCTACATTCTTTG[G/T]TCCAGACAACTGAAG | 10138 |
rs12823187 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42222548 | GAAAGCACTCTGAAC[A/C]CAGTAAAGCACTATA | 10138 |
rs12833861 | snp | C/T | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42174668 | ATTTTTTTATGCATG[C/T]TAAAAGCACTCCTCT | 10138 |
rs17091009 | snp | A/G | 0.0197687 | 0.0974348 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157543 | CCATTTACCATTAAT[A/G]CAGAGGCTACATTCT | 10138 |
rs17091018 | snp | A/G | 0.330947 | 0.236533 | intron-variant | YAF2 | GRCh38.p7 | 12:42173253 | CAAACGGGGCTCCAC[A/G]GTCTATATGTATTTA | 10138 |
rs17091023 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | YAF2 | GRCh38.p7 | 12:42195819 | CTAAGCAGATCCTAC[A/G]GGAGCACAGAAGGCT | 10138 |
rs17091030 | snp | A/C/G | 0.0197687 | 0.0974348 | intron-variant | YAF2 | GRCh38.p7 | 12:42197013 | TGTCTGTTTTGTTCA[A/C/G]TTCTCAGAAAGTACT | 10138 |
rs17091037 | snp | A/T | 0.0618563 | 0.164627 | intron-variant | YAF2 | GRCh38.p7 | 12:42197993 | AATATGTTCACTCTC[A/T]AATAGTATCTACTAG | 10138 |
rs17091040 | snp | G/T | 0.0622301 | 0.165053 | intron-variant | YAF2 | GRCh38.p7 | 12:42198047 | GTTAATTTGAAAACC[G/T]CTAAGCAATTAGTAT | 10138 |
rs17091041 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | YAF2 | GRCh38.p7 | 12:42198746 | ATTAATAGTTAAGAT[A/G]AGAGCCCACGAACAA | 10138 |
rs17592715 | snp | C/G | 0.029116 | 0.117091 | intron-variant | YAF2 | GRCh38.p7 | 12:42200707 | CACTATCATAAGTGT[C/G]GGTAAATTAGATCAC | 10138 |
rs33934066 | in-del | -/A | 0.499368 | 0.0177603 | intron-variant | YAF2 | GRCh38.p7 | 12:42206298 | AATATGCTCTTAGTT[-/A]AAAAAAAAAAAAAAA | 10138 |
rs34014227 | in-del | -/T | 0.398714 | 0.200958 | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42157063 | AGTATCTCAATCCAC[-/T]TTTTTTTTTTTGCTA | 10138 |
rs34267272 | in-del | -/A | 0.0123036 | 0.0774623 | intron-variant | YAF2 | GRCh38.p7 | 12:42196227 | CAAGAATCCATCTGG[-/A]AAAAAAAAAAAAAAA | 10138 |
rs34273085 | in-del | -/AC/CA/CG | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42236568 | ATAAAATTCTGTAAA[-/AC/CA/CG]GTGTTTTTTAAAAAA | 10138 |
rs34274992 | in-del | -/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42169320 | GTCCTTCTCAGTCAT[-/G]CTTATATCTAAACTG | 10138 |
rs34289722 | snp | A/G | 0.295088 | 0.245901 | intron-variant | YAF2 | GRCh38.p7 | 12:42225722 | TGAGGACTCTGTTCT[A/G]TTCTATCGGTCTATA | 10138 |
rs34586316 | snp | A/C | 0.444444 | 0.157135 | intron-variant | YAF2 | GRCh38.p7 | 12:42195094 | AAACAAGAAACATAC[A/C]CAAGCAATTAAAGTA | 10138 |
rs34635473 | in-del | -/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42195608 | TATTAAAAGAGCTTA[-/G]GAGAAATGAGTCATC | 10138 |
rs34650192 | in-del | -/A | | | intron-variant | YAF2 | GRCh38.p7 | 12:42221418 | TCTACAAAAAATTTT[-/A]AAATTACCTGGGTGT | 10138 |
rs34658170 | in-del | -/T | | | intron-variant, nc-transcript-variant, frameshift-variant | YAF2 | GRCh38.p7 | 12:42212467 | TCAAGAAACTTATGA[-/T]TTTCATGATTCTTCA | 10138 |
rs34683165 | in-del | -/A | | | intron-variant | YAF2 | GRCh38.p7 | 12:42211428 | CGAGACTCTGTCTCC[-/A]AAAAAAAAAAAAAAA | 10138 |
rs34896304 | snp | A/C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42200298 | GAAACAAGGAAGAAA[A/C/G]CAGATTTGCATGTAT | 10138 |
rs34938902 | in-del | -/TAA | 0.463881 | 0.12944 | intron-variant | YAF2 | GRCh38.p7 | 12:42207470 | CACAAGATAAATTAT[-/TAA]TAATATTATACTAAA | 10138 |
rs34960536 | in-del | -/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42206664 | CTTAGACAAACTGTT[-/G]CTTTGAAAAGTTCTC | 10138 |
rs34973533 | in-del | -/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42203703 | GAACTGTCCTAAACT[-/G]CCTATCCCAATTAAA | 10138 |
rs35012592 | in-del | -/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42171910 | TGAGGCTGCAGTAAG[-/C]CCATGACCGTTCCAC | 10138 |
rs35020261 | in-del | -/A | | | intron-variant | YAF2 | GRCh38.p7 | 12:42193319 | ATGAGACTCCCTCTC[-/A]AAAAAAAAAAAAAAA | 10138 |
rs35050500 | in-del | -/G | 0.462363 | 0.131916 | intron-variant | YAF2 | GRCh38.p7 | 12:42221473 | TACTTGGGAGGTTGA[-/G]GCTTGAGCCCAGGAG | 10138 |
rs35154804 | in-del | -/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42200754 | GAAATGAACTTTTCC[-/T]TTATATTTATGAGGT | 10138 |
rs35293070 | in-del | -/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42236228 | TACTCTAAACCAACT[-/C]CCAACCTTACACAGC | 10138 |
rs35426690 | in-del | -/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42178013 | ATAGGCTCCCTACCA[-/C]CCCCCCTAATTGTAA | 10138 |
rs35575791 | in-del | -/A | | | intron-variant | YAF2 | GRCh38.p7 | 12:42218950 | CTCCTGCCACCCTAC[-/A]AAAACTCACTAATAG | 10138 |
rs35606281 | in-del | -/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42202733 | AACCTCCGCCTCCCA[-/G]GTTCAAGCAATTCTC | 10138 |
rs35774429 | in-del | -/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42198792 | AGAAAAGACATCTGA[-/G]GGTGCCTTTATTGAA | 10138 |
rs35910821 | in-del | -/A | 0.00755907 | 0.0610114 | intron-variant | YAF2 | GRCh38.p7 | 12:42199792 | AAAGACTATTAGCTT[-/A]AAAAAAAAAGTATTA | 10138 |
rs35982219 | in-del | -/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42178031 | CCCTAATTGTAAACA[-/G]GGGACTTTTTCCTCT | 10138 |
rs36097397 | in-del | -/TG | 0.464096 | 0.129085 | intron-variant | YAF2 | GRCh38.p7 | 12:42161042 | ATGCAACCAAAAAAC[-/TG]TGACAGCCTAGAAGT | 10138 |
rs36107606 | in-del | -/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42201037 | ACACAGAAAGTACAA[-/G]GGAGTTTCTTAAGTT | 10138 |
rs55699566 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | YAF2 | GRCh38.p7 | 12:42199498 | ATTTACCACCAAAAA[A/G]TCCACACACCTTTCT | 10138 |
rs55910821 | in-del | -/A | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42196251 | AAAAAAAAAAAAAAA[-/A]GAGCGGGAGGACAGG | 10138 |
rs55985981 | in-del | -/AC/CA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42223332 | ACACACACACACACA[-/AC/CA]TATATATACACACAA | 10138 |
rs56126783 | snp | G/T | 0.0509478 | 0.151255 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42159005 | TAATAAACACAAATT[G/T]TAATTTTTCATTTAA | 10138 |
rs56355852 | in-del | -/A | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42206317 | AAAAAAAAAAAAAAA[-/A]GTGACGTCTGGCTGG | 10138 |
rs56394421 | in-del | -/ATA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42207475 | GATAAATTATTAATA[-/ATA]TTATACTAAATAATT | 10138 |
rs56687376 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | YAF2 | GRCh38.p7 | 12:42180221 | GATACAGCAAAAACC[A/G]ATTGGATGTCATTTC | 10138 |
rs56736670 | snp | A/C | 0.0352966 | 0.128072 | intron-variant | YAF2 | GRCh38.p7 | 12:42206577 | TAGCGCCACTGCACT[A/C]CAGCCTGGGAGACAG | 10138 |
rs56746293 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42182361 | CTTTACAGTTGGAAC[A/T]AAACACAAATGTGAA | 10138 |
rs57106203 | in-del | -/G | 0.0031463 | 0.0395379 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234192 | CCTCAAAAAAAAAAA[-/G]AGAAAAGAAAAGAAA | 10138 |
rs57549495 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | YAF2 | GRCh38.p7 | 12:42218020 | TTGAAAACAGATGTA[C/T]TCTTTAACTATGGCA | 10138 |
rs57579381 | snp | C/T | 0.313082 | 0.241911 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42237851 | CCGCCCCGCGGGCCC[C/T]CGGCGCGCCGCGCTC | 10138 |
rs57582332 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | YAF2 | GRCh38.p7 | 12:42178302 | CCACCCAGACCAATT[A/G]AATAAAAGACCTCCA | 10138 |
rs57632258 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | YAF2 | GRCh38.p7 | 12:42192673 | GAGTAGCCCAGAAAA[G/T]AGATGGTGGCTTAGG | 10138 |
rs57858521 | in-del | -/A | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234191 | CCTCAAAAAAAAAAA[-/A]GAGAAAAGAAAAGAA | 10138 |
rs58144362 | snp | G/T | 0.0452528 | 0.143452 | intron-variant | YAF2 | GRCh38.p7 | 12:42204146 | GGCAATAATTAAAAA[G/T]ATAATGAAAAGCATT | 10138 |
rs58369130 | snp | C/T | 0.0189856 | 0.0955633 | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42156744 | ACGTATATTCTGTAA[C/T]CTTGTCTTTTTATTC | 10138 |
rs58514363 | in-del | -/AA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42186211 | AAAAAAAAAAAAAAA[-/AA]GGCTGGGCTTGGTGG | 10138 |
rs58885852 | in-del | -/A | | | intron-variant | YAF2 | GRCh38.p7 | 12:42229436 | AAAAAAAAAAAAAAA[-/A]CATTTAAATATCTAC | 10138 |
rs59265941 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42223636 | AAAGTGCTGGGATTA[C/T]AGGTGTGAGCCACCT | 10138 |
rs59321905 | snp | A/G | | | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42209987 | ATTTTTCGTAGAGAC[A/G]GGGTTTCTCCATGTT | 10138 |
rs59450062 | in-del | -/AA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42206623 | AAAAAAAAAAAAAAA[-/AA]GTAACTGAAATTTTA | 10138 |
rs59476115 | in-del | -/AA | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42175770 | AAAAAAAAAAAAAAA[-/AA]TTAAAACAGGAATAC | 10138 |
rs59876649 | snp | C/T | 0.136847 | 0.222927 | intron-variant | YAF2 | GRCh38.p7 | 12:42188999 | GTAATGCTGAGACTA[C/T]ACCTACAACTGGGAG | 10138 |
rs60172480 | in-del | -/A | | | intron-variant | YAF2 | GRCh38.p7 | 12:42212035 | GCAAGATTTCATCTC[-/A]AAAAAAAAAAAGTCT | 10138 |
rs60207029 | snp | C/T | 0.171704 | 0.237423 | intron-variant | YAF2 | GRCh38.p7 | 12:42229243 | GTCATCACCAATCCC[C/T]AATCTCAAGTAATCA | 10138 |
rs60209608 | in-del | -/A | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234218 | AGAAAAGAAAAGAAA[-/A]GAAAAGAAAAGAAAG | 10138 |
rs60278477 | snp | A/G | 0.0799831 | 0.183287 | intron-variant | YAF2 | GRCh38.p7 | 12:42166137 | AGGCTGGTCTTGAAC[A/G]CCCAACCTCAGGTGA | 10138 |
rs60287587 | snp | A/G | 0.136506 | 0.222754 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239109 | TGTCCCCTCAACGCT[A/G]TCTGCTAACAAAAGA | 10138 |
rs61092335 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42176783 | CCTGGCCAATATGGC[A/G]AAACCCCGTCACCAC | 10138 |
rs61163063 | in-del | -/A | | | intron-variant | YAF2 | GRCh38.p7 | 12:42229422 | ATAAAAAAATAAATT[-/A]AAAAAAAAAAAAAAC | 10138 |
rs61303853 | in-del | -/AAAAAAAAAA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42175761 | AAAAAAAAAAAAAAA[-/AAAAAAAAAA]TTAAAACAGGAATAC | 10138 |
rs61366976 | snp | C/T | | | missense, nc-transcript-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42161665 | CCTTTTCACTTTTTT[C/T]TTTTTCTACTTTATC | 10138 |
rs61600160 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | YAF2 | GRCh38.p7 | 12:42206323 | AAAAAAAAAAGTGAC[A/G]TCTGGCTGGGCGCAG | 10138 |
rs61647009 | snp | C/T | 0.0759472 | 0.179459 | intron-variant | YAF2 | GRCh38.p7 | 12:42166207 | CATGAGCCATTGCGC[C/T]TGGCCTCAAATACAT | 10138 |
rs61940200 | snp | A/G | 0.0221141 | 0.102801 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157657 | GTTTTCACTTTGTCT[A/G]TTATCCACTATCATT | 10138 |
rs61940201 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42173062 | ACAGAGAGAGAGAGA[A/G]GGAGAGAGAGAAAGA | 10138 |
rs61940202 | snp | A/T | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42178629 | TTTTTATTTTTTAAA[A/T]TAAAAAAAAAATCTT | 10138 |
rs61940203 | snp | A/G | 0.303688 | 0.244167 | intron-variant | YAF2 | GRCh38.p7 | 12:42185135 | GTGGGCCAAGATCGC[A/G]CCACTGCACTCCAGC | 10138 |
rs61940204 | snp | A/G | 0.311728 | 0.242259 | intron-variant | YAF2 | GRCh38.p7 | 12:42185176 | GAGCCAGACTTTGTC[A/G]CAAACAAACAAACAA | 10138 |
rs61940205 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42185479 | TGAGTAAAATGCTAT[A/G]CAACAGCACTGCATG | 10138 |
rs61940206 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | YAF2 | GRCh38.p7 | 12:42191359 | CAACTTTTTCTAATA[A/G]TATGAATCCACTGAC | 10138 |
rs61940207 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | YAF2 | GRCh38.p7 | 12:42196183 | GGTGAGCCGAGATCA[C/T]GCCACTGCACTCCAG | 10138 |
rs61940225 | snp | A/G | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42213372 | GGCTTGTGAGAGAAA[A/G]GGTGGGAAAAAGAAC | 10138 |
rs61940226 | snp | G/T | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42213374 | CTTGTGAGAGAAAAG[G/T]TGGGAAAAAGAACAA | 10138 |
rs61940227 | snp | C/T | 0.330714 | 0.236612 | intron-variant | YAF2 | GRCh38.p7 | 12:42214604 | TTTCTGATTAAATGC[C/T]ACCCACTCAGAGAAG | 10138 |
rs61940228 | snp | A/C/T | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42215935 | AGCTCAAAAAATAAA[A/C/T]AAATAAATAAATAAA | 10138 |
rs61940229 | snp | A/G | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42217383 | ACACCCATAAATATA[A/G]GTGGGGAGACAATTA | 10138 |
rs61940230 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | YAF2 | GRCh38.p7 | 12:42223186 | ATAAAACTATCATAG[G/T]TGGGTGAAAGGTTTC | 10138 |
rs61940231 | snp | A/G | 0.362941 | 0.223034 | intron-variant | YAF2 | GRCh38.p7 | 12:42226889 | AGGCTCGAAGGCGCC[A/G]CGGGCTGGGGTCGGT | 10138 |
rs61940232 | snp | C/T | 0.331179 | 0.236453 | intron-variant | YAF2 | GRCh38.p7 | 12:42226959 | TGGTTGGCGCGGCTG[C/T]GCTGCGGCCCGGGGC | 10138 |
rs61940233 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42227006 | AGTCGCGGCGCTGAC[A/G]CCCGCGGGCCCCAGC | 10138 |
rs61940234 | snp | A/C | 0.5 | 0 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233233 | AACACCTATGAGAAA[A/C]CTAAAGGACTGTTAT | 10138 |
rs66732100 | in-del | -/A | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234215 | AAAAGAAAAGAAAAG[-/A]AAAGAAAAGAAAAGA | 10138 |
rs67295015 | in-del | -/TAAA | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42215975 | AAATAAATAAATAAA[-/TAAA]GCTACTGTACATTTA | 10138 |
rs67374165 | in-del | -/AGAAAAGAAAAGAAA | 0.410061 | 0.192043 | intron-variant, cds-indel | YAF2 | GRCh38.p7 | 12:42234193 | CTCAAAAAAAAAAAG[-/AGAAAAGAAAAGAAA]AGAAAAGAAAAGAAA | 10138 |
rs71084620 | in-del | -/TTTT | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42165793 | TTTTTTTTTTTTTTT[-/TTTT]AATGTAACTAACTCC | 10138 |
rs71084621 | in-del | -/A | 0.0142736 | 0.0832652 | intron-variant | YAF2 | GRCh38.p7 | 12:42175535 | TGTCAATTATACCTC[-/A]AAAAAAAAAAAGCTG | 10138 |
rs71084622 | in-del | -/A | | | intron-variant | YAF2 | GRCh38.p7 | 12:42179790 | CCTGTCTAAAAGGCA[-/A]AAAAAAAAAAAAAAA | 10138 |
rs71084623 | in-del | -/A | | | intron-variant | YAF2 | GRCh38.p7 | 12:42209564 | CCAGACTTTGTCTCA[-/A]AAAAAAAAAAAAAAA | 10138 |
rs71084625 | in-del | -/CACACA | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42218228 | ACACACACACACACA[-/CACACA]GATGATTATCGATCT | 10138 |
rs71084626 | in-del | -/G | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42228486 | AGGTGGGGGGGGGGG[-/G]TCAGCCCCCCCGCCT | 10138 |
rs71434389 | in-del | -/T | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42169879 | TCTCTCTCTCCTTTC[-/T]TTTTTTTTTAAGACA | 10138 |
rs71434390 | in-del | -/G | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42173056 | AGAGAGACAGAGAGA[-/G]AGAGAGGGAGAGAGA | 10138 |
rs71434392 | in-del | -/A | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42185157 | CACTCCAGCCTGGGC[-/A]ACAGAGCCAGACTTT | 10138 |
rs71434393 | in-del | -/AA | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42186189 | GCCAAACTCTGTCTC[-/AA]AAAAAAAAAAAAAAA | 10138 |
rs71434394 | in-del | -/T | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42191006 | GGGAATTTAAAAGTA[-/T]TTTTTTCTCTTTACA | 10138 |
rs71434396 | in-del | -/AC | 0.484066 | 0.0878235 | intron-variant | YAF2 | GRCh38.p7 | 12:42223331 | TTCTTTAAAATACAT[-/AC]ACACACACACACACA | 10138 |
rs71434397 | in-del | -/GGGG | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42228657 | GTCCGGGAGGGAGGT[-/GGGG]GGGGGGTCAGCCCCC | 10138 |
rs71441823 | multinucleotide-polymorphism | AAATTA/TAAATT | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42229416 | TTATCAATAAAAAAA[AAATTA/TAAATT]AAAAAAAAAAAAAAA | 10138 |
rs71452580 | snp | C/T | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42228674 | GGGGGGGGTCAGCCC[C/T]CCTGCCCGGCCAGCC | 10138 |
rs71453336 | snp | C/G | 0.0652144 | 0.168387 | intron-variant | YAF2 | GRCh38.p7 | 12:42175818 | GAGGATCTGTAGGCT[C/G]AAATTTTTTGAAAGT | 10138 |
rs71453337 | snp | C/T | 0.295854 | 0.245759 | intron-variant | YAF2 | GRCh38.p7 | 12:42193207 | GTAATCCCACCTACT[C/T]GGGAGGCTGAGGCAG | 10138 |
rs71453338 | snp | A/G | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42218256 | TCTCATCAAGGCTTA[A/G]GTATTTCATGGTATT | 10138 |
rs71453339 | snp | A/G | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42228588 | TCTGCCCGGCCAGCC[A/G]CCCCGTCAGGGAGGG | 10138 |
rs71453340 | snp | C/T | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42228592 | CCCGGCCAGCCGCCC[C/T]GTCAGGGAGGGAGGT | 10138 |
rs71453341 | snp | A/C | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42228596 | GCCAGCCGCCCCGTC[A/C]GGGAGGGAGGTGGGG | 10138 |
rs71453342 | snp | G/T | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42228613 | GGAGGGAGGTGGGGG[G/T]GTCAGCCCCCCGCCC | 10138 |
rs71453343 | snp | C/T | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42228628 | TGTCAGCCCCCCGCC[C/T]GGCCAGCCGCCCCGT | 10138 |
rs71453344 | snp | A/G | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42228646 | CCAGCCGCCCCGTCC[A/G]GGAGGGAGGTGGGGG | 10138 |
rs71453345 | snp | C/T | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42228698 | GCCAGCCGCCCCGTC[C/T]GGGAGGTGAGGGGCG | 10138 |
rs71453346 | snp | G/T | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42228788 | GTCCGGGAGGGAGGT[G/T]GGGGGGTCAGCCCCC | 10138 |
rs71883885 | in-del | -/AAC | | | intron-variant | YAF2 | GRCh38.p7 | 12:42218185 | TCAGGCTACTAGGAA[-/AAC]ACACACACACACACA | 10138 |
rs73114403 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | YAF2 | GRCh38.p7 | 12:42208585 | ACACTAGCCAATAAG[C/G]GTATTAACTGGGTGC | 10138 |
rs73114415 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | YAF2 | GRCh38.p7 | 12:42219509 | TCATTCAGAGAAGTG[G/T]TTGCTAAACAGAAAG | 10138 |
rs73114417 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | YAF2 | GRCh38.p7 | 12:42220421 | CTTACATAAAACATA[A/G]AAGATTTTCTAGTAA | 10138 |
rs73114420 | snp | A/T | 0.207253 | 0.246318 | intron-variant | YAF2 | GRCh38.p7 | 12:42221570 | TCTCTTTAAAAAAAA[A/T]TTTTTTTAAGTGACT | 10138 |
rs73114487 | snp | A/G | 0.136166 | 0.22258 | intron-variant | YAF2 | GRCh38.p7 | 12:42230391 | AAATGAAGCTAGGAA[A/G]GTAGTTTAGGGATAG | 10138 |
rs73114491 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233345 | AACCAATAATTCTAT[C/T]ATTTTCATTTCTAAA | 10138 |
rs73114498 | snp | A/T | 0.0814217 | 0.184611 | intron-variant, synonymous-codon, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42235799 | CCCATGTGGGCCTCA[A/T]GCCTCTTTTAAACTA | 10138 |
rs73127418 | snp | A/T | 0.135484 | 0.22223 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157298 | TCTTGTGAGAATTCA[A/T]CCATTCCTGCAAGAG | 10138 |
rs73127421 | snp | C/T | 0.132751 | 0.2208 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42158657 | CTCCATGCTACACCG[C/T]GTTCCCGTCTATGTA | 10138 |
rs73127428 | snp | A/T | 0.135484 | 0.22223 | intron-variant | YAF2 | GRCh38.p7 | 12:42164595 | TAAAAAGAGGCAGCA[A/T]AACTCAAATTTCAAA | 10138 |
rs73127430 | snp | C/T | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42164790 | ACCACCTGTTTACAA[C/T]CAAGCGTGGTGGCTC | 10138 |
rs73127435 | snp | A/G | 0.136166 | 0.22258 | intron-variant | YAF2 | GRCh38.p7 | 12:42165349 | AGAGAACAATGAAAC[A/G]ACTTCATTAAGCATT | 10138 |
rs73127445 | snp | A/G | 0.0759472 | 0.179459 | intron-variant | YAF2 | GRCh38.p7 | 12:42173905 | TGTCCACAGCCTTCC[A/G]TCTGTACCGACATAG | 10138 |
rs73127453 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | YAF2 | GRCh38.p7 | 12:42178370 | TGGGCTGCTCCTATT[A/G]TGCAGTCAATGGCCT | 10138 |
rs73131138 | snp | C/T | 0.168135 | 0.236216 | intron-variant | YAF2 | GRCh38.p7 | 12:42185921 | AAAGTCAGGCTGGGC[C/T]GGGCACAGTGGCTCA | 10138 |
rs73131166 | snp | A/G | 0.0770498 | 0.180522 | intron-variant | YAF2 | GRCh38.p7 | 12:42207112 | AATAAAAGCACTCTC[A/G]ATATAACGACCATAT | 10138 |
rs73281838 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | YAF2 | GRCh38.p7 | 12:42172727 | TAACAGCCCCAAAGC[A/G]GAAGCAACCCAAATG | 10138 |
rs73281848 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | YAF2 | GRCh38.p7 | 12:42180581 | TGAGATATAAATGTC[A/G]GTAAGTAGCTAAGTT | 10138 |
rs73281851 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | YAF2 | GRCh38.p7 | 12:42185722 | AAATTAAGGTATATA[C/T]ATTGTTGTTTTTGGA | 10138 |
rs73281857 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | YAF2 | GRCh38.p7 | 12:42192687 | AGAGATGGTGGCTTA[C/G]GGTAGCTGACAAATG | 10138 |
rs73281860 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | YAF2 | GRCh38.p7 | 12:42196986 | TCAAGTAACCACCAC[C/T]TGAGAAGGCAGTGTC | 10138 |
rs73281868 | snp | A/T | 0.0429648 | 0.14013 | intron-variant | YAF2 | GRCh38.p7 | 12:42200405 | TCACCTTCTTATCCC[A/T]AGCACCTAGTGCTTA | 10138 |
rs73281880 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | YAF2 | GRCh38.p7 | 12:42204279 | ACACGAAGTATCACA[C/T]GACCCAGCAATTTCA | 10138 |
rs73281886 | snp | C/G | 0.0441095 | 0.141807 | intron-variant | YAF2 | GRCh38.p7 | 12:42216091 | TAATCTAAAGTCATT[C/G]TTAGAGGCATAGACT | 10138 |
rs73281890 | snp | A/C | 0.0244538 | 0.107838 | intron-variant | YAF2 | GRCh38.p7 | 12:42223300 | AATTATATAACTATC[A/C]TCTTAAAAACAGCAG | 10138 |
rs73281894 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | YAF2 | GRCh38.p7 | 12:42226173 | TCTTAATACGCTGTA[C/T]ACTTTCACAGCTTCA | 10138 |
rs73281897 | snp | G/T | 0.0433465 | 0.140692 | intron-variant | YAF2 | GRCh38.p7 | 12:42226603 | TGGGAGGTTGAGGCT[G/T]CAGTAAGCTATATCC | 10138 |
rs73283703 | snp | A/G | 0.046775 | 0.145601 | intron-variant | YAF2 | GRCh38.p7 | 12:42230315 | GAAAGAGAAAGAAAA[A/G]GTACCATATGATAAA | 10138 |
rs73283707 | snp | A/C | 0.0444908 | 0.142359 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232672 | TCCTACACCAAAAGT[A/C]TAGAAGAATCAGTGC | 10138 |
rs74078178 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | YAF2 | GRCh38.p7 | 12:42163069 | GCTTAGCCCTACCCC[A/G]CAGGATTTCTGATTC | 10138 |
rs74078179 | snp | G/T | 0.0509478 | 0.151255 | intron-variant | YAF2 | GRCh38.p7 | 12:42163138 | AACTAGTTTCCAAGT[G/T]ATGCTGATGTCTCTG | 10138 |
rs74078180 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | YAF2 | GRCh38.p7 | 12:42163533 | GTGGTTCTTTTTTTC[C/T]GTTCTTGAGTAGTTG | 10138 |
rs74078190 | snp | A/G | 0.477004 | 0.104734 | intron-variant | YAF2 | GRCh38.p7 | 12:42174100 | TTCATACCTCAAAAA[A/G]AAAAAAAAAAAAAAA | 10138 |
rs74078194 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | YAF2 | GRCh38.p7 | 12:42178687 | AACTACTTATATTTC[C/T]TTTTAACCCTCAAAG | 10138 |
rs74078197 | snp | A/T | 0.0509478 | 0.151255 | intron-variant | YAF2 | GRCh38.p7 | 12:42181379 | GGTTTTAAGAGTCAT[A/T]GTCAGGCAGTAGTAT | 10138 |
rs74081009 | snp | A/T | 0.0509478 | 0.151255 | intron-variant | YAF2 | GRCh38.p7 | 12:42194893 | GCTGTGTAACTCTCT[A/T]ATAGTTCACATGTAA | 10138 |
rs74081014 | snp | C/T | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42218814 | TATGTAGCTCTGAGC[C/T]TTACTAATCTCGGTC | 10138 |
rs74334107 | snp | A/T | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42188405 | TTTTTTTTTTTTTAG[A/T]GACAGAGTCTTACTC | 10138 |
rs74341899 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | YAF2 | GRCh38.p7 | 12:42170921 | TTTCCCCTAATATCC[A/G]CTCTAAATGTTGAAT | 10138 |
rs74343037 | snp | A/T | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42192798 | AGTTACATAGTTTAC[A/T]TCTAGTTCTTTGCAA | 10138 |
rs74354786 | snp | C/T | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42237022 | GATATAAAGGTACTT[C/T]CAGTAAAAATCTGTT | 10138 |
rs74405182 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | YAF2 | GRCh38.p7 | 12:42220548 | GGAACAAAAGACAAA[G/T]AGCAAAAATGGATGG | 10138 |
rs74428333 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42193889 | GGCAGAGGAAGAAGA[C/G]AGTGATATTTATGGA | 10138 |
rs74429169 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | YAF2 | GRCh38.p7 | 12:42182735 | TATATTGAATTTTCC[A/G]TCTTAATATAAACTG | 10138 |
rs74431742 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42218170 | TATGTGACAGTCTAC[A/G]TCAGGCTACTAGGAA | 10138 |
rs74591832 | snp | A/T | 0.136506 | 0.222754 | intron-variant | YAF2 | GRCh38.p7 | 12:42178277 | TTTTAAAATTACTAT[A/T]CTTGGGCCCCCACCC | 10138 |
rs74735383 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | YAF2 | GRCh38.p7 | 12:42220722 | AAGTAAAGTATGTTG[C/T]GCAAAGGAACCCTGA | 10138 |
rs74920861 | in-del | -/GGA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42196226 | AGCAAGAATCCATCT[-/GGA]AAAAAAAAAAAAAAA | 10138 |
rs74936057 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | YAF2 | GRCh38.p7 | 12:42216975 | GTTCCACAGATCTCT[C/T]CTAAACACATCTATA | 10138 |
rs75043397 | in-del | -/TT | | | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42157073 | TCCACTTTTTTTTTT[-/TT]GCTATAACAGAATAC | 10138 |
rs75075777 | snp | A/T | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42172505 | AACATGAGACCTGAA[A/T]TTTTTTTAAGCGACT | 10138 |
rs75085410 | snp | A/C | 0.334412 | 0.235318 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238552 | TGCCCCCTTGGTACC[A/C]CCGGCTGCCGGGGAC | 10138 |
rs75092573 | in-del | -/AAGAAAAGAAAA | | | intron-variant, cds-indel | YAF2 | GRCh38.p7 | 12:42234197 | AAAAAAAAAAGAGAA[-/AAGAAAAGAAAA]GAAAAGAAAAGAAAA | 10138 |
rs75104182 | snp | A/T | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42188700 | CAGAATTTTTTTTTT[A/T]AATTTAAAAAATGTT | 10138 |
rs75113098 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42229474 | CAGGTATTTTATTAG[C/T]TTCTGGGAATACCAA | 10138 |
rs75221287 | snp | A/C | 0.0376037 | 0.131863 | intron-variant | YAF2 | GRCh38.p7 | 12:42218530 | TGTATGTGTCTTTTA[A/C]AAAATGTATTATTTT | 10138 |
rs75262064 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42218989 | TTTGAAATGTGAGGG[A/T]AGGTAATCCAGTCAC | 10138 |
rs75277041 | in-del | -/TTT | | | intron-variant | YAF2 | GRCh38.p7 | 12:42222949 | ATTCTTTTTTTTTTT[-/TTT]GTTACCATTGGTAGT | 10138 |
rs75286201 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | YAF2 | GRCh38.p7 | 12:42184726 | AAAGGCTTCGCCATT[A/C]TAGATGTCATTAAGA | 10138 |
rs75308746 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | YAF2 | GRCh38.p7 | 12:42220695 | GTTGACTGTCCCTAG[C/T]ATGTTCTATAAAAGT | 10138 |
rs75337280 | snp | C/T | 0.0248432 | 0.108648 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233202 | ATGTGAAATCTTTTT[C/T]ATAGCTCTCTAAAAT | 10138 |
rs75405117 | snp | C/G | 0.0248432 | 0.108648 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42158710 | TATGTAGAAATATGA[C/G]TATGCTCCATTCAGG | 10138 |
rs75457115 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42180736 | GGTGGATCGCTTGAG[A/G]CCAGGAGTTTGAGAC | 10138 |
rs75476797 | snp | A/G | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42206314 | AAAAAAAAAAAAAAA[A/G]AAAGTGACGTCTGGC | 10138 |
rs75499229 | snp | A/C | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42165064 | TGTCTTCTGGAACAA[A/C]AAAAAAAAAAAAAAA | 10138 |
rs75774725 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | YAF2 | GRCh38.p7 | 12:42187541 | AAGAATACTAAAGAT[G/T]GAGATACAATGGCAT | 10138 |
rs75777377 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | YAF2 | GRCh38.p7 | 12:42199311 | CAATAGTTTAAATCC[A/G]TCAAACATAATAATA | 10138 |
rs75785413 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | YAF2 | GRCh38.p7 | 12:42206105 | TCTGTGCTTGTCCGG[A/T]GGAGTACTCATTTCT | 10138 |
rs75803618 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | YAF2 | GRCh38.p7 | 12:42197854 | AGAAGTTATAAACTC[A/T]ATTACTGAAAATAAT | 10138 |
rs75846646 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | YAF2 | GRCh38.p7 | 12:42190726 | TGCCAGTCTGCAGTA[C/T]CTTTAGACCTTTGAC | 10138 |
rs75877968 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42169247 | TTTAACATTCTCCTG[C/T]ACCATAGCTACAAAG | 10138 |
rs75904539 | snp | A/C | 0.00272479 | 0.0368099 | intron-variant | YAF2 | GRCh38.p7 | 12:42205892 | CTTTTGTTGTGATTT[A/C]GTTCTAATTATTTTG | 10138 |
rs75908309 | snp | G/T | 0.0352966 | 0.128072 | intron-variant | YAF2 | GRCh38.p7 | 12:42182244 | ACGAGGAAGCAGAAG[G/T]CATGAAATTCTGTTA | 10138 |
rs75994497 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | YAF2 | GRCh38.p7 | 12:42220074 | ACCAAGATGAGGTGA[A/G]AATGGTTATGAGAAG | 10138 |
rs76029084 | snp | C/T | 0.0248432 | 0.108648 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42161369 | CAAAACAAAACAAAT[C/T]CAGACACAAATGTCT | 10138 |
rs76044215 | in-del | -/CAAAAAAAAAA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42175740 | AGCAAGACTCTGTCT[-/CAAAAAAAAAA]AAAAAAAAAAAAAAA | 10138 |
rs76103158 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | YAF2 | GRCh38.p7 | 12:42187348 | AAATTTTTGTAGAGA[C/T]GGGGTTCTGTTATGT | 10138 |
rs76212513 | snp | C/G | 0.0352966 | 0.128072 | intron-variant | YAF2 | GRCh38.p7 | 12:42177524 | AGGCCACCAATCCTA[C/G]TGGATTAGGACTCCA | 10138 |
rs76213486 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | YAF2 | GRCh38.p7 | 12:42187615 | AATCCTACTCTGATA[C/T]TTACGTAAAAATCCT | 10138 |
rs76235749 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | YAF2 | GRCh38.p7 | 12:42180390 | GGTCCAACTGCCAGC[A/G]AAGAACTGAGGTCAA | 10138 |
rs76239453 | snp | A/C | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42229434 | ATTAAAAAAAAAAAA[A/C]AACATTTAAATATCT | 10138 |
rs76276256 | snp | A/T | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42178640 | TAAAATAAAAAAAAA[A/T]TCTTCTGTCCAATGT | 10138 |
rs76363194 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | YAF2 | GRCh38.p7 | 12:42216212 | ACCTCCTTTATTTAG[C/T]CTATAAATATAAACC | 10138 |
rs76395159 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | YAF2 | GRCh38.p7 | 12:42175235 | AAGAGGAGTTATGCC[A/G]AGTGAAAGAGATTGG | 10138 |
rs76437465 | snp | C/T | 0.0252325 | 0.109451 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42231674 | GTTTGCTGAGTTATG[C/T]GTAGCTTCCAAATGC | 10138 |
rs76440084 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | YAF2 | GRCh38.p7 | 12:42186851 | AAGAAACACCCATCA[G/T]TAGGAAATTATCCTT | 10138 |
rs76459700 | snp | A/T | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42167905 | TACAGTCCAGGACAG[A/T]CAAGTCATCGTCTGG | 10138 |
rs76646834 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157551 | CATTAATGCAGAGGC[C/T]ACATTCTTTCAGTCT | 10138 |
rs76720834 | snp | A/T | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42165798 | TTTTTTTTTTTTTTA[A/T]TGTAACTAACTCCTC | 10138 |
rs76950466 | snp | C/T | 0.021333 | 0.101051 | intron-variant | YAF2 | GRCh38.p7 | 12:42164050 | ATGGTTTTGACAGTA[C/T]ACTTTTAGTAATGCC | 10138 |
rs76958210 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | YAF2 | GRCh38.p7 | 12:42223249 | ATAGCGCCAGCATAC[C/T]ATGTAGGAAGTTTCA | 10138 |
rs77009681 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42191153 | GTTTTTAAAGTCTAC[C/T]ATTGCTGTTAATGTT | 10138 |
rs77010814 | snp | A/G | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42196232 | AATCCATCTGGAAAA[A/G]AAAAAAAAAAAAAAA | 10138 |
rs77038056 | snp | A/C | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42167984 | AAGCCAAATAAAATA[A/C]TGAATGTTAAAAATG | 10138 |
rs77054045 | snp | A/C | 0.0524604 | 0.153226 | intron-variant | YAF2 | GRCh38.p7 | 12:42203740 | ATGTCTGTGTTCATA[A/C]GTAAGACTGAATGTA | 10138 |
rs77108439 | snp | A/T | 0.0111619 | 0.0738673 | intron-variant, nc-transcript-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42210385 | TCCTATTGGGTCTTT[A/T]CCCTCACAGATCCAC | 10138 |
rs77135603 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | YAF2 | GRCh38.p7 | 12:42182929 | TTTATTACTTTTTAC[A/C]AATTGAAGGTTTGTG | 10138 |
rs77155289 | snp | C/G | 0.0352966 | 0.128072 | intron-variant | YAF2 | GRCh38.p7 | 12:42170289 | GTAACAAGCTCAGAG[C/G]CTGATAGGCATTCAA | 10138 |
rs77270708 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | YAF2 | GRCh38.p7 | 12:42164120 | TGCCTAGTTAATAAA[C/T]GACTACTGTCTAGCC | 10138 |
rs77300573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42186918 | TATCTGAGCAAGCCA[C/T]TGCTTGCCACCAATT | 10138 |
rs77317721 | snp | C/T | 0.021333 | 0.101051 | intron-variant | YAF2 | GRCh38.p7 | 12:42219510 | CATTCAGAGAAGTGT[C/T]TGCTAAACAGAAAGG | 10138 |
rs77320363 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | YAF2 | GRCh38.p7 | 12:42218120 | TACCAGAGTACTTTC[C/T]AGACGTTAGAACTTG | 10138 |
rs77330786 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42200946 | AAATGAAGATAATGA[C/T]AGTACCTCTTTCTGA | 10138 |
rs77343264 | snp | A/G | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42193628 | GTCCCAGCTACTCGG[A/G]GACTGGGGTGGAAGG | 10138 |
rs77447387 | snp | C/G | 0.0509478 | 0.151255 | intron-variant | YAF2 | GRCh38.p7 | 12:42187553 | GATTGAGATACAATG[C/G]CATAACGTTTAAGAG | 10138 |
rs77484967 | snp | A/G | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42193609 | TGGGGTGGAAGGATC[A/G]CTTGAGCCCAGGAGG | 10138 |
rs77544400 | snp | A/C | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42196220 | CGACAGAGCAAGAAT[A/C]CATCTGGAAAAAAAA | 10138 |
rs77553803 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | YAF2 | GRCh38.p7 | 12:42177775 | CAAATGTCAGAGAAG[C/T]CTTCCTTTTTACTTT | 10138 |
rs77573743 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | YAF2 | GRCh38.p7 | 12:42171495 | CAACGTGGTATGACC[A/C]CATCTCTTTAAATTA | 10138 |
rs77600253 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42200087 | TTACTAAGCAAAAGG[C/T]ATTACACTAAATTTT | 10138 |
rs77626513 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | YAF2 | GRCh38.p7 | 12:42190261 | AGGAAGGATGATCTC[C/T]TGAGCCTGGGAAGCA | 10138 |
rs77645443 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | YAF2 | GRCh38.p7 | 12:42177825 | TGAATGCCAGACCAT[A/G]ATTGTAGGAGAAGTC | 10138 |
rs77657503 | snp | A/T | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42197747 | ATAATCAGACTCCAA[A/T]TAATCTTACCTTACA | 10138 |
rs77682585 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42218660 | TTATGGCATTCGGGA[A/C]CCTATCTTTTGGGAT | 10138 |
rs77768607 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | YAF2 | GRCh38.p7 | 12:42187937 | GCTCTTATGTCATGG[C/G]GACACTCAAGCAGCC | 10138 |
rs77781527 | in-del | -/CAAAAAATAA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42215924 | AGCGAGATTCCAGCT[-/CAAAAAATAA]ATAAATAAATAAATA | 10138 |
rs77803042 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42203453 | GTATTGATAGAGATA[C/T]ATCTGTCTTACCCTT | 10138 |
rs77806887 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42163896 | TCCAGGTATCTTAAG[G/T]TTTGTGATCCCTTTT | 10138 |
rs77874700 | snp | C/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233764 | GAAATCCTCCTGTCT[C/T]AGCCTCCCAAGGTGC | 10138 |
rs77883571 | snp | C/G | 0.00953873 | 0.0683987 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42158787 | AAATACATCCTGAAA[C/G]TTATTTGATCATAAG | 10138 |
rs77890158 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42183114 | CATTGTTTTGAGGAG[C/T]CAAGGCCCACACCTG | 10138 |
rs77902404 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157200 | CCTCATGCTGCTTCA[A/G]CTCATGGTGGAAAGC | 10138 |
rs78021697 | snp | C/T | 0.0622301 | 0.165053 | intron-variant | YAF2 | GRCh38.p7 | 12:42216815 | TTACCTTCCCCCAAA[C/T]CTGTCTTCCTATTTG | 10138 |
rs78062157 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42200684 | TTGCAATGACATCCA[C/G]AGGCAACCACTATCA | 10138 |
rs78226327 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | YAF2 | GRCh38.p7 | 12:42172858 | ACATGGATGAGCCTA[C/T]GGCATTATGCTAAGT | 10138 |
rs78242399 | snp | A/G | 0.0376037 | 0.131863 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42240186 | ATCCACCTTAAATAG[A/G]AAATATTGTAAATTG | 10138 |
rs78286342 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | YAF2 | GRCh38.p7 | 12:42216266 | TGAGGACAATCACTA[C/T]GCAAAAGTATTATCT | 10138 |
rs78445494 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | YAF2 | GRCh38.p7 | 12:42183442 | ATAAAGAAAAGCTGT[C/G]GAAGGAAATTTAGAA | 10138 |
rs78446256 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160282 | ATAGTAGAGAATTCA[A/G]GAATTATGTGTTAGA | 10138 |
rs78469271 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42210064 | TGGCCTCCAAAAGTA[C/T]TGGGATTACAAGTGT | 10138 |
rs78514668 | snp | A/C | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42193318 | AATGAGACTCCCTCT[A/C]AAAAAAAAAAAAAAA | 10138 |
rs78516026 | snp | A/T | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42165793 | TTTTTTTTTTTTTTT[A/T]TTTAATGTAACTAAC | 10138 |
rs78539383 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42175234 | CAAGAGGAGTTATGC[C/T]GAGTGAAAGAGATTG | 10138 |
rs78585388 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | YAF2 | GRCh38.p7 | 12:42212105 | AAAGTATGCCAGTCA[C/T]TGAAAAATATTAATA | 10138 |
rs78588712 | snp | G/T | 0.0429648 | 0.14013 | intron-variant | YAF2 | GRCh38.p7 | 12:42196426 | AGTACATGAAACGAT[G/T]TGCAAGCCATGTTAA | 10138 |
rs78689030 | snp | C/G | 0.0165278 | 0.0893908 | intron-variant | YAF2 | GRCh38.p7 | 12:42171638 | CTGGGTATATAACTC[C/G]TGATCATTTTCTCAT | 10138 |
rs78729667 | in-del | -/AA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42165078 | AAAAAAAAAAAAAAA[-/AA]GAAAAGAAACTACTT | 10138 |
rs78760512 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | YAF2 | GRCh38.p7 | 12:42195019 | ATTAGTTAAAATATT[A/G]TACCAACAGGTAGTT | 10138 |
rs78765945 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | YAF2 | GRCh38.p7 | 12:42204836 | CAAAACACATGTTGT[A/G]TAATTCCATTTTATG | 10138 |
rs78784702 | snp | C/G | 0.0607341 | 0.163335 | intron-variant | YAF2 | GRCh38.p7 | 12:42164859 | CAGATCATTTGAGTC[C/G]AGGAGTTCGAGGCCA | 10138 |
rs78941210 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42197001 | CTGAGAAGGCAGTGT[C/G]TGTTTTGTTCACTTC | 10138 |
rs78942159 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42182247 | AGGAAGCAGAAGGCA[C/T]GAAATTCTGTTAACA | 10138 |
rs78948812 | in-del | -/CA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42171799 | TCTCTACAGAAAATA[-/CA]AAAAAAAAAAAAAAT | 10138 |
rs78998371 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42166894 | TTTTGTACTTTCTGG[A/G]AAGATGATAAAACAC | 10138 |
rs79007195 | snp | A/G | 0.0248432 | 0.108648 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42230779 | AATATACAGATGCCA[A/G]GTTTGGGGAGGCAGA | 10138 |
rs79029651 | snp | C/T | 0.0252325 | 0.109451 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232412 | CTACACTTTGAAAAC[C/T]ACTCTGATATCCAGA | 10138 |
rs79030781 | snp | A/T | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42165794 | TTTTTTTTTTTTTTT[A/T]TTAATGTAACTAACT | 10138 |
rs79076196 | snp | A/G | 0.136166 | 0.22258 | intron-variant | YAF2 | GRCh38.p7 | 12:42236612 | TTTTAGAAATCTAAC[A/G]TCTACTGAATATTTG | 10138 |
rs79098845 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | YAF2 | GRCh38.p7 | 12:42188198 | AGTGGTTTCTGGCAC[A/G]GGAAAGGGGAATACA | 10138 |
rs79149298 | snp | C/T | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42211427 | GCGAGACTCTGTCTC[C/T]AAAAAAAAAAAAAAA | 10138 |
rs79260869 | snp | A/G | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42219952 | TATTATAATTGAAAA[A/G]CAAAGTTCCCTGGTA | 10138 |
rs79333562 | snp | A/G | 0.0532157 | 0.154195 | intron-variant | YAF2 | GRCh38.p7 | 12:42168001 | GAATGTTAAAAATGT[A/G]TATACTGTAAGTTAT | 10138 |
rs79360946 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | YAF2 | GRCh38.p7 | 12:42163916 | TGATCCCTTTTCTAT[C/T]TGATGAGAAAAATCA | 10138 |
rs79366410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42197380 | ATAGAATGTGTGATC[A/G]CAGTGGATGGGAGAA | 10138 |
rs79382783 | snp | C/T | 0.00770623 | 0.0615933 | intron-variant, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42212427 | TACCCTTTACCATCA[C/T]GCTTCTAAATAATCA | 10138 |
rs79389431 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42178654 | AATCTTCTGTCCAAT[C/G]TGTCAGCACCACTTT | 10138 |
rs79397427 | snp | A/C | | | synonymous-codon, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160808 | AGCACTACTCCGATC[A/C]ACATTTTTCAATCTT | 10138 |
rs79463144 | snp | C/T | 0.0271762 | 0.113356 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42158489 | ATTAAGAATTTTACA[C/T]GGATTGACTTAATCC | 10138 |
rs79487077 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | YAF2 | GRCh38.p7 | 12:42215642 | AGCTACCATACAGTG[G/T]CAGGGCATGGTGGCT | 10138 |
rs79726363 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | YAF2 | GRCh38.p7 | 12:42180195 | CCTAGTGAGGTGCTT[C/T]TAATAAATAGGATAC | 10138 |
rs79785124 | snp | A/G | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42175544 | TACCTCAAAAAAAAA[A/G]AAGCTGTCTAAAATT | 10138 |
rs79961212 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42237302 | ATTTTTATACCCAGA[A/G]TGGGGAGAGGGGCAT | 10138 |
rs79965845 | snp | A/T | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42178896 | AGCTTTAAAAAAAAA[A/T]TACCCCTTTAGCCAG | 10138 |
rs79972163 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42222937 | TATTGCTGCCAAATT[C/T]TTTTTTTTTTTTTTG | 10138 |
rs80014650 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | YAF2 | GRCh38.p7 | 12:42202130 | CTAGAAAACCAATTC[A/G]ACAGTCTACTTTTTC | 10138 |
rs80021708 | snp | A/C/G | 0.013901 | 0.0823931 | intron-variant | YAF2 | GRCh38.p7 | 12:42180457 | CCTGTCGGGACCCTT[A/C/G]AGAGAGCTGCAGCCC | 10138 |
rs80029282 | snp | C/G | 0.0696718 | 0.173152 | intron-variant | YAF2 | GRCh38.p7 | 12:42218901 | AGGGAAGGAGGGAGA[C/G]AGAAAGGGCTTTCAA | 10138 |
rs80039797 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42200377 | CTCCTTAAAGAGAGA[A/G]GCTGAAAACTATTCA | 10138 |
rs80078451 | snp | A/C/T | 0.0509478 | 0.151255 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234805 | CTAGCCTAGGCAACA[A/C/T]AGAGATCCCCCATCT | 10138 |
rs80090787 | snp | A/T | 0.5 | 0 | intron-variant, utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42235771 | CTGGTAAAAAAAAAA[A/T]ATGTCAGGGGCCCCC | 10138 |
rs80129798 | snp | A/G | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42196917 | CTGACTGGGACCTCA[A/G]GGCAGTGAAGATTTA | 10138 |
rs80137606 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42203066 | GAAGGTCATTTTCCA[A/C]AAAAAAAAAAAAAAA | 10138 |
rs80233023 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | YAF2 | GRCh38.p7 | 12:42189847 | AATTAGTCTAAGACA[A/G]GCACATTTTGTTAAT | 10138 |
rs80236766 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232328 | ATCTTCAAATTATTA[C/T]AAAAACAGTGTGAAC | 10138 |
rs80245881 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | YAF2 | GRCh38.p7 | 12:42176548 | AGCAGTATTTATTCC[A/G]TTTTTCCTCTCATAC | 10138 |
rs80251304 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | YAF2 | GRCh38.p7 | 12:42185584 | TACAGCCACCCCAAC[C/T]TTCAACAATCACCAA | 10138 |
rs80285467 | snp | G/T | 0.245346 | 0.249957 | intron-variant | YAF2 | GRCh38.p7 | 12:42170991 | TCAGGAATTGTTTAG[G/T]TTTTTTTTGTTTTTG | 10138 |
rs80301988 | in-del | -/AA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42175545 | ACCTCAAAAAAAAAA[-/AA]GCTGTCTAAAATTTT | 10138 |
rs80307050 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | YAF2 | GRCh38.p7 | 12:42178382 | ATTGTGCAGTCAATG[A/G]CCTATAAAACAAGAT | 10138 |
rs80308513 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | YAF2 | GRCh38.p7 | 12:42170718 | GGGCATGGTGGCAAG[C/T]ACCTTTAGTCCCAGC | 10138 |
rs80324953 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | YAF2 | GRCh38.p7 | 12:42208679 | ACTGAAGAACTGAAG[A/G]TAACAAATATACTAG | 10138 |
rs80327846 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42203490 | AATGAGAATGTTTCC[A/G]AAGTTTCACTATTAA | 10138 |
rs111290001 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | YAF2 | GRCh38.p7 | 12:42204767 | GTGTACTGACATATG[C/G]TACAATGCGGATAAA | 10138 |
rs111320230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42218440 | TTGCAAAAATGTTAT[C/T]GCCTATTTTATTGTG | 10138 |
rs111325216 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42161237 | CTAATAAGGGTATCA[C/T]GATTGTTATGACTGA | 10138 |
rs111382074 | snp | C/T | 0.5 | 0 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42161602 | TGTCATAAAACACTC[C/T]TCACATTTACCTGGT | 10138 |
rs111628876 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | YAF2 | GRCh38.p7 | 12:42219115 | TAAGAGAAATCCTAA[C/T]AAAATATATAATGGC | 10138 |
rs111748211 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | YAF2 | GRCh38.p7 | 12:42193080 | GCACTTTGGGTGGCC[A/G]AGGGGGGGCAGATCA | 10138 |
rs111793912 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | YAF2 | GRCh38.p7 | 12:42192237 | TTTTGGCTGAGCATC[A/G]TGGCACATGCCTGTA | 10138 |
rs111824538 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42227816 | GGTCAGCCCCCCGCC[C/T]GGCCAGCCGTGCCGT | 10138 |
rs111851937 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42160937 | AATACATGTATTTAA[A/G]GCAATTTATGTGTAA | 10138 |
rs111886233 | snp | A/G | 0.0248432 | 0.108648 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42161546 | TGTGTATATTAGTAT[A/G]TCAAGGTTAAAAAAA | 10138 |
rs111943700 | snp | C/T | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42169084 | AAAATGTCTGCTATT[C/T]TCTCAGTTGTGTCCT | 10138 |
rs112005724 | snp | C/T | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42220939 | CTTACTGGTATTTCT[C/T]CTGAGAAACACTATG | 10138 |
rs112167299 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | YAF2 | GRCh38.p7 | 12:42212752 | TTCTTACTTAAATTT[A/G]AGATACAAATTGCCT | 10138 |
rs112374101 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | YAF2 | GRCh38.p7 | 12:42222055 | AGAATGAAGTACATA[C/T]AGAATCTTTTAAAAC | 10138 |
rs112421904 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | YAF2 | GRCh38.p7 | 12:42194462 | CAGTCTGGCCAACAC[A/G]GTGAAAACCCGTCTC | 10138 |
rs112631828 | snp | C/G | 0.0441095 | 0.141807 | intron-variant | YAF2 | GRCh38.p7 | 12:42215921 | CAGAGCGAGATTCCA[C/G]CTCAAAAAATAAATA | 10138 |
rs112634970 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | YAF2 | GRCh38.p7 | 12:42197600 | TTGCATGTGAGATTC[C/T]GCTGGAATAGAGGTG | 10138 |
rs112702157 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42228934 | AGCTCATTGAGAACG[A/G]GCCATGATGACAATG | 10138 |
rs112834663 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | YAF2 | GRCh38.p7 | 12:42164846 | AGGCCAAGGCAGGCA[G/T]ATCATTTGAGTCCAG | 10138 |
rs112891322 | snp | A/G | 0.465996 | 0.12588 | intron-variant | YAF2 | GRCh38.p7 | 12:42168305 | TGCCTCAGCCTCTCT[A/G]GTAGCTGGGATTACA | 10138 |
rs112892652 | snp | A/C | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42194963 | TATAGACATACATCA[A/C]ACATGTATACATGGT | 10138 |
rs112950367 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | YAF2 | GRCh38.p7 | 12:42218029 | GATGTACTCTTTAAC[C/T]ATGGCAAACAGTAAA | 10138 |
rs113062566 | snp | G/T | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42225094 | TGAGATACTATCTCA[G/T]TGTGGTTTGATGTGC | 10138 |
rs113207347 | snp | C/T | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42213303 | GTCTGCTGACAACCA[C/T]ATGAGTGAGCTTGCA | 10138 |
rs113211489 | snp | C/T | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42223355 | ACACACACACACACA[C/T]ATATATATACACACA | 10138 |
rs113303787 | snp | C/G | 0.0689305 | 0.172377 | intron-variant | YAF2 | GRCh38.p7 | 12:42224643 | TTTGGTTTTCTGATC[C/G]TGTGTTAGTGTGCTG | 10138 |
rs113341539 | snp | A/G | 0.0170251 | 0.090679 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42231278 | AAACAAAGATATTTT[A/G]TATGAAGAGTGGCAT | 10138 |
rs113345214 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42172318 | GTCGTACAAAATTAT[A/G]AATTATTATAATTTG | 10138 |
rs113426090 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | YAF2 | GRCh38.p7 | 12:42186121 | GCTTGAACCCAGGAG[A/G]CAGAGGTTGCAGTGG | 10138 |
rs113444083 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | YAF2 | GRCh38.p7 | 12:42230212 | CAGTGAGCCAAGATC[A/G]CGCTACTGCACTCCA | 10138 |
rs113445537 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | YAF2 | GRCh38.p7 | 12:42222520 | TTTGATGAGCAAATA[G/T]AAGGATATATAGGAA | 10138 |
rs113514565 | snp | A/C | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42165810 | TTAATGTAACTAACT[A/C]CTCATCAACTGTCAT | 10138 |
rs113613091 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42227776 | CCCCGCCTGGCCAGC[A/C/G]TGCTGTCCGGGAGGG | 10138 |
rs113620053 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | YAF2 | GRCh38.p7 | 12:42175292 | CCATTCACATAAATT[C/T]CTAGAAAATGCAAAC | 10138 |
rs113747515 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | YAF2 | GRCh38.p7 | 12:42226126 | TCCTAGGTATTTTAT[C/T]CTCCTTGTAGCAATG | 10138 |
rs113764002 | snp | C/T | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42196145 | AAGAACTGCTTGAGC[C/T]CAAGAGGTGGAGGTT | 10138 |
rs113800947 | snp | C/T | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238585 | CCTCGCGCTCCAGAG[C/T]CCCTCTGAGGAGGAA | 10138 |
rs113844007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42230188 | CTCAAATCTGGGAGG[C/T]GGAGATTGCAGTGAG | 10138 |
rs113866817 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42161928 | CAATTTTAAAGATAT[A/G]TATCAGTTTTTCCCG | 10138 |
rs113885485 | snp | A/C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42228214 | GGGGGTCGGCCCCCC[A/C/G]CCCGGCCAGCCGCCC | 10138 |
rs113943409 | snp | C/T | 0.5 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42176275 | TACAGGAGTGCACCA[C/T]CACGCCAGCTAATTT | 10138 |
rs114001766 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | YAF2 | GRCh38.p7 | 12:42202496 | TTGTTTTTGAGCTTG[C/T]TATAAATGAAATCAT | 10138 |
rs114003211 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | YAF2 | GRCh38.p7 | 12:42191020 | ATTTTTTTCTCTTTA[C/T]AACAACAGAATGATA | 10138 |
rs114006062 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | YAF2 | GRCh38.p7 | 12:42167331 | TAAAATAGTTCCTAG[G/T]ATGTAATAGCAAACT | 10138 |
rs114039773 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | YAF2 | GRCh38.p7 | 12:42181472 | TAATGATCAGATCTG[C/T]GGCTCTTTGAATAAC | 10138 |
rs114047398 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | YAF2 | GRCh38.p7 | 12:42214687 | TGATTTTTTTTTGGT[A/T]TTTTTTTGTTTGCAA | 10138 |
rs114114285 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | YAF2 | GRCh38.p7 | 12:42206471 | AAAATTAAGTGGACG[C/T]GGTGGTGCACACCTG | 10138 |
rs114153362 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42168209 | TTGAAATGGAGCTTC[A/G]CTTTTGTTGCCCGGG | 10138 |
rs114204481 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | YAF2 | GRCh38.p7 | 12:42213946 | TAAAGGGCATTAATA[C/T]GCCCCATTATCTTTC | 10138 |
rs114212052 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42209126 | AACCAATTCTGTCAC[A/G]ATTCACATCAAGTAT | 10138 |
rs114212274 | snp | A/T | 0.0217236 | 0.101931 | intron-variant | YAF2 | GRCh38.p7 | 12:42174127 | AAAAACTCTTTCCTG[A/T]GTCTACATCCCTGTC | 10138 |
rs114275027 | snp | C/G | 0.00993419 | 0.0697739 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157490 | GAAGTTTAAAAAAGC[C/G]AGTGGCGGAAGCCTC | 10138 |
rs114284264 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | YAF2 | GRCh38.p7 | 12:42209726 | TCATAAAGAAATGTA[C/T]ACAAGAATTCAACAT | 10138 |
rs114311759 | snp | C/G | 0.0248432 | 0.108648 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42230883 | TTTAAAAAGGGCCAA[C/G]AACATCAAATACTTT | 10138 |
rs114351094 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42188730 | TCTAAGTATTCACAT[A/G]TACAATTTTATTATG | 10138 |
rs114382188 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | YAF2 | GRCh38.p7 | 12:42164721 | ATTGTGAATCTGTTG[A/G]TACTCTGGCTAACAA | 10138 |
rs114413712 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | YAF2 | GRCh38.p7 | 12:42224313 | TTCTGATAGGCCCTT[A/G]ATGTCAACTACCTTA | 10138 |
rs114426656 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | YAF2 | GRCh38.p7 | 12:42180580 | GTGAGATATAAATGT[C/T]GGTAAGTAGCTAAGT | 10138 |
rs114466833 | snp | A/G | 0.0766824 | 0.180169 | intron-variant | YAF2 | GRCh38.p7 | 12:42193032 | AGTATAGCACCTACC[A/G]GCCGGGCACGGTGGC | 10138 |
rs114479948 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | YAF2 | GRCh38.p7 | 12:42166447 | TGTCAAATATAGAAG[A/G]TAAAGAATGTTTTCA | 10138 |
rs114513282 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | YAF2 | GRCh38.p7 | 12:42199891 | CAAGTCAGAGTTCTT[C/T]GGCACATAACAATTC | 10138 |
rs114514297 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42183218 | CTTCTCCTTGAGCCT[C/G]CCTCTTCCCTGAGAC | 10138 |
rs114634429 | snp | G/T | 0.0441095 | 0.141807 | intron-variant | YAF2 | GRCh38.p7 | 12:42176367 | CTCAAGTGATACTCC[G/T]GCCTCAGCCACCCAA | 10138 |
rs114713945 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | YAF2 | GRCh38.p7 | 12:42220653 | TACCTCCCTGGCATA[A/C]AAATCATTTACTTGC | 10138 |
rs114734406 | snp | A/T | 0.0252325 | 0.109451 | intron-variant | YAF2 | GRCh38.p7 | 12:42184303 | ATTTCAACTTTAAAG[A/T]CTTATTATTATTATT | 10138 |
rs114743960 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | YAF2 | GRCh38.p7 | 12:42218870 | AAGATGAGTGGGGGG[A/G]AAAAAGGAAAGATAT | 10138 |
rs114848296 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | YAF2 | GRCh38.p7 | 12:42205672 | GCCACCGTGCCCGGT[A/C]ATTGCTGATTATTTT | 10138 |
rs114907925 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42170968 | GAGCACTAGAGCAAC[A/G]TAAGTGGTCAGGAAT | 10138 |
rs114953352 | snp | C/T | 0.0248432 | 0.108648 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239998 | GCTTGGGCGACAGAG[C/T]GAGACTCCGCCTCTA | 10138 |
rs114972132 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42236425 | ACGAAATATTTTATC[A/C]ATTGTGGGAATATAC | 10138 |
rs114977512 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42209421 | ATAAAAAAATTAGTC[A/G]AGCATGGTGGTGTGC | 10138 |
rs115048089 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | YAF2 | GRCh38.p7 | 12:42202218 | GAATCCATTTCTGAA[C/T]TCTCTATTAGTTTGT | 10138 |
rs115075227 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42169698 | GATTAGAGGTGTGAA[C/G]CACCGTGCCCAGCCA | 10138 |
rs115091934 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | YAF2 | GRCh38.p7 | 12:42204020 | CATGCCTGTGAATAG[C/T]CACTGCACTGCACTA | 10138 |
rs115263502 | snp | C/T | 0.021333 | 0.101051 | intron-variant | YAF2 | GRCh38.p7 | 12:42219564 | GAGATGCCCACATAC[C/T]CACATTCCTGTACAC | 10138 |
rs115324097 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42195693 | GGTGAAGACACAGTT[C/T]TGCCCTCAAAAAGGC | 10138 |
rs115333341 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | YAF2 | GRCh38.p7 | 12:42197540 | GTAGGGAAATGCCCA[A/C]TAATAATATGTATGC | 10138 |
rs115368961 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42231889 | TATATTTTTTGAATA[C/T]ATTCATTTTCAAGAA | 10138 |
rs115376511 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42188163 | TAATAAATCTGTTTA[C/T]CAAAAACATGTGAAA | 10138 |
rs115437894 | snp | A/G | 0.030278 | 0.119257 | intron-variant | YAF2 | GRCh38.p7 | 12:42208931 | AAGTTTTGTAAAACA[A/G]CTATAAGCAGGACAC | 10138 |
rs115477036 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42205237 | TTATAATTTTAAAAA[C/T]CACCATTATAGTTGT | 10138 |
rs115478698 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | YAF2 | GRCh38.p7 | 12:42210889 | ATTTTAAAAAGTCTA[C/T]TATAATGGCTGCTAT | 10138 |
rs115532276 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | YAF2 | GRCh38.p7 | 12:42179595 | AGGAGTTTGAGACCA[A/G]CCTAGTAACATGGTG | 10138 |
rs115598994 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42170845 | CCTCTCCAATAGTAT[A/C]ATTATTACCCATATT | 10138 |
rs115646103 | snp | A/G | 0.0185938 | 0.0946107 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157917 | GAGCCATCACACCCG[A/G]CCTATCTTCACTCTT | 10138 |
rs115647963 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42190457 | AAGATTGCTAGCTAG[C/T]CTTACTTTTAAAGGA | 10138 |
rs115656237 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42195120 | AAGTACATCCACTAA[C/G]TACTATTATGGGAGA | 10138 |
rs115657101 | snp | C/T | 0.0260105 | 0.111035 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42235536 | CTCTTAGGTTTAACT[C/T]AGAGCCAAAATCAAA | 10138 |
rs115673480 | snp | A/G | 0.021333 | 0.101051 | intron-variant | YAF2 | GRCh38.p7 | 12:42219142 | TGGCATAAATGACCT[A/G]GATGAAGTGAAGTGG | 10138 |
rs115695963 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42173161 | GCAATGGCACAGTCA[C/T]AGACACTGCAGCCTC | 10138 |
rs115704573 | snp | A/G | 0.136506 | 0.222754 | intron-variant | YAF2 | GRCh38.p7 | 12:42186017 | ACCAGCCTGACCAAC[A/G]TGGTGAAACCCCTAA | 10138 |
rs115706744 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | YAF2 | GRCh38.p7 | 12:42180317 | TAACAGAGTGGCCCA[C/T]GTGGCAAAGAACTGA | 10138 |
rs115707293 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | YAF2 | GRCh38.p7 | 12:42191535 | GCTAAGCTATATCAT[A/G]GGGCCTTTATACTTT | 10138 |
rs115709087 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42236238 | CCAACTCCAACCTTA[A/C]ACAGCCAAGAAGATA | 10138 |
rs115709313 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42206131 | TTTCTTTCTTCAAAT[C/T]AGTAACTTCTCTCTT | 10138 |
rs115760257 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42212946 | AGACTCCTAGTCACT[C/G]GAGTAAGTACATAGC | 10138 |
rs115829463 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42164270 | AGAAGGTATAAGTTT[C/T]GCAGTCTGTTGATTT | 10138 |
rs115838767 | snp | A/T | 0.0244538 | 0.107838 | intron-variant | YAF2 | GRCh38.p7 | 12:42236950 | AATAAAGTCTGAAAA[A/T]AGGCAGAGATCTTTT | 10138 |
rs115888771 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | YAF2 | GRCh38.p7 | 12:42182264 | AAATTCTGTTAACAT[A/G]TGATGTGGCCGGGTA | 10138 |
rs115910305 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | YAF2 | GRCh38.p7 | 12:42208930 | AAAGTTTTGTAAAAC[A/G]GCTATAAGCAGGACA | 10138 |
rs115954239 | snp | A/G | 0.0248432 | 0.108648 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42210330 | GGAAAAAAAATCTCA[A/G]GTTTGTGAAAACTAG | 10138 |
rs115954343 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | YAF2 | GRCh38.p7 | 12:42165073 | GAACAAAAAAAAAAA[A/G]AAAAAAGAAAAGAAA | 10138 |
rs116006172 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | YAF2 | GRCh38.p7 | 12:42165180 | AACATAGGCCCTGCC[C/T]TCATGCGCTAAAAAT | 10138 |
rs116014629 | snp | C/G | 0.0441095 | 0.141807 | intron-variant | YAF2 | GRCh38.p7 | 12:42176366 | CCTCAAGTGATACTC[C/G]TGCCTCAGCCACCCA | 10138 |
rs116019741 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | YAF2 | GRCh38.p7 | 12:42210975 | TCATTATATTTTATA[C/T]TAGTACAAGAATAAT | 10138 |
rs116074000 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | YAF2 | GRCh38.p7 | 12:42185046 | AGCTGGGCTTGGTGG[C/T]GCATGGCTGTAGACC | 10138 |
rs116079982 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | YAF2 | GRCh38.p7 | 12:42197277 | CCTTTGGCTATGAAC[C/T]CTCCTCTAACTCAAA | 10138 |
rs116164869 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | YAF2 | GRCh38.p7 | 12:42229549 | GACAATTATACTACA[A/G]TATATTTATTCTCCA | 10138 |
rs116258375 | snp | A/T | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42188155 | AAAATAGGTAATAAA[A/T]CTGTTTACCAAAAAC | 10138 |
rs116282737 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | YAF2 | GRCh38.p7 | 12:42173917 | TCCATCTGTACCGAC[A/G]TAGTCTGACTTCCCT | 10138 |
rs116286703 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | YAF2 | GRCh38.p7 | 12:42207194 | AGCAGTAGATTCAAA[A/G]CTAGTATTTAAGTCA | 10138 |
rs116286994 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42178611 | AGTTTGCTCCCATTT[C/T]CATTTTTATTTTTTA | 10138 |
rs116319646 | snp | A/G | 0.0299085 | 0.118574 | intron-variant | YAF2 | GRCh38.p7 | 12:42171516 | CTTTAAATTAAAAAA[A/G]AAAGAAAGAAAGAAA | 10138 |
rs116320655 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42198569 | CCAGCCTGGGCAATA[C/G]AGCGAGACCCTGTTT | 10138 |
rs116351272 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42235489 | AATTTCAGAAACCAC[C/T]AGGAAAATAACAGAT | 10138 |
rs116412260 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42168675 | TCTCCTTTAAAAAAA[C/G]AAGAACACTCCATTC | 10138 |
rs116504260 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42204447 | CTAAGCAATACAATA[C/T]AACAACTATTTACAT | 10138 |
rs116507825 | snp | C/T | 0.0232847 | 0.105357 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42210236 | ATAATCCATATCAAA[C/T]GTACAAAAAGAAGCT | 10138 |
rs116539383 | snp | C/T | 0.0248432 | 0.108648 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42240227 | TGGTACACCGATAAA[C/T]CCATCGTAAAGTAGA | 10138 |
rs116719257 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42170312 | GCATTCAACAAATGA[C/T]TGCTGAATGAATTAA | 10138 |
rs116753453 | snp | A/T | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42188729 | TTCTAAGTATTCACA[A/T]GTACAATTTTATTAT | 10138 |
rs116812782 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | YAF2 | GRCh38.p7 | 12:42202105 | GCAGAGATCTAGTTT[C/T]CCCCCCCATCTAGAA | 10138 |
rs116814812 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | YAF2 | GRCh38.p7 | 12:42172006 | ATTTAGGCTCCTCAA[A/C]AAACCAGCCTCTAAC | 10138 |
rs116882902 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42225284 | TCAGATGGACAGATG[A/G]CAAAAATATTCTCCA | 10138 |
rs116915417 | snp | A/G | 0.0142736 | 0.0832652 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42158365 | TAGGTCATCCAAGAG[A/G]GCAGGAAAATAACTG | 10138 |
rs116959789 | snp | G/T | 0.0165278 | 0.0893908 | intron-variant | YAF2 | GRCh38.p7 | 12:42223553 | TATTTGTACAGACAG[G/T]GTCTCGCTATGTTGC | 10138 |
rs116964620 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | YAF2 | GRCh38.p7 | 12:42183804 | AAAAAAGCATTATTG[A/C]AAGAAGATGCCATCT | 10138 |
rs117186296 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | YAF2 | GRCh38.p7 | 12:42224066 | AAATAAATAATAATG[A/G]CCACAACAATAACTG | 10138 |
rs117218456 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | YAF2 | GRCh38.p7 | 12:42165322 | CAGGTATCACAATGG[A/G]CCCTTTTAATAAGAG | 10138 |
rs117269595 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | YAF2 | GRCh38.p7 | 12:42170111 | TCCTGAGGTCAAGCA[A/G]TCCTCCTGCCTCAGC | 10138 |
rs117328117 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | YAF2 | GRCh38.p7 | 12:42215442 | AAAAAAACTCCAGTG[G/T]ACTTCAGAGATAGCT | 10138 |
rs117387064 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | YAF2 | GRCh38.p7 | 12:42219122 | AATCCTAATAAAATA[C/T]ATAATGGCATAAATG | 10138 |
rs117418879 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233176 | GTGTAACATCTAGCA[C/T]TCTTTCTACTATGTG | 10138 |
rs117422274 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | YAF2 | GRCh38.p7 | 12:42219667 | GGGAAAAGCTCTTTG[A/G]AAAAGGCAGCTCAAA | 10138 |
rs117493617 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | YAF2 | GRCh38.p7 | 12:42220844 | ATCCAGTCATTCACA[C/T]ATTCACATATTATCA | 10138 |
rs117503242 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | YAF2 | GRCh38.p7 | 12:42176456 | TCCCTTCTCCCACTC[C/T]TCCAATCTTCAACAA | 10138 |
rs117512620 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | YAF2 | GRCh38.p7 | 12:42236126 | ATTGTTTCCACTTTA[A/C]TGTTCCTGCCTCCAA | 10138 |
rs117527912 | snp | A/G | 0.0532157 | 0.154195 | intron-variant | YAF2 | GRCh38.p7 | 12:42189906 | AAACAGGTCAATAGC[A/G]TATGTATTCACTACA | 10138 |
rs117538962 | snp | A/G | 0.0532157 | 0.154195 | intron-variant | YAF2 | GRCh38.p7 | 12:42166205 | GGCATGAGCCATTGC[A/G]CCTGGCCTCAAATAC | 10138 |
rs117543576 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42215467 | ATAGCTGTTACTTTA[C/T]AGAACAAATGAAGTT | 10138 |
rs117563952 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | YAF2 | GRCh38.p7 | 12:42217676 | AAAAAATCACATGAA[C/T]ATAAATGTCAAGGAG | 10138 |
rs117591929 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42223020 | ATTATCTGTCACTTG[C/T]GCAGTGCTTTACTGT | 10138 |
rs117889310 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | YAF2 | GRCh38.p7 | 12:42202447 | TTCCAAGATGACCAC[A/G]ATTCTCATCTCTATC | 10138 |
rs117929500 | snp | G/T | 0.0618563 | 0.164627 | intron-variant | YAF2 | GRCh38.p7 | 12:42194376 | CGGCCAGGCAGGATG[G/T]CTCACGCCTGTAATC | 10138 |
rs118009138 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | YAF2 | GRCh38.p7 | 12:42189503 | GACAGACTGGGAGCA[A/G]GGAGAACCATTAGGG | 10138 |
rs118022794 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42220369 | CCCCACACCCAGATT[A/C]TTTACATTAGCATTT | 10138 |
rs118045082 | snp | C/T | 0.0310518 | 0.120672 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233712 | GAGACGAGATCTCAC[C/T]GTGTTGCCCAGGTTG | 10138 |
rs118132513 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | YAF2 | GRCh38.p7 | 12:42169785 | ATGACACTATTGGAG[C/T]GGTGGAGCTACAAGA | 10138 |
rs118189377 | snp | C/G | 0.00326797 | 0.0402902 | intron-variant | YAF2 | GRCh38.p7 | 12:42212509 | CAAAGAAAGTGTATA[C/G]TTTTTCCTTTAAGAA | 10138 |
rs137872761 | snp | A/G | 0.000496722 | 0.0157516 | synonymous-codon, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160688 | AGAGCCGCTTTGACT[A/G]TGTTGATCTGCAGAA | 10138 |
rs137882252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42201217 | TTGGGCAACTGTTCA[A/G]GTTTCTCTAGACTAA | 10138 |
rs137926859 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42167435 | GGTCCATATGGTAAT[C/T]TCAAAAAATAAATGT | 10138 |
rs137959259 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | YAF2 | GRCh38.p7 | 12:42178927 | GTGTGGTGGTGCGTG[C/T]CTGTAGTCTTACGTA | 10138 |
rs137966648 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42211597 | TAAAAATACAAAAAG[G/T]AGCCAGGTGTGGTGG | 10138 |
rs137975924 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42209397 | GGCAAAACCCCATCT[C/T]TATAAAAAATAAAAA | 10138 |
rs138018179 | in-del | -/A | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42186341 | CCTAGGTGACCGAGC[-/A]AAAACTCCAACTCAA | 10138 |
rs138069045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42217697 | TGTCAAGGAGGGGAT[C/T]TAAACTGAAATGTGA | 10138 |
rs138141134 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42231261 | AAACTTATTATTTTC[C/T]AAAACAAAGATATTT | 10138 |
rs138144742 | in-del | -/AAAT | | | intron-variant | YAF2 | GRCh38.p7 | 12:42215928 | AGATTCCAGCTCAAA[-/AAAT]AAATAAATAAATAAA | 10138 |
rs138202029 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | YAF2 | GRCh38.p7 | 12:42180513 | GTATCAGGAGATCCT[A/G]AATCAGAGGACCCAG | 10138 |
rs138262347 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42156910 | TATTATTTTCCTTAC[A/G]TACGCACTCACTTTT | 10138 |
rs138318045 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | YAF2 | GRCh38.p7 | 12:42194874 | TAGAAGACACACAAA[C/T]GAAGCTGTGTAACTC | 10138 |
rs138356767 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42189215 | TGCTAGTAAATAATC[A/G]ACTACAACTGCATAC | 10138 |
rs138399006 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | YAF2 | GRCh38.p7 | 12:42207683 | AGATCACAAGGTCAG[A/G]CGATCAAGACCATCC | 10138 |
rs138453565 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | YAF2 | GRCh38.p7 | 12:42166441 | TTTTTGTGTCAAATA[C/T]AGAAGATAAAGAATG | 10138 |
rs138501470 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233050 | ACCACTGTATGTCTA[A/G]TATCCAACTCAGCCC | 10138 |
rs138524262 | snp | C/G | 0.0444908 | 0.142359 | intron-variant | YAF2 | GRCh38.p7 | 12:42164749 | CAAACGCCCAAAAAT[C/G]TAACCTAGGAAAGAT | 10138 |
rs138624130 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | YAF2 | GRCh38.p7 | 12:42176790 | AATATGGCGAAACCC[C/T]GTCACCACTAAAAAT | 10138 |
rs138681985 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42175605 | CGGGAGGCCAGGCAC[A/G]GTGGCTCACGCCTGT | 10138 |
rs138692837 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42179536 | AATCTGAAGGTCTAA[C/G]TTTTCTAAAAATAGA | 10138 |
rs138701556 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | YAF2 | GRCh38.p7 | 12:42171180 | CATTTTTAGTAGAGA[C/T]GGGATTTCACCATAT | 10138 |
rs138716230 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | YAF2 | GRCh38.p7 | 12:42188799 | TTGAGACGCTATTCA[C/T]TTCAAAGCTTCTATT | 10138 |
rs138732051 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42225693 | AGATGGTTGTAGATA[A/C]GTGGTGTTATTTCTG | 10138 |
rs138812312 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | YAF2 | GRCh38.p7 | 12:42223100 | TATGAGACTGGTGAA[A/G]AAGGTAGAAATCCAG | 10138 |
rs138818732 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42215096 | ACCTAGCCCAGCACC[A/T]GTCTCAAAATACCAT | 10138 |
rs138994249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42205711 | CCAAATTCTGTTTTC[A/G]TTTTTATTATTTCCT | 10138 |
rs139065959 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238925 | TCAAGACTCAAGAGA[A/G]ATTAGGTGACTTCCT | 10138 |
rs139107900 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42231626 | ACCCATTACAGTTTT[A/G]TAAAATCATACATCG | 10138 |
rs139130696 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | YAF2 | GRCh38.p7 | 12:42196082 | CAAAAATTAGCAGGG[C/T]GTGGTGGCACATGCC | 10138 |
rs139138822 | in-del | -/A | 0.168135 | 0.236216 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239155 | CGTCAACATACTAAA[-/A]GGTCCTCATACTCCA | 10138 |
rs139145262 | snp | G/T | 0.00478085 | 0.0486577 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42158669 | CCGTGTTCCCGTCTA[G/T]GTAGAAAGATGAGTA | 10138 |
rs139163036 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42171522 | ATTAAAAAAAAAAGA[A/C]AGAAAGAAAGAAATA | 10138 |
rs139286746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42223489 | CTGGAAATTGGCCAT[A/G]ATGTTAAAGCACATT | 10138 |
rs139460975 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | YAF2 | GRCh38.p7 | 12:42192406 | CCCACCTACTCAGGA[A/G]GCTGAGTTGATAGGA | 10138 |
rs139516045 | in-del | -/GGGG | | | intron-variant | YAF2 | GRCh38.p7 | 12:42217138 | TAAAATCTGTCGGCT[-/GGGG]GTGGTTTCAATCATA | 10138 |
rs139517162 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42196430 | CATGAAACGATTTGC[A/C]AGCCATGTTAAGAAG | 10138 |
rs139544104 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42177140 | CTGGCAACCAGAGTA[C/T]ATGGCAATCAACAAA | 10138 |
rs139584654 | snp | C/G | 0.136506 | 0.222754 | intron-variant | YAF2 | GRCh38.p7 | 12:42173066 | AGAGAGAGAGAGGGA[C/G]AGAGAGAAAGAGAGA | 10138 |
rs139659331 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | YAF2 | GRCh38.p7 | 12:42208267 | TGTCTCTACTAAATA[A/T]ACAAAAAAGCTAGCC | 10138 |
rs139711101 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42169337 | TTATATCTAAACTGG[A/C]TCCTCTTAGAACTTC | 10138 |
rs139732897 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | YAF2 | GRCh38.p7 | 12:42182488 | GAAAAGTTATTTCTA[A/G]TAGAGTGAAACTATA | 10138 |
rs139827747 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157621 | ACTTAGAAAGGCTGA[A/C]GTTTCTCTTCCTTTT | 10138 |
rs139849170 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42235051 | CAATCTTCTCTGCAG[G/T]TCTAAAAAGAAAAAA | 10138 |
rs139878172 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42226843 | TTAAATAGACATCTT[A/G]AGAGGAGGTCGCGGC | 10138 |
rs139992728 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234478 | AATATACCCAAGTAA[A/C]AAACATGCACATGTA | 10138 |
rs140042499 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42218541 | TTTAAAAAATGTATT[A/T]TTTTTTCCAGAATAC | 10138 |
rs140063332 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | YAF2 | GRCh38.p7 | 12:42212694 | TATTTGTATTTGTTA[A/G]GTTGACAACACACCT | 10138 |
rs140079269 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | YAF2 | GRCh38.p7 | 12:42186117 | AATTGCTTGAACCCA[A/G]GAGGCAGAGGTTGCA | 10138 |
rs140122474 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | YAF2 | GRCh38.p7 | 12:42182889 | GCATGAACACAAGAG[C/T]ACATCTCATTTTATT | 10138 |
rs140125752 | snp | A/G | 0.000281334 | 0.011857 | synonymous-codon, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160628 | TGAGGCTTCTCCTCT[A/G]GGTGAAGATGACCTG | 10138 |
rs140138004 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42211521 | GCAGGTGGATCACCT[C/G]AGGTTGGGAGTTCAA | 10138 |
rs140202027 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | YAF2 | GRCh38.p7 | 12:42224541 | TAGCCCCCCACCCCG[C/T]GACAGGCCCCCGTGT | 10138 |
rs140289497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42187680 | TAAAATATATATAGC[A/G]TGAAAATACCTTAAT | 10138 |
rs140363055 | snp | C/T | 0.00162206 | 0.0284323 | intron-variant, utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42235783 | AAAAATGTCAGGGGC[C/T]CCCATGTGGGCCTCA | 10138 |
rs140363089 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | YAF2 | GRCh38.p7 | 12:42184559 | AGGTGATTGACTCAC[C/T]GCAGCCTCTCAAAGT | 10138 |
rs140381576 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | YAF2 | GRCh38.p7 | 12:42230544 | GATAATGAAGATCAT[A/G]TTAGTAGCATTCCAA | 10138 |
rs140396291 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | YAF2 | GRCh38.p7 | 12:42165902 | TCTATCTATCTATCT[A/G]TCTGTCTATATCTAT | 10138 |
rs140398519 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | YAF2 | GRCh38.p7 | 12:42194116 | GAAAACATTAAAAAA[A/C]TTAATACTAAGCTCA | 10138 |
rs140503120 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | YAF2 | GRCh38.p7 | 12:42199037 | TGACTATTTTAACAT[C/T]TTTGTTGAATTTAAT | 10138 |
rs140531958 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | YAF2 | GRCh38.p7 | 12:42165624 | GCCTGCCACCATGCC[C/T]GGCTAATTTTTTTTT | 10138 |
rs140573616 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42213234 | TGGCCAACAGCCAGA[A/T]GCCTGAGGCCTGACA | 10138 |
rs140574281 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42209133 | TCTGTCACAATTCAC[A/G]TCAAGTATTTTCATT | 10138 |
rs140611093 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42203382 | AATATTTCTAGGGAG[C/T]ATCTCATCTCATTTC | 10138 |
rs140612647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42169432 | TCTTTTCTTTTTTTT[C/T]GGAGACATAGTCTCA | 10138 |
rs140686502 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | YAF2 | GRCh38.p7 | 12:42166338 | GAGACAGACATTCTC[C/T]CTGCTTCAGAATTAC | 10138 |
rs140706450 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42210194 | CCCATTAATAGCTCA[G/T]TATTTACTGTCCACA | 10138 |
rs140721450 | in-del | -/AG | | | intron-variant | YAF2 | GRCh38.p7 | 12:42179065 | CTCTTTCAAAAAGAA[-/AG]AAAAAATACACTTGT | 10138 |
rs140761483 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42183827 | TGCCATCTAGGACTT[A/T]CAGAGCTAGAGACGA | 10138 |
rs140892185 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238570 | GGCTGCCGGGGACTG[C/T]CTCGCGCTCCAGAGC | 10138 |
rs140962363 | in-del | -/AAG | 0.0217236 | 0.101931 | intron-variant | YAF2 | GRCh38.p7 | 12:42182126 | ATTATTTCACAAAAA[-/AAG]AAGGTTAAAACTACA | 10138 |
rs140996356 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | YAF2 | GRCh38.p7 | 12:42162164 | AAGGAAATACCTGAC[C/T]ATTTGTGACAATGGC | 10138 |
rs141024619 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42183350 | CTAGAAATGATTAAG[C/G]TTAGTGAGGAAGGCA | 10138 |
rs141061400 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42225475 | TCAGGACATAAAACC[A/T]TGCCTAGGTTTCCTT | 10138 |
rs141082742 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42219712 | TCACACCCCGTCCAC[A/C]TCATTATCTTATCCA | 10138 |
rs141168685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42178145 | AATAAAGAAAAATAA[A/G]TATTTAATGTTTTTA | 10138 |
rs141209311 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42176018 | CTGGGAGGCCAAGGC[A/G]GGTGGATCACTTGAG | 10138 |
rs141217073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42202078 | GGAATTTATTTTCAC[A/G]TATTGCTTGAAGCAG | 10138 |
rs141233810 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | YAF2 | GRCh38.p7 | 12:42215765 | TGTCTCTACTAAAAA[C/T]ACCAAAAAACATTAG | 10138 |
rs141303310 | snp | A/G | 0.0513262 | 0.151752 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42209979 | AATTTTCTATTTTTC[A/G]TAGAGACAGGGTTTC | 10138 |
rs141305278 | in-del | -/AT | 0.21725 | 0.247846 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157779 | CATATATATATATAT[-/AT]GTATATTCAAATTTT | 10138 |
rs141374745 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | YAF2 | GRCh38.p7 | 12:42205446 | AGTGGCACAATCTCA[G/T]CTCACTGCAACCTCC | 10138 |
rs141461696 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42185998 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGACC | 10138 |
rs141567351 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | YAF2 | GRCh38.p7 | 12:42192130 | TAAGGCTGGAGAATA[C/T]TGAATATGGAGAAAA | 10138 |
rs141578434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42161597 | AAAAATGTCATAAAA[C/T]ACTCTTCACATTTAC | 10138 |
rs141633623 | snp | C/G | 0.0248432 | 0.108648 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239740 | TTGGCCGGTTGCGGT[C/G]GCTCACGCATGTAAT | 10138 |
rs141650008 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | YAF2 | GRCh38.p7 | 12:42170268 | CTTTTCATTTTTGAA[A/G]CACTGGTAACAAGCT | 10138 |
rs141758953 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42176314 | TAAATAGAGATGGGG[C/T]TTCACCATGCTGGCC | 10138 |
rs141780277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42222611 | AAATTTATATATATT[C/T]AATACTTGAAAAATC | 10138 |
rs141827212 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42180048 | TCCTAAGTTTCTTTC[A/G]TTTGTTTCATTAACT | 10138 |
rs141830324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42177547 | GGACTCCACTTTTAC[A/G]AGTTCATTTAATCTT | 10138 |
rs141864560 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | YAF2 | GRCh38.p7 | 12:42226047 | TTGTGTCCTCTCTTA[C/T]TTCCTTGAGCAGTGG | 10138 |
rs141866452 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | YAF2 | GRCh38.p7 | 12:42176791 | ATATGGCGAAACCCC[A/G]TCACCACTAAAAATA | 10138 |
rs141884357 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42226240 | CTATATTATATCATA[C/G/T]AAATTTCAACTATCT | 10138 |
rs141948148 | in-del | -/TG | 0.00517822 | 0.0506191 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232997 | TCTAATTTGCAAAAC[-/TG]TAAAATTTTAAAGAA | 10138 |
rs142005849 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233192 | TCTTTCTACTATGTG[A/C]AATCTTTTTTATAGC | 10138 |
rs142013099 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42166624 | TTTGAGAAAAATGAA[C/G]AAGGATATTGTCATC | 10138 |
rs142040368 | snp | G/T | 0.079617 | 0.182947 | intron-variant | YAF2 | GRCh38.p7 | 12:42214934 | GTTTGAACCTGGGAG[G/T]CAGAGGTTGCAGTGA | 10138 |
rs142107082 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157997 | TTGTATGGAATTTGG[C/T]TAAAAGAACCCAGTG | 10138 |
rs142109253 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42187451 | AGCCCACCTTGTTTT[C/T]ATTATTGAAGATGTA | 10138 |
rs142220463 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42193993 | AGTAAAAAAATTTTT[G/T]AATGGAGAAAGCACA | 10138 |
rs142224265 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | YAF2 | GRCh38.p7 | 12:42163758 | TCAAATAAAGTTCTC[C/T]GCTGCTCTCTAGGAG | 10138 |
rs142231775 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42209304 | AGCAGTGGCTCACAC[C/T]TGTAATCCCAACACT | 10138 |
rs142237287 | snp | C/T | 0.000128321 | 0.00800901 | intron-variant | YAF2 | GRCh38.p7 | 12:42160870 | TAGCTTTTCCCTCTA[C/T]CAAATTTCTGAGCAT | 10138 |
rs142252797 | in-del | -/CCGC/GGTGGCCGC/GGTGGCCGCGGTGGCCGC | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238473 | GGCGGGCGGTGCGGG[lengthTooLong]GGTGGCCGCGGTGGC | 10138 |
rs142301889 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42201438 | CTGCTAATTGCCTTT[A/G]TATCCATTGTTCATT | 10138 |
rs142369189 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | YAF2 | GRCh38.p7 | 12:42198107 | GTGAAATGTTGGGCC[A/T]CACCTTATAAAAAAA | 10138 |
rs142378084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42177417 | ACATTTCCTTCTGGC[C/T]TACAGACGGCCATGT | 10138 |
rs142407290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42194897 | TGTAACTCTCTAATA[A/G]TTCACATGTAAATAA | 10138 |
rs142489401 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42183540 | GTTTCAGCTTGGATA[G/T]AAGATCAAACCAGTC | 10138 |
rs142571469 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42165502 | TGAGCCTAGCTCTGT[C/T]GCCCAGGCTGGAGTG | 10138 |
rs142572370 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42209561 | AGAGCCAGACTTTGT[C/T]TCAAAAAAAAAAAAA | 10138 |
rs142651413 | in-del | -/AC | | | intron-variant | YAF2 | GRCh38.p7 | 12:42170675 | CAAACAAAAAACTAT[-/AC]ACACACACACACACA | 10138 |
rs142686643 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42237080 | TTATTTATAAAATAT[G/T]AGAGTACTGGAATAA | 10138 |
rs142716436 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | YAF2 | GRCh38.p7 | 12:42168461 | TGCTGGGATTATAGA[C/T]GTGAGCCACCATGCC | 10138 |
rs142753835 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42212557 | CACCACTGAATAAAT[A/G]AAAGAAAACAAAACA | 10138 |
rs142761178 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | YAF2 | GRCh38.p7 | 12:42171230 | TCCTGACCTCAAGTG[A/T]TCCGCCCACCTTGGC | 10138 |
rs142810401 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | YAF2 | GRCh38.p7 | 12:42181740 | ATAATGCTGTGAAAG[C/T]AAACAATAAACAAGG | 10138 |
rs142837233 | snp | C/G | 0.0360663 | 0.129354 | intron-variant | YAF2 | GRCh38.p7 | 12:42168286 | TGGGTTCAAGTGATT[C/G]TCCTGCCTCAGCCTC | 10138 |
rs142901101 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | YAF2 | GRCh38.p7 | 12:42219644 | CACATGCACACACAA[A/T]AATGTGAGGGAAAAG | 10138 |
rs142901999 | in-del | -/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42180028 | TACTAGTACAAAGTA[-/T]TTTTTCCTAAGTTTC | 10138 |
rs142990626 | in-del | -/TTTG | 0.00209161 | 0.0322712 | intron-variant | YAF2 | GRCh38.p7 | 12:42205917 | TTTTGTAATTTCCAT[-/TTTG]TTTTTTAATTCTTGA | 10138 |
rs143037593 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42200217 | CACTGCCTGCTTCCC[A/G]TGCTCCAAATCAAGA | 10138 |
rs143074588 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | YAF2 | GRCh38.p7 | 12:42196039 | CCAGCCTGGCCAACA[C/T]GGTGAAACCCCATCT | 10138 |
rs143112872 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42179267 | CTGAGGTCAGGAGTT[C/T]GAGATCAGCCTGGCC | 10138 |
rs143170052 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | YAF2 | GRCh38.p7 | 12:42226856 | TTGAGAGGAGGTCGC[A/G]GCGCCGGAGGCCCCA | 10138 |
rs143238714 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42231619 | ATGGATTACCCATTA[C/T]AGTTTTGTAAAATCA | 10138 |
rs143297092 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42235309 | GAATTATTTCTTCCA[A/T]CTACTGAAACTTTTG | 10138 |
rs143304856 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | YAF2 | GRCh38.p7 | 12:42166146 | TTGAACGCCCAACCT[C/T]AGGTGATCCGCCTGT | 10138 |
rs143539230 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | YAF2 | GRCh38.p7 | 12:42172639 | GTGAATAAATCAAGT[A/T]CATACCCAAGAGAAA | 10138 |
rs143541338 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | YAF2 | GRCh38.p7 | 12:42211617 | AGGTGTGGTGGCATG[C/T]GCCTGTAATCCCAGC | 10138 |
rs143579700 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42208377 | GTTGCAGTGAACGGA[G/T]ATCATGCCACTGCAC | 10138 |
rs143602849 | in-del | -/TTATC | | | intron-variant | YAF2 | GRCh38.p7 | 12:42220325 | TCATGAGAAAAAGAA[-/TTATC]TTAAGGAAAAAATAA | 10138 |
rs143685290 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42169363 | ACTTCCTCTTCCAGC[A/C]CCTTTAATGTTGAGG | 10138 |
rs143687214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42218574 | TTTTGGGATTTTGAC[C/T]TTTCAGGATTGTGAT | 10138 |
rs143703386 | snp | C/T | 0.000533484 | 0.0163235 | intron-variant | YAF2 | GRCh38.p7 | 12:42161805 | TATTTTAAATTACAA[C/T]TTAAAACATAAGTGC | 10138 |
rs143724381 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | YAF2 | GRCh38.p7 | 12:42203979 | AAATTGCTTGAGGCC[A/C]GTTTGAAGCTGCAGT | 10138 |
rs143838007 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | YAF2 | GRCh38.p7 | 12:42211414 | CCTGGATGACAGAGC[A/G]AGACTCTGTCTCCAA | 10138 |
rs143864583 | in-del | -/T | 0.0524604 | 0.153226 | intron-variant | YAF2 | GRCh38.p7 | 12:42174891 | AGTAATGAACATTAA[-/T]TTTTAATAATGAAAG | 10138 |
rs143879123 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42201488 | CTTTTGATCTTTATA[C/T]AGTCTGGACACAAAT | 10138 |
rs143879521 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42235009 | GAAAAAAGAAAAAAA[A/G]AAGACTTCAAAGGTA | 10138 |
rs143923103 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42190032 | AATGCCATAACAATT[C/T]ACTTTTGTCGTTTTA | 10138 |
rs144037695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42196086 | AATTAGCAGGGTGTG[A/G]TGGCACATGCCTGTA | 10138 |
rs144060115 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | YAF2 | GRCh38.p7 | 12:42193271 | AGTGAACCGAGATTG[C/T]GCTGCTGCACCCCAG | 10138 |
rs144167914 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | YAF2 | GRCh38.p7 | 12:42224548 | CCACCCCGCGACAGG[C/T]CCCCGTGTGTGATGT | 10138 |
rs144187352 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42171679 | TCATATCTGGCTGGG[C/T]GTGGTAGCTCACGCC | 10138 |
rs144261254 | in-del | -/AAATAAATAAAT | | | intron-variant | YAF2 | GRCh38.p7 | 12:42215928 | AGATTCCAGCTCAAA[-/AAATAAATAAAT]AAATAAATAAATAAA | 10138 |
rs144276403 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | YAF2 | GRCh38.p7 | 12:42177239 | CTCTTCTATATGGCA[C/T]CCATTATTCCAGTGT | 10138 |
rs144305784 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | YAF2 | GRCh38.p7 | 12:42177275 | TCTGCTTGGGCTGTC[A/G]TAACAAAATACCATA | 10138 |
rs144318564 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42173082 | AGAGAGAAAGAGAGA[C/G]TCTGGAGTAAAAATT | 10138 |
rs144340715 | snp | C/G | 0.00874735 | 0.0655527 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157455 | TTTGGTGAGGACAAA[C/G]CATATCCAAACCATA | 10138 |
rs144448961 | in-del | -/AGA/GA | 0.247337 | 0.249986 | intron-variant | YAF2 | GRCh38.p7 | 12:42218182 | ACATCAGGCTACTAG[-/AGA/GA]GAAACACACACACAC | 10138 |
rs144498321 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | YAF2 | GRCh38.p7 | 12:42165661 | TATTTTTAATAGAGA[C/T]GGGGTTTCACTGTGT | 10138 |
rs144515401 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | YAF2 | GRCh38.p7 | 12:42208154 | GCAATATGGCCAGGC[A/G]CCATGGCTCATGCCT | 10138 |
rs144536081 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42161073 | TAGAACTTGTGCTTC[G/T]ATAGCTGTATCATAA | 10138 |
rs144650870 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | YAF2 | GRCh38.p7 | 12:42211878 | ACATAGTGAAACCCC[A/G]TCTCTACTAAAAATA | 10138 |
rs144775935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42182858 | ATATCAGGACATACA[A/G]TGAAAATCTTGAATA | 10138 |
rs144777834 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | YAF2 | GRCh38.p7 | 12:42225629 | ACACCATTTATTAAA[C/T]AGGGAATCCTTTCCC | 10138 |
rs144786312 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | YAF2 | GRCh38.p7 | 12:42195900 | TGGGGAAGAGTGGAA[C/G]GCAGGAGTTGCGGGG | 10138 |
rs144831644 | in-del | -/T | 0.0509478 | 0.151255 | intron-variant | YAF2 | GRCh38.p7 | 12:42204102 | AAAAAAATCTATCCC[-/T]TCTGACACCACTTCA | 10138 |
rs144836947 | in-del | -/ATTG | 0.0352966 | 0.128072 | intron-variant | YAF2 | GRCh38.p7 | 12:42198727 | GGGTTTCAGACTACA[-/ATTG]ATTAATAGTTAAGAT | 10138 |
rs144881216 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | YAF2 | GRCh38.p7 | 12:42186937 | TTGCCACCAATTCAG[C/T]GAACTATAATTTTAA | 10138 |
rs144916546 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42224115 | CTTCTCCAAAAACTA[C/G]AACTATGTTGGAAAA | 10138 |
rs144925821 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42222989 | GTTGGAAACTCAGTA[A/G]AAAGCTGTGTCTTTC | 10138 |
rs144953072 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | YAF2 | GRCh38.p7 | 12:42220017 | AAAACAAACTGGAGC[A/C]TTCTCAGAGACTGGA | 10138 |
rs144996598 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | YAF2 | GRCh38.p7 | 12:42225439 | GAAGTCTTTGCCCAT[A/G]CCTATGTCCTGAATA | 10138 |
rs145092392 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42209986 | TATTTTTCGTAGAGA[C/G]AGGGTTTCTCCATGT | 10138 |
rs145110893 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | YAF2 | GRCh38.p7 | 12:42205585 | TCACCATCTTGGCCA[A/G]GCTGGTCTTGAACTC | 10138 |
rs145185764 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42201191 | AAATGAATATCCATG[C/T]ACATTCCTCCTTGGG | 10138 |
rs145205182 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | YAF2 | GRCh38.p7 | 12:42165974 | CCAGGCTGGAGTGCG[A/G]TGGCGTGATCTTGGC | 10138 |
rs145233312 | in-del | -/CAAA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42185177 | AGCCAGACTTTGTCG[-/CAAA]CAAACAAACAAACAA | 10138 |
rs145248919 | in-del | -/AC | 0.0252325 | 0.109451 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42235560 | ATCAAAAGAGAAGAG[-/AC]AATTCAGAGAGAGGA | 10138 |
rs145290863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42203323 | CCTTGTATCCAGCAA[C/T]GCTGAATTATTTTAT | 10138 |
rs145380623 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42214336 | GAGTGCAGTGGCACA[A/G]TCTCAGCTCACTGCA | 10138 |
rs145407040 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42187688 | ATATAGCATGAAAAT[A/G]CCTTAATATATTGTC | 10138 |
rs145492039 | snp | C/T | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42221607 | TCAGATTTCTAAATC[C/T]CACACTGATCAACTA | 10138 |
rs145553932 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YAF2 | GRCh38.p7 | 12:42184997 | ATCTGGCCAATATGG[C/T]GCAACCCTGTCTCTA | 10138 |
rs145574483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42196909 | TGATGAGTCTGACTG[A/G]GACCTCAAGGCAGTG | 10138 |
rs145654938 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | YAF2 | GRCh38.p7 | 12:42182895 | ACACAAGAGCACATC[A/T]CATTTTATTGTGCAT | 10138 |
rs145694091 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | YAF2 | GRCh38.p7 | 12:42177605 | AATACAGTCACATAG[A/C/G]GGGTGAGGGCTTCAT | 10138 |
rs145734548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42175265 | GACCAAAAAAATACA[C/T]ACTGTATGATTCCAT | 10138 |
rs145752353 | snp | G/T | 0.0376037 | 0.131863 | intron-variant | YAF2 | GRCh38.p7 | 12:42169461 | CACTGTCCCCCAGGC[G/T]GGAGTGCATTGGCAC | 10138 |
rs145771714 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42220771 | AAAGATGAAATTGTT[G/T]AATTCATATGTCTAA | 10138 |
rs145792067 | in-del | -/AAAG | 0.00996189 | 0.0698692 | intron-variant | YAF2 | GRCh38.p7 | 12:42230262 | CTCCTTCAAGAAAGA[-/AAAG]AAAGAGAAGAAAGAG | 10138 |
rs145860938 | snp | A/G | 0.000153988 | 0.00877327 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42237705 | CCTCATCCGAGGACG[A/G]CTTCGGCTGCCGCTT | 10138 |
rs145866111 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42171105 | TCAAGCAATCCTCCT[A/G]CCTCAGCCTCCCAAG | 10138 |
rs145889173 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42175031 | CCCTTTCAATATATG[A/T]ACTCAAAGAAGGAAA | 10138 |
rs145894715 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | YAF2 | GRCh38.p7 | 12:42166408 | GCATCTGTCCACTAA[C/T]GAACTATCTCAAGTA | 10138 |
rs145899459 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | YAF2 | GRCh38.p7 | 12:42215055 | TGAGAGTAAAAATGT[A/G]TCTTGTTCTCCTCTG | 10138 |
rs145931569 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157579 | TCTATAAGGATCTTT[A/C]TCTAAAAGTTAATAA | 10138 |
rs146054373 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42218472 | AAAGTGGCCTATGAA[C/T]TGTTGTTTTTATCTG | 10138 |
rs146064846 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42212691 | TCATATTTGTATTTG[G/T]TAGGTTGACAACACA | 10138 |
rs146173833 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | YAF2 | GRCh38.p7 | 12:42196080 | CACAAAAATTAGCAG[G/T]GTGTGGTGGCACATG | 10138 |
rs146283413 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | YAF2 | GRCh38.p7 | 12:42180482 | CAGCCCCAGCCACAA[C/T]GCTGACTGCAGCCTT | 10138 |
rs146293543 | snp | A/G | 0.0626037 | 0.165477 | intron-variant | YAF2 | GRCh38.p7 | 12:42176882 | TAAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG | 10138 |
rs146482342 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | YAF2 | GRCh38.p7 | 12:42193632 | CCACCTCAGCCTCCT[A/G]AGTAGCTAGGACTAC | 10138 |
rs146490042 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42188032 | CTGTTATCTTAGTTG[C/T]ACCCTCAGGAGAAAC | 10138 |
rs146541434 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | YAF2 | GRCh38.p7 | 12:42198387 | TCAGGAGTTTGAGAC[C/T]AGCCTGAGCAACATG | 10138 |
rs146612716 | in-del | -/TTA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42183042 | CATAAAATGTTTTCG[-/TTA]TTATTATATCTGTTA | 10138 |
rs146621361 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | YAF2 | GRCh38.p7 | 12:42195082 | GTTCAGCGTGAGAAA[C/T]AAGAAACATACACAA | 10138 |
rs146720992 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42235373 | GTTTTTTTAACATTA[C/T]CAGAGAGGAAAAATA | 10138 |
rs146720997 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | YAF2 | GRCh38.p7 | 12:42184469 | CATGTGCCACCACGC[C/G]TGGCTAATTTTTATA | 10138 |
rs146789600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42172968 | GAAACAGGAAGTAGA[C/T]CTGTGGTTGCTCAGG | 10138 |
rs146831387 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42169383 | TAATGTTGAGGTTAC[G/T]TCATGCTGTTCTTAA | 10138 |
rs146913641 | in-del | -/T | 0.00636936 | 0.0560724 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42159003 | TATAATAAACACAAA[-/T]TTTAATTTTTCATTT | 10138 |
rs146921260 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42214775 | TTGGGAGGCTGAGGT[A/G]GGTGGATCACTTGAG | 10138 |
rs147027447 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | YAF2 | GRCh38.p7 | 12:42194438 | CACCTGAGGTCAGGA[A/G]TTCGAGACCAGTCTG | 10138 |
rs147037145 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42189171 | TCTCAAGAAGATGTA[C/T]AAAATTTCCAAATCT | 10138 |
rs147124780 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42176621 | AAAATAAGTCTAAAA[C/T]TGAATGCTTTCTTAC | 10138 |
rs147178600 | in-del | -/T | 0.0441095 | 0.141807 | intron-variant | YAF2 | GRCh38.p7 | 12:42203644 | CTAAATTTATCTAGA[-/T]TTTTTCCTAAATTTT | 10138 |
rs147185131 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | YAF2 | GRCh38.p7 | 12:42211781 | CAGCCAGGCACGGTG[G/T]CTTGCACCTGTGATT | 10138 |
rs147194331 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | YAF2 | GRCh38.p7 | 12:42208511 | TAATATTTAAGGGCT[A/T]AACTGTATCATTCAG | 10138 |
rs147301868 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42186243 | TCAGGCCTGTAATCC[C/T]AGAACTTTGGGAGGC | 10138 |
rs147398134 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | YAF2 | GRCh38.p7 | 12:42171269 | ATGCTGGGATTACAG[G/T]TGTGAGCCACCACAC | 10138 |
rs147494755 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | YAF2 | GRCh38.p7 | 12:42186010 | GTTCGAGACCAGCCT[A/G]ACCAACGTGGTGAAA | 10138 |
rs147504713 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232314 | AAAAGGCAAATAACA[G/T]CTTCAAATTATTATA | 10138 |
rs147514758 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | YAF2 | GRCh38.p7 | 12:42226861 | AGGAGGTCGCGGCGC[C/T]GGAGGCCCCAGAAGG | 10138 |
rs147558020 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | YAF2 | GRCh38.p7 | 12:42220093 | GGTTATGAGAAGGCC[C/T]TAAAATGGGAAAAAG | 10138 |
rs147617419 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160025 | AATAATTAGTAAAAC[A/G]TGTCAAAAACATTGG | 10138 |
rs147653032 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | YAF2 | GRCh38.p7 | 12:42203366 | TACTTTCATTTCTTT[C/T]AATATTTCTAGGGAG | 10138 |
rs147714635 | in-del | -/TTT | 0.0185938 | 0.0946107 | intron-variant | YAF2 | GRCh38.p7 | 12:42181890 | ACTGTTTTTTAACAG[-/TTT]TTTACATTTTACATT | 10138 |
rs147757573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42183261 | AAATTTGGCCAATCA[A/G]TAACTCAACAATGGT | 10138 |
rs147768205 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42178014 | ATAGGCTCCCTACCA[A/C]CCCCCTAATTGTAAA | 10138 |
rs147860507 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42165723 | TGATCTGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 10138 |
rs147870068 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42161415 | AGAAAAAAGCATCAT[C/T]ACATTTAAGCTTGTA | 10138 |
rs147969179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42224257 | AGCATAATTCATTGC[A/G]TATGTTTCCCAGTAA | 10138 |
rs147976580 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42170017 | CTGGTACCACAGGCA[C/T]GCATCACCACACCTG | 10138 |
rs147980606 | in-del | -/AAAA | 0.0352966 | 0.128072 | intron-variant | YAF2 | GRCh38.p7 | 12:42212149 | TTTAAATACTTGTAC[-/AAAA]GAAATACAGCAAATT | 10138 |
rs148031733 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | YAF2 | GRCh38.p7 | 12:42176195 | AGGTTGCAAGTGACA[A/G]AGTGTGACTCTGTCT | 10138 |
rs148042198 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42222607 | TGTTAAATTTATATA[A/T]ATTCAATACTTGAAA | 10138 |
rs148094275 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YAF2 | GRCh38.p7 | 12:42226166 | ATATATTTCTTAATA[C/T]GCTGTACACTTTCAC | 10138 |
rs148101627 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | YAF2 | GRCh38.p7 | 12:42162052 | AAATTATTTTAAATG[A/T]ATATCAAAAAAAATG | 10138 |
rs148155353 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | YAF2 | GRCh38.p7 | 12:42196027 | AGGAGTTGGAGACCA[C/G]CCTGGCCAACATGGT | 10138 |
rs148190662 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | YAF2 | GRCh38.p7 | 12:42211511 | GGAGGCCAAGGCAGG[C/T]GGATCACCTGAGGTT | 10138 |
rs148210738 | in-del | -/GGCCGCGGC | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238486 | GGGGGTGGCCGCGGT[-/GGCCGCGGC]TGCCTCGGGCGCCGG | 10138 |
rs148306848 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42185777 | ACAAACTACAGAATG[A/G]TGTAAACATAACTTT | 10138 |
rs148312018 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42198540 | GCAGTGAGCTGAGAT[C/T]GTACCACTGCACTCC | 10138 |
rs148534405 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | YAF2 | GRCh38.p7 | 12:42219562 | GAGAGATGCCCACAT[A/G]CTCACATTCCTGTAC | 10138 |
rs148620570 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | YAF2 | GRCh38.p7 | 12:42187234 | CAATCATAGTTCACT[A/G]TGACCTCAAACTCCT | 10138 |
rs148622140 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42229416 | TTATCAATAAAAAAA[A/T]AAATTAAAAAAAAAA | 10138 |
rs148629691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42202042 | TAAAAAAGTTTTTCA[C/T]GTGTATTATTTAATT | 10138 |
rs148716768 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | YAF2 | GRCh38.p7 | 12:42172637 | GAGTGAATAAATCAA[A/G]TACATACCCAAGAGA | 10138 |
rs148779586 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | YAF2 | GRCh38.p7 | 12:42223874 | ACACTGGGGCCTGTC[A/G]GGGGGTGGGGGGCAA | 10138 |
rs148854644 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42222262 | CCAACTCCTTGAATG[A/C]AAACTTGATATTCCA | 10138 |
rs148896169 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | YAF2 | GRCh38.p7 | 12:42197525 | CGCTGCACTAACTAC[A/G]TAGGGAAATGCCCAA | 10138 |
rs148898214 | in-del | -/CT | 0.0209421 | 0.100162 | intron-variant | YAF2 | GRCh38.p7 | 12:42208419 | CGATCGAGTGAGACT[-/CT]GTCTCACTTTATTTT | 10138 |
rs148947484 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | YAF2 | GRCh38.p7 | 12:42203968 | GCTGAGGAGGGAAAT[C/T]GCTTGAGGCCAGTTT | 10138 |
rs149062154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42179103 | TCCACCTTTAAGAAC[C/T]TGATTTACTTAGACT | 10138 |
rs149096959 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | YAF2 | GRCh38.p7 | 12:42193656 | GGACTACAGATGCAT[A/G]AACACCCAGCTAATT | 10138 |
rs149220319 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | YAF2 | GRCh38.p7 | 12:42214482 | TTGCCACGTTGCCCA[A/G]GCTGGTCTCGAACTC | 10138 |
rs149257518 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | YAF2 | GRCh38.p7 | 12:42164819 | TCACACCTGTAATCC[C/T]AGCACTTTGGGAGGC | 10138 |
rs149319478 | snp | A/C | 0.0532157 | 0.154195 | intron-variant | YAF2 | GRCh38.p7 | 12:42211876 | TAACATAGTGAAACC[A/C]CGTCTCTACTAAAAA | 10138 |
rs149538518 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | YAF2 | GRCh38.p7 | 12:42185667 | AGATTACAACTAGCT[A/G]AAAGCTCAGATGGTC | 10138 |
rs149542983 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | YAF2 | GRCh38.p7 | 12:42217896 | GAGCAATCATAAAGA[A/C]CATGAAATTGTGGAG | 10138 |
rs149627380 | snp | A/G/T | 0.000798403 | 0.0199641 | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42156957 | TTCAAAGTACAGTGC[A/G/T]GAAACTTCTACCAAT | 10138 |
rs149709260 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42196538 | TAGTGAGGGACCAGA[A/T]TATCTAGAACAAGAG | 10138 |
rs149761155 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | YAF2 | GRCh38.p7 | 12:42203733 | AATTTTTATGTCTGT[A/G]TTCATAAGTAAGACT | 10138 |
rs149848477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42174841 | AGAATATTTGTAAAA[A/G]TAACACTTAAGGAAA | 10138 |
rs149857245 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | YAF2 | GRCh38.p7 | 12:42186753 | GGAAGCAGATTAGTA[A/T]TAAATTTGCCAATGC | 10138 |
rs149867042 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234711 | AGACTTTAAAGGGGC[C/T]GAATGGTGGCTCATT | 10138 |
rs149918360 | snp | A/T | 0.00953873 | 0.0683987 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42158865 | TCCCTATTACATTTT[A/T]AAATTTTTACTATCT | 10138 |
rs150009186 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | YAF2 | GRCh38.p7 | 12:42209816 | AATTTTTTGTTTTTT[A/G]AGACAGAGTTTCGCT | 10138 |
rs150060440 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42213251 | CCTGAGGCCTGACAA[C/T]AGACATGTGAGTTAA | 10138 |
rs150121308 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42183837 | GACTTTCAGAGCTAG[A/C]GACGAAAAGTCAATG | 10138 |
rs150186170 | snp | G/T | 0.0193772 | 0.0965046 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238783 | AGCCCCCGCCTGCAG[G/T]ATACCGGGGGGAAGG | 10138 |
rs150237104 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42162788 | ATAGGAAACAGTATG[C/T]AAAGCAGATATCAGG | 10138 |
rs150322957 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42178420 | GGATCTGCCAGGTGA[A/G]GCAAATTATTACATT | 10138 |
rs150355908 | in-del | -/C | 0.0509478 | 0.151255 | intron-variant | YAF2 | GRCh38.p7 | 12:42168991 | AATATACTGAAGTCT[-/C]CTCCCATCTAGAAGG | 10138 |
rs150363723 | in-del | -/AATAT | 0.0162398 | 0.0886349 | intron-variant | YAF2 | GRCh38.p7 | 12:42224373 | TTAGGTGAAGAATAC[-/AATAT]ATTTCTTTTTTTTAT | 10138 |
rs150385208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42231147 | GGGTCATCTATCAAT[A/G]TTTACTATATTAGAA | 10138 |
rs150446620 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42199488 | TGGGACTCCAATTTA[C/T]CACCAAAAAATCCAC | 10138 |
rs150563414 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | YAF2 | GRCh38.p7 | 12:42176779 | CCAGCCTGGCCAATA[C/T]GGCGAAACCCCGTCA | 10138 |
rs150615285 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42182185 | AATATAAAAACATTA[A/T]AAAGAAGGTTTTTAA | 10138 |
rs150651400 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | YAF2 | GRCh38.p7 | 12:42226694 | AAATAATGCTAAAAC[A/G]ATTTATACCTACAAC | 10138 |
rs150705397 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233613 | AACTCTGGGGCTCAA[C/G]GGATCCTCCCACTTC | 10138 |
rs150712526 | in-del | -/TG | 0.0429648 | 0.14013 | intron-variant | YAF2 | GRCh38.p7 | 12:42201523 | GAATATTAAAGACAT[-/TG]TGTGTGTGTCTCCTC | 10138 |
rs150756283 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42158339 | GTGAAATCTATAAAA[C/T]ACTATTACTTTAGGT | 10138 |
rs150766395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42202282 | ATAATTTTTTTAACA[A/G]AGGTACTTACATAAA | 10138 |
rs150774454 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42216155 | GGGAAACAAAGTTAG[G/T]TACTAACATAATTTT | 10138 |
rs150831486 | in-del | -/A | 0.0252325 | 0.109451 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42230986 | CACTATAAAGGAAAT[-/A]AAAAAGAATACCTGC | 10138 |
rs150935737 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42183584 | AAACCAAAGCCTAAT[C/T]CACAGCAAGACCCTA | 10138 |
rs150945739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42229953 | GGGGTGGAGGGATGG[C/T]AATCCTAGAGGGCTT | 10138 |
rs151031387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42168705 | CACAGGAACAAGCCA[C/T]TGTTCTCAAAGTAGT | 10138 |
rs151083828 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42173654 | ACTACTCTAGCTTAA[C/G]CCAACAGACTTCTAC | 10138 |
rs151087769 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42204966 | TAGTAATTCTTGGCA[A/G]AACTCTGTAAAAATA | 10138 |
rs151093255 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42219706 | AATACCTCACACCCC[A/G]TCCACCTCATTATCT | 10138 |
rs151209657 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | YAF2 | GRCh38.p7 | 12:42194107 | CAAAAGAGTGAAAAC[A/G]TTAAAAAAATTAATA | 10138 |
rs151304821 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | YAF2 | GRCh38.p7 | 12:42177444 | ATGTTCTCACTGTGT[A/C]CTCACAAGGCCTTTC | 10138 |
rs180860452 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42172804 | AAATGAAATATTATT[A/T]CACCATAAAGAAGGA | 10138 |
rs180936260 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42178387 | GCAGTCAATGGCCTA[C/G/T]AAAACAAGATCAAAT | 10138 |
rs180953220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42217647 | ATTTTATCACTTATA[C/T]TTAATTACCACCAAA | 10138 |
rs180956937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42199283 | ACTATGTACACATGG[A/G]ACAGAATTTGACCAA | 10138 |
rs180969300 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157179 | AGGGAGCCCATCTGA[C/T]GAGGGCCTCATGCTG | 10138 |
rs180987849 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | YAF2 | GRCh38.p7 | 12:42169872 | CCTTTTCTCTCTCTC[C/T]CCTTTCTTTTTTTTT | 10138 |
rs181072023 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42211577 | CCCCATAACCCCATC[C/T]CTACTAAAAATACAA | 10138 |
rs181074429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42190543 | CCTTATCTTCACCAA[C/T]TACTTTTTCCAGCTT | 10138 |
rs181085114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42229796 | GTAACACCATGGTAA[A/G]TATTTGTATCTAAAC | 10138 |
rs181127654 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42158826 | CCTTTAAAGCATAGT[C/T]TTTGACTTAAAAATT | 10138 |
rs181134910 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42190108 | AGCACTTTGAGAGGC[A/T]AAGGCCAAAGGATTA | 10138 |
rs181137691 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42211055 | CACTAGATTTTGGTA[A/T]AGAAGCCACCATAGT | 10138 |
rs181141912 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | YAF2 | GRCh38.p7 | 12:42226862 | GGAGGTCGCGGCGCC[A/G]GAGGCCCCAGAAGGC | 10138 |
rs181152585 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42179825 | GAAATCAGTAGTATT[A/G]AAAGATGTTATTTGA | 10138 |
rs181187975 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | YAF2 | GRCh38.p7 | 12:42169238 | ATGACATTATTTAAC[A/G]TTCTCCTGCACCATA | 10138 |
rs181200530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42201188 | TCCAAATGAATATCC[A/G]TGTACATTCCTCCTT | 10138 |
rs181221415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42218334 | AATGATATGCAAGTA[C/T]ACATTTCCCTTTTTG | 10138 |
rs181282296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234093 | TGAGAATTGCTTGAA[C/T]CTGGGAGGTGGAGGT | 10138 |
rs181289932 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42223558 | GTACAGACAGGGTCT[C/T]GCTATGTTGCCCAGG | 10138 |
rs181310841 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | YAF2 | GRCh38.p7 | 12:42185423 | TAAAGAAGCAACAGG[A/G]CTTGAGAGGACTGGC | 10138 |
rs181318660 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42164956 | CGCCTGTAGGAGGCT[A/G]AGGTGGAAAAATCGC | 10138 |
rs181406433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42214982 | GCACTCCAGCCTGGG[C/T]AACAGAGTGAGACTC | 10138 |
rs181665263 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42236842 | GACAGATTAAGAATG[A/C]CACTGACTGAATTTC | 10138 |
rs181684037 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42164738 | ACTCTGGCTAACAAA[C/T]GCCCAAAAATCTAAC | 10138 |
rs181690154 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42185134 | AGTGGGCCAAGATCG[C/T]GCCACTGCACTCCAG | 10138 |
rs181743574 | snp | A/C/T | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42207684 | GATCACAAGGTCAGG[A/C/T]GATCAAGACCATCCT | 10138 |
rs181773427 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | YAF2 | GRCh38.p7 | 12:42173163 | AATGGCACAGTCATA[A/G]ACACTGCAGCCTCAA | 10138 |
rs181778254 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | YAF2 | GRCh38.p7 | 12:42193756 | TGATCTGCCTGCATC[A/G]GCCTCCCAAAATGCT | 10138 |
rs181781159 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42215306 | CTGGGTGCAATGGCT[A/C]ACACCTGTAATTCCA | 10138 |
rs181823112 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42235238 | CCAGTCTTGGCTTTA[A/G]TACTTGCCAACCTTA | 10138 |
rs181872699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42215804 | GATTGCACCTGTAGT[C/T]CTAGCTACTCGGGAG | 10138 |
rs181990949 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | YAF2 | GRCh38.p7 | 12:42182974 | AGCAAGGCTATTGGC[A/G]CCATTTTTCCAACAG | 10138 |
rs182161243 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157925 | ACACCCGGCCTATCT[A/T]CACTCTTACTTATAG | 10138 |
rs182161640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42200698 | AGAGGCAACCACTAT[C/T]ATAAGTGTGGGTAAA | 10138 |
rs182174394 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42223156 | ATTGACACCCGAGTT[G/T]TTTGAAAGAGGTTTA | 10138 |
rs182272546 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42162742 | AAAATATTGTACAAT[C/T]TAAGAATTAAAGCTG | 10138 |
rs182277123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42205880 | TTTGATACAACACTT[C/T]TGTTGTGATTTAGTT | 10138 |
rs182375342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42213560 | TTGTCTCAAGCCAAC[C/T]TGAGTGGCTCTAAGT | 10138 |
rs182399178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42217966 | AAAATGGCACAGTGG[C/T]CTAAAAAAGACCATG | 10138 |
rs182421907 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42178909 | AAATACCCCTTTAGC[C/T]AGGTGTGGTGGTGCG | 10138 |
rs182432501 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | YAF2 | GRCh38.p7 | 12:42171207 | ATATTGCCCAGGCTG[G/T]TCTCAACTCCTGACC | 10138 |
rs182450757 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42201871 | AGTTACCACACCCAG[A/C]CTGATGTCTTTTATT | 10138 |
rs182453950 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42230034 | GAGGCTGAGGCAGGC[A/G]GATCACGAGGTCAGG | 10138 |