SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs182459846 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42219699 | TGGGATGAATACCTC[A/G]CACCCCGTCCACCTC | 10138 |
rs182469380 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42159189 | AAACCACCAAATATC[A/G]CAACTGTTAGGGTCT | 10138 |
rs182479051 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42180853 | CTCAAGAGGCTGAGG[C/T]ATGAGAATCGCTTGA | 10138 |
rs182573337 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | YAF2 | GRCh38.p7 | 12:42225671 | TTTGTCAGGTTTGTC[A/G]AAGATTAGATGGTTG | 10138 |
rs182616106 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | YAF2 | GRCh38.p7 | 12:42209411 | TCTATAAAAAATAAA[A/C]AAATTAGTCAAGCAT | 10138 |
rs182649544 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42230434 | GCCTTGAACACTATC[C/G]TAAGGATCTCAGCCT | 10138 |
rs182696533 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | YAF2 | GRCh38.p7 | 12:42176278 | AGGAGTGCACCATCA[C/T]GCCAGCTAATTTTTG | 10138 |
rs182736228 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42224534 | CCTCCTCTAGCCCCC[C/G]ACCCCGCGACAGGCC | 10138 |
rs182934544 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42191492 | TAGGTGGGCTTTGTA[C/T]TTAATCTAATGTAAA | 10138 |
rs183012993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42191933 | TGTCTCTACTAAAAA[C/T]ACAAAAATTAGCCAG | 10138 |
rs183015284 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | YAF2 | GRCh38.p7 | 12:42186337 | CCAGCCTAGGTGACC[A/G]AGCAAAAACTCCAAC | 10138 |
rs183018519 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42196472 | TTAAAGAAGATGTCC[C/T]TTTGGCTATACCAGA | 10138 |
rs183056003 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | YAF2 | GRCh38.p7 | 12:42165864 | TTGTAAGTACTGATT[C/G]TTGGTTTTAAATTCT | 10138 |
rs183099967 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239192 | TCCAGCAACAGCCAT[C/G]TAACTGGTCTCCGAA | 10138 |
rs183195524 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YAF2 | GRCh38.p7 | 12:42171028 | GACAGAGTGAAACTC[C/T]GTCTCCCAGGCTGGA | 10138 |
rs183219186 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42212409 | GATACAGATATATTT[G/T]AATACCCTTTACCAT | 10138 |
rs183238280 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42191178 | AATGTTTAAAGTACT[A/C]CCATTACTGTCTCTC | 10138 |
rs183241246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42170539 | TTGTGGCCAGATGCG[A/G]TGGCTCACGCCTATA | 10138 |
rs183267009 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42211677 | TTGAACTCGGGAGGT[A/G]GAGGTCGCAATGAGC | 10138 |
rs183297135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42216384 | TGATGAAAGTAAAAG[C/T]CATTGGAGATGGCTA | 10138 |
rs183298743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42196702 | AATGAACAAAGTGTT[A/G]CTACATCTTTCTTTT | 10138 |
rs183306532 | snp | C/T | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239783 | GGAGGCCGAGGCGGG[C/T]GGATCACCTGAGGTC | 10138 |
rs183348651 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42229944 | TGATACCAAGGGGTG[G/T]AGGGATGGTAATCCT | 10138 |
rs183354930 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42216130 | GATATTACTAGATAA[C/T]TATATCCTTGGGAAA | 10138 |
rs183365699 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42187907 | CTCCTGGATCATTCA[C/G]TCTGGGGGAAGCCAG | 10138 |
rs183455804 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42221540 | CTCCGGCCTGGGTGA[C/G]AGAGCAAGACTCTAT | 10138 |
rs183487740 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | YAF2 | GRCh38.p7 | 12:42204834 | CCCAAAACACATGTT[A/G]TATAATTCCATTTTA | 10138 |
rs183618725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42174014 | TGCCACTGACCTCCT[C/T]TGTTTCCTGCTTAAA | 10138 |
rs183805415 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42186146 | CAGTGGCTGAGATTG[C/T]GCCACTGTACTCCAG | 10138 |
rs183813840 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42224367 | AATAATTTAGGTGAA[C/G]AATACAATATATTTC | 10138 |
rs183857383 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42195494 | AAAAGTATCTTGTAA[A/G]GGACAGTCCCCTAGT | 10138 |
rs183899914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42182068 | AACAAAGTAAGGTTT[C/T]ATAAAACAAGGGCAA | 10138 |
rs183907894 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42204202 | CTTTGTACACTGCTG[C/G]TGGGAAAATAAAATG | 10138 |
rs183908108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42220475 | AGAATGAAGCAATCA[C/T]AACATTTTAGAAGGT | 10138 |
rs183908743 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42160903 | AATAAATAATAAAAG[G/T]GGTAAAAGTAACAAA | 10138 |
rs183914901 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42165446 | CTACACCTCGAATGG[A/C]CAAAAGGTTTTTGTT | 10138 |
rs183937434 | snp | A/G | 0.00552802 | 0.0522824 | intron-variant | YAF2 | GRCh38.p7 | 12:42161787 | GCATGTTAAAAAGAA[A/G]GGTATTTTAAATTAC | 10138 |
rs183961294 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42202998 | GTTCCTCCTCATTCT[C/T]TTTCTTCTTCCAAAA | 10138 |
rs183987208 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42208250 | CTAACATGGTGAAAT[C/G]CTGTCTCTACTAAAT | 10138 |
rs184035675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42197733 | ATCTTAACATTTATA[C/T]AATCAGACTCCAAAT | 10138 |
rs184043166 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | YAF2 | GRCh38.p7 | 12:42177981 | TTTATCATCTGTTTT[A/C]CTCTACCAGAATAGA | 10138 |
rs184070634 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42156884 | GCTAAGAAGTCAAAG[C/T]GTTCTTTTACTATTA | 10138 |
rs184122722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42215028 | AATAAATAAATAAAT[A/G]AATGAATTCCATGAG | 10138 |
rs184127566 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42181329 | TTCTCCTACTGCTTT[C/T]CCTCTACTTCCTGCC | 10138 |
rs184130875 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42220313 | ATACTTTTATAATCA[C/T]GAGAAAAAGAATTAT | 10138 |
rs184134661 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42182520 | CATAAACTGAACTAC[A/C]ATATCATTGGAAAAG | 10138 |
rs184278541 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42162321 | GACCCTGGAGATCTG[A/C]CCAGTCTTTTGAGAC | 10138 |
rs184332060 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234939 | GCTGCAGTGAGCCTG[A/G]ATGATGCCACTGCAA | 10138 |
rs184357585 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42210266 | TATCCCAAGTAACTT[A/C]CTTTCTTTTCAATTA | 10138 |
rs184361918 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42226460 | TTGGCCCAGGAGTTC[A/G]AGACCAGACTGGGCA | 10138 |
rs184381383 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42189670 | TATAGATAAAACATA[C/T]AGTATATGCCTTTTT | 10138 |
rs184385727 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42168673 | TTTCTCCTTTAAAAA[A/C]ACAAGAACACTCCAT | 10138 |
rs184664779 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42217754 | GGAAGGAAACAAATA[A/T]AAAATATCTTCAATA | 10138 |
rs184685013 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42178434 | AAGCAAATTATTACA[C/T]TTCACCTTTGCTTTC | 10138 |
rs184706371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42199318 | TTAAATCCATCAAAC[A/G]TAATAATATACTTTG | 10138 |
rs184748070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42192626 | TTTTTAAAACACATA[C/T]GGAATTGGAGAGACT | 10138 |
rs184756325 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232569 | ATGGTTGCTAGAAAG[C/G]CTCCTCAGATAGACA | 10138 |
rs184806297 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42172490 | AATTTTATATAAGCC[A/T]ACATGAGACCTGAAT | 10138 |
rs184863696 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42166042 | TCCTACCTCAGCCTC[A/C]CGAGTAGCTGGGATT | 10138 |
rs184877914 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42214905 | GCTACTCAGGAGGCT[A/G]AGGCAGGAGAATCGT | 10138 |
rs184882746 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | YAF2 | GRCh38.p7 | 12:42193084 | TTTGGGTGGCCGAGG[G/T]GGGGCAGATCACTAG | 10138 |
rs184888780 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | YAF2 | GRCh38.p7 | 12:42172881 | TGCTAAGTGAAAAAC[A/G]CCAGTCATTAAAGAC | 10138 |
rs184955272 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42217403 | GGAGACAATTAACAT[C/G]CACTAACATATTCCA | 10138 |
rs184969410 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42192083 | AGATTTAAATAATAC[A/G]AAAAGTGTTATAGAA | 10138 |
rs184971042 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | YAF2 | GRCh38.p7 | 12:42214559 | TTACAGGTGTGAGCC[A/G]CCATGCCCGGCCTCC | 10138 |
rs184976598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42231574 | AAGTTTTCAGTGTTC[C/T]CTTAAAATCTGTTGG | 10138 |
rs185011124 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42171587 | AACTAAGCACTTGCC[C/T]ATGATTCTTACAGAC | 10138 |
rs185012782 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | YAF2 | GRCh38.p7 | 12:42217111 | AAGAAAGTAAGCATG[A/G]CACAAGAGAGAATAA | 10138 |
rs185109250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42197126 | TAGAACAAACTAGAG[C/T]GCAGAAAATACAAGT | 10138 |
rs185332407 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42177546 | AGGACTCCACTTTTA[A/C/T]GAGTTCATTTAATCT | 10138 |
rs185471874 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157219 | ATGGTGGAAAGCAGA[C/T]GGTGAACTGAGGAGG | 10138 |
rs185481883 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42189326 | TGGAGCCTGGGATTT[C/G]AATCAGAAAGAACAG | 10138 |
rs185538400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42226189 | ACTTTCACAGCTTCA[C/T]TGGTTTATTTTAGTC | 10138 |
rs185588972 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42167902 | AGCTACAGTCCAGGA[C/T]AGTCAAGTCATCGTC | 10138 |
rs185606466 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42163041 | AGAATCACCAAGAAG[G/T]CTTGTTTAGCTTGCT | 10138 |
rs185620564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42206566 | GTGAGCCGAGATAGC[A/G]CCACTGCACTCCAGC | 10138 |
rs185658013 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | YAF2 | GRCh38.p7 | 12:42207685 | ATCACAAGGTCAGGC[C/G]ATCAAGACCATCCTG | 10138 |
rs185667186 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42209828 | TTTGAGACAGAGTTT[C/T]GCTCTTGTTGCCCAG | 10138 |
rs185672533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42223235 | CTTCAAAGTTACATA[C/T]AGCGCCAGCATACTA | 10138 |
rs185683090 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42164890 | GCCTGGGCAACATAG[G/T]GAAAACCCATCTCTA | 10138 |
rs185720171 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42229986 | TTGAAAAGTACCATA[A/T]GGTGGCTTACGCCTG | 10138 |
rs185748545 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | YAF2 | GRCh38.p7 | 12:42191294 | ATTAGAAACTATACC[C/T]TAGATTATCAGTGTC | 10138 |
rs185758135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42183932 | TTTAAGGTGAAGCCA[A/G]TGCTCACTGACCATT | 10138 |
rs185767304 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42212003 | GCAGTGAGCCAAGAT[C/T]GTGCCTGGGAGACAC | 10138 |
rs185808192 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42218474 | AGTGGCCTATGAATT[G/T]TTGTTTTTATCTGTT | 10138 |
rs185821524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42222930 | TATAATTTATTGCTG[C/T]CAAATTCTTTTTTTT | 10138 |
rs185837619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42185698 | ATTTGAATTTTTTAG[C/T]TATATTTTAAATTAA | 10138 |
rs185844345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42180127 | CCACTAGTAATCCCT[A/G]CCTCCTGGTATTCAT | 10138 |
rs185908983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42165175 | AGACAAACATAGGCC[C/T]TGCCCTCATGCGCTA | 10138 |
rs185968985 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42208111 | AATAATAAATTTTTT[A/T]AAAAGAGCTGTATAT | 10138 |
rs186248837 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42170294 | AAGCTCAGAGCCTGA[C/T]AGGCATTCAACAAAT | 10138 |
rs186316759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42195818 | CCTAAGCAGATCCTA[C/T]GGGAGCACAGAAGGC | 10138 |
rs186381179 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42235446 | ACCCTGTTCCACACT[A/G]TTCTATACAAACACA | 10138 |
rs186404968 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42173470 | ATCATTAAATGACAC[A/G]ACAGTTTGGCATTTG | 10138 |
rs186406839 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42169313 | GTAAGTAGGTCCTTC[C/T]CAGTCATCTTATATC | 10138 |
rs186413024 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42193940 | CTAATGTATGTGTCT[A/G]TGTCTTCATTTTTAA | 10138 |
rs186414290 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42215367 | AGCCCAGGAGTTCGA[G/T]ACAAGCCTAGGCAAC | 10138 |
rs186481570 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42174514 | AGAGTACCTCAGGAC[C/T]GAGTCTTTGGATACC | 10138 |
rs186492426 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42211225 | TGAGATCAGGAGTTC[A/G]AGACCAACCTGGCCA | 10138 |
rs186559432 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | YAF2 | GRCh38.p7 | 12:42179196 | GCAGTGAGGCTGGGT[A/G]CATTGGCTCACACCT | 10138 |
rs186619482 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42218041 | AACTATGGCAAACAG[C/T]AAAAAATTCTGCTTT | 10138 |
rs186658093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42216146 | TATATCCTTGGGAAA[C/T]AAAGTTAGTTACTAA | 10138 |
rs186682142 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42196591 | AGACTAAATAAGTAA[C/T]AAAAAGGAATAAAGA | 10138 |
rs186682499 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | YAF2 | GRCh38.p7 | 12:42176563 | GTTTTTCCTCTCATA[C/T]TCACATCTAAGTCAC | 10138 |
rs186704130 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42190341 | AGAGTGAGTGCAACC[A/G]TCTCAAAAAAATAAA | 10138 |
rs186774119 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42158246 | AATCTCATAGTGCAC[A/G]CCCACCAGGTTCTTT | 10138 |
rs186782385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42200699 | GAGGCAACCACTATC[A/G]TAAGTGTGGGTAAAT | 10138 |
rs186790001 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238452 | CAGCACCCGCGGCGA[C/G]TTAGCCGGCGGGCGG | 10138 |
rs186816378 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42202110 | GATCTAGTTTCCCCC[C/G]CCATCTAGAAAACCA | 10138 |
rs186827558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42191945 | AAATACAAAAATTAG[C/T]CAGACGTGCTCACTT | 10138 |
rs186828747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42219928 | AACAACACATCTCCA[C/T]ATGATCTATATTATA | 10138 |
rs186830576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42171233 | TGACCTCAAGTGATC[C/T]GCCCACCTTGGCCTC | 10138 |
rs186996554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42215815 | TAGTCCTAGCTACTC[A/G]GGAGGCTGAGGCAGG | 10138 |
rs187116058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42162013 | GCTCAAACATTAGAA[C/T]ACTGTTACGTAAATC | 10138 |
rs187144313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42190696 | ATTTTTATTGTAATT[A/G]TTTTCTACTACAGTT | 10138 |
rs187158988 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42229835 | AGTAGAGTAAAAATA[C/T]AGTATCATTTTATGG | 10138 |
rs187174420 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | YAF2 | GRCh38.p7 | 12:42182300 | TAATGCTGATAGCAT[A/G]CAATGTAGAAGAGTT | 10138 |
rs187190012 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42221232 | GAAATCTTTAAGAAG[G/T]TACTTGCTAGCAAAT | 10138 |
rs187191644 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42204440 | TTATTCTCTAAGCAA[C/T]ACAATATAACAACTA | 10138 |
rs187326568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42208509 | GCTAATATTTAAGGG[C/T]TAAACTGTATCATTC | 10138 |
rs187358096 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42211669 | AGAATTGCTTGAACT[C/T]GGGAGGTGGAGGTCG | 10138 |
rs187368065 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42224685 | TTCCAGCTTCATCCA[C/T]GTCCCTGCAAAGGAC | 10138 |
rs187400000 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | YAF2 | GRCh38.p7 | 12:42186731 | ACTTTCCCACTAGGA[C/G]TAACCAGGAAGCAGA | 10138 |
rs187401450 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | YAF2 | GRCh38.p7 | 12:42165906 | TCTATCTATCTATCT[A/G]TCTATATCTATATCT | 10138 |
rs187476792 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232303 | CATCACAGTGAAAAA[A/G]GCAAATAACATCTTC | 10138 |
rs187494353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42188792 | TTCACTGTTGAGACG[C/T]TATTCACTTCAAAGC | 10138 |
rs187546351 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42225842 | GTTCTTTTTCCTTAG[A/G]ACTGTTTTGGGTATA | 10138 |
rs187594768 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42224428 | ACATGTGCAGAACCT[C/G]CAGGTTTGTTACATA | 10138 |
rs187608680 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42230999 | AATAAAAAGAATACC[C/T]GCTGAAGTAAAGCCA | 10138 |
rs187737911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42166625 | TTGAGAAAAATGAAC[A/G]AGGATATTGTCATCT | 10138 |
rs187739095 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239507 | GCTGTTTCTGTCCAT[C/T]TTTCTAGGTTTACAT | 10138 |
rs187745482 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | YAF2 | GRCh38.p7 | 12:42209762 | TTCCCTATATTGCTT[C/T]AGAACAACTAAACCA | 10138 |
rs187865469 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YAF2 | GRCh38.p7 | 12:42213844 | GTACAAACTCATTCT[C/T]TTTTATCTAATCTCA | 10138 |
rs187892712 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | YAF2 | GRCh38.p7 | 12:42165540 | GTGATCTCAGGTCAC[G/T]GCAAGCTCTGCCTCC | 10138 |
rs188021011 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157107 | GAGACTGGGCAATTT[A/G]TAAAGAAAACAGATT | 10138 |
rs188075453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42196949 | ACAGGAATGGAGAGT[C/T]ACTAAAGATTTAAGG | 10138 |
rs188079755 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | YAF2 | GRCh38.p7 | 12:42171080 | TAACTGCAACCTCCG[G/T]CTCCTGGGTTCAAGC | 10138 |
rs188082677 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | YAF2 | GRCh38.p7 | 12:42216706 | CCCTTTTCTCCTTCC[C/T]AAGCCTTACCCAACA | 10138 |
rs188088895 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239954 | GAGTGAGAGGTTGCT[C/G]TGAGCCGAGATCGTG | 10138 |
rs188089606 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42178024 | TACCACCCCCCTAAT[G/T]GTAAACAGGGACTTT | 10138 |
rs188099652 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42198910 | AGCACTTAAATGTGG[C/T]TAGTTCAAGTTAAGA | 10138 |
rs188099870 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42217599 | ATATTATTACAATTA[C/T]CATTATCATTAACTA | 10138 |
rs188154674 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, nc-transcript-variant, missense | YAF2 | GRCh38.p7 | 12:42212483 | TTTCATGATTCTTCA[C/T]TCTATGGAAACAAAG | 10138 |
rs188228509 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42221780 | AGAATCCTCCAAACT[C/T]AGCTGAAAATCCCAA | 10138 |
rs188232713 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | YAF2 | GRCh38.p7 | 12:42193594 | CTGCAGCTGCCTTGA[C/T]CTCCTGGGCTCAAGT | 10138 |
rs188233518 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42181546 | CTATACCAATAGTGG[C/G]CTCTGTCAGTCTATT | 10138 |
rs188236491 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42173058 | AGAGACAGAGAGAGA[G/T]AGAGGGAGAGAGAGA | 10138 |
rs188251064 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42220347 | AAGGAAAAAATAAAA[C/T]TCCATCCCCCACACC | 10138 |
rs188251335 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42215247 | TCAGCACTCCTAAAA[A/C]CTGAATCTTTAGGCA | 10138 |
rs188386369 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42191606 | TTTTTCCTTGTTTTC[C/T]TTCTTTTGCTATACA | 10138 |
rs188447692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42230053 | CACGAGGTCAGGAGA[C/T]GGAGACCATCCTGGC | 10138 |
rs188517759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42203438 | TTCTTTCTTTTTTGC[A/G]TATTGATAGAGATAT | 10138 |
rs188521225 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | YAF2 | GRCh38.p7 | 12:42223291 | TTTTACATCAATTAT[A/G]TAACTATCATCTTAA | 10138 |
rs188553062 | snp | A/C | | | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42161365 | AAAACAAAACAAAAC[A/C]AATCCAGACACAAAT | 10138 |
rs188668356 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42177804 | TTATTCTTTTTTTAC[A/T]GTATATGAATGCCAG | 10138 |
rs188672637 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | YAF2 | GRCh38.p7 | 12:42217114 | AAAGTAAGCATGACA[C/T]AAGAGAGAATAAAAT | 10138 |
rs188744818 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160425 | GTTTGGTAGGCATCA[C/T]TGCAATAAAATCTAA | 10138 |
rs188888354 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42176992 | ATAAATAACATCCCT[C/T]AATTGTTCTGCTACA | 10138 |
rs188946525 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42172072 | CTTCCAATGCTCTAT[A/G]CTCTTTCTATATTTG | 10138 |
rs188999359 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | YAF2 | GRCh38.p7 | 12:42163779 | TCTCTAGGAGCTAAA[C/G]AGCTTTCACTGAAGG | 10138 |
rs189006707 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42214685 | AATGATTTTTTTTTG[G/T]TATTTTTTTGTTTGC | 10138 |
rs189006896 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | YAF2 | GRCh38.p7 | 12:42192314 | GGAGATCAAGACCAG[C/T]CTGGGCAACACAGCA | 10138 |
rs189023441 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | YAF2 | GRCh38.p7 | 12:42181029 | GAGGATGGCTTCTTT[C/G]ATACACCTAGCTCTG | 10138 |
rs189081988 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42190495 | TGTTTTACTTAACTA[C/T]TTTTTCTGTTTTCTA | 10138 |
rs189089027 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42190094 | ACGTCTGTAATCCCA[A/G]CACTTTGAGAGGCTA | 10138 |
rs189096731 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | YAF2 | GRCh38.p7 | 12:42229501 | CCAAAGTGAATAAGA[C/T]GGTCTCTGCCCTGTA | 10138 |
rs189097524 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | YAF2 | GRCh38.p7 | 12:42168891 | GTTTAAAAACTCACA[A/G]TTACCTTTTAAAATG | 10138 |
rs189156570 | snp | C/T | 0.000144269 | 0.00849198 | intron-variant, missense, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42210615 | TAACTTCAAACAATG[C/T]GGATCTGTGGAGATT | 10138 |
rs189158576 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42226614 | GGCTGCAGTAAGCTA[A/T]ATCCACACCACTGCA | 10138 |
rs189162072 | snp | A/G | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42217924 | GAGGATGGGGAAGTA[A/G]AGGGCAGAAGAAACA | 10138 |
rs189167969 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42186170 | ACTCCAGCCTGGGCA[A/C]CAGAGCCAAACTCTG | 10138 |
rs189185939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42162561 | AAGGAAAGAGGCAGA[A/G]GGAAGGAGGGAAGAA | 10138 |
rs189188236 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | YAF2 | GRCh38.p7 | 12:42205372 | TTTCTTGCTGCTGCT[G/T]CTTCTCTTTTTTTTT | 10138 |
rs189221460 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42235173 | AAATCCCATCTGTGC[A/G]TCACACAAACAAATC | 10138 |
rs189373399 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | YAF2 | GRCh38.p7 | 12:42211469 | CATCCAGGCACAGTG[A/G]CTCACGCCTGTAATC | 10138 |
rs189393854 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42169320 | GGTCCTTCTCAGTCA[C/T]CTTATATCTAAACTG | 10138 |
rs189461908 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42182737 | TATTGAATTTTCCAT[C/T]TTAATATAAACTGGC | 10138 |
rs189630298 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | YAF2 | GRCh38.p7 | 12:42167913 | AGGACAGTCAAGTCA[C/T]CGTCTGGCTTTGTTT | 10138 |
rs189638322 | snp | C/G/T | 0.00438332 | 0.0466095 | intron-variant | YAF2 | GRCh38.p7 | 12:42189387 | TAGGATTTTTTAATG[C/G/T]TACTCTGTTTTTGCA | 10138 |
rs189751990 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42159159 | TAATTAAACAGAAAA[C/T]TACATTACCACATGA | 10138 |
rs189757623 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42214920 | AAGGCAGGAGAATCG[C/T]TTGAACCTGGGAGGC | 10138 |
rs189761621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42180818 | CTGGATGTGGTGGTG[C/T]GTGCCTATAATCCCA | 10138 |
rs189786867 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42172719 | ATTATCCTTAACAGC[A/C]CCAAAGCGGAAGCAA | 10138 |
rs189830512 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | YAF2 | GRCh38.p7 | 12:42218691 | TATGACTGGCTCCCA[A/G]AATAATCTTATTAAA | 10138 |
rs189832448 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42201592 | TCTTTTTTGTTGCTG[C/T]TGCTGTTGTTGTTGT | 10138 |
rs189934621 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | YAF2 | GRCh38.p7 | 12:42184413 | CTCCCAGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 10138 |
rs189980020 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42196668 | GCAAAAGCCCCAACT[A/G]AATGGTGCAAACTGT | 10138 |
rs189980201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42216285 | AAAGTATTATCTTGT[C/T]ACAACTTAAAAATAC | 10138 |
rs189986342 | snp | C/T | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239610 | TCTCAGCCTGCTTCT[C/T]CTGTTTCTTAGCTGA | 10138 |
rs189994096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42192843 | ATATAGTCACACGTC[A/G]CATAACAACATTTTG | 10138 |
rs190014648 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233596 | AGCTCACTGCAACCT[C/G]GAACTCTGGGGCTCA | 10138 |
rs190149832 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42207675 | AGGCGGGCAGATCAC[A/G]AGGTCAGGCGATCAA | 10138 |
rs190410618 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42185268 | CAATCTCATGACCAA[C/G]CTTTCACAGATGAGG | 10138 |
rs190415265 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | YAF2 | GRCh38.p7 | 12:42164941 | GCCAGTAAAGGTACG[C/T]GCCTGTAGGAGGCTG | 10138 |
rs190415736 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42165843 | CTAATCCTATGAACA[G/T]TCATCTTGTAAGTAC | 10138 |
rs190420974 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | YAF2 | GRCh38.p7 | 12:42193962 | CATTTTTAACAAACA[C/G]TTTAAAAAGTAATAA | 10138 |
rs190476754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42186235 | TTGGTGGCTCAGGCC[C/T]GTAATCCCAGAACTT | 10138 |
rs190480968 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | YAF2 | GRCh38.p7 | 12:42215722 | GAGGTCAGGAGTTCA[A/G]GACAGCCTGGCCAAC | 10138 |
rs190486944 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42236234 | TAAACCAACTCCAAC[C/T]TTACACAGCCAAGAA | 10138 |
rs190537951 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42210052 | ATCCACCCGCCTTGG[C/T]CTCCAAAAGTACTGG | 10138 |
rs190541666 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | YAF2 | GRCh38.p7 | 12:42178505 | CTACTCTAGTATTAT[C/T]GTCATCTCTCCCCTC | 10138 |
rs190568390 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42191308 | CCTAGATTATCAGTG[C/T]CTCTTTTTCTCACCT | 10138 |
rs190570415 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42212201 | TGCCTAAAAATGGCC[A/G]TCACTGAAATAAAAA | 10138 |
rs190632265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42229992 | AGTACCATATGGTGG[C/T]TTACGCCTGCAATCA | 10138 |
rs190719233 | snp | A/G | 0.00517822 | 0.0506191 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42158620 | AGGATTCAAACATGA[A/G]GTGTCAGTTAGCACG | 10138 |
rs190723848 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | YAF2 | GRCh38.p7 | 12:42190959 | ACTTAACAATGTTTA[A/C]AAATATAACCTATTT | 10138 |
rs190730094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42170409 | TGCTCATTTATCTTG[C/T]GTATCTTAATGATAA | 10138 |
rs190735961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42211670 | GAATTGCTTGAACTC[A/G]GGAGGTGGAGGTCGC | 10138 |
rs190794037 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42226287 | TAAGTGGCCACAAAT[A/G]AGATCATAACAATAT | 10138 |
rs190796121 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157315 | CATTCCTGCAAGAGC[A/G]AATCCATTCCAGAAC | 10138 |
rs190809846 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42200422 | GCACCTAGTGCTTAT[A/C]TGCTGCTCCACTACA | 10138 |
rs190838062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42208194 | ACACTTTGGGAGGCC[A/G]AGGCGGGCAGATCAC | 10138 |
rs190876871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42165241 | AGAAAACAGGAGGAG[A/G]AGTTATTATAGACAG | 10138 |
rs190978931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42216025 | TTGACACCAACAAGT[A/G]CCCAATGTTTTGGGA | 10138 |
rs191009569 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | YAF2 | GRCh38.p7 | 12:42175350 | GTAGTTGCCTAGCAA[A/C]CAGAGATGGGATGGG | 10138 |
rs191088960 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42185723 | AATTAAGGTATATAC[A/C]TTGTTGTTTTTGGAT | 10138 |
rs191103282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42223815 | TCACTCATAAGTGGG[A/G]GTTGAACAATGAGAA | 10138 |
rs191233331 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42182343 | TGGTAACAGGTATTT[C/T]TGCTTTACAGTTGGA | 10138 |
rs191241364 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | YAF2 | GRCh38.p7 | 12:42162254 | TCACTCCTTATTGCT[C/T]AAATCCTTTAAGTTT | 10138 |
rs191242095 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238928 | AGACTCAAGAGAGAT[A/T]AGGTGACTTCCTCTA | 10138 |
rs191255763 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42204460 | TATAACAACTATTTA[C/T]ATAGCACTTGGGTTA | 10138 |
rs191484567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42187517 | GTGCTTCTATATTCT[C/T]TGTGTTCCAAGAATA | 10138 |
rs191486417 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | YAF2 | GRCh38.p7 | 12:42166021 | CCTCCTAGCTTCAAG[C/T]GATTCTCCTACCTCA | 10138 |
rs191497618 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42176727 | AGCACTTTGGGAGGC[A/T]GAGGTGGGTGGATCA | 10138 |
rs191502815 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42208974 | TTTATATTTAAAATG[C/G]CTTTTTAGAAATAGA | 10138 |
rs191553580 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | YAF2 | GRCh38.p7 | 12:42225632 | CCATTTATTAAATAG[C/G]GAATCCTTTCCCCAG | 10138 |
rs191574456 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | YAF2 | GRCh38.p7 | 12:42224512 | AGGCAATTCTTCTAA[C/T]GCTATCCCTCCTCTA | 10138 |
rs191682981 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | YAF2 | GRCh38.p7 | 12:42201128 | TAACTATTCTATATC[G/T]TATTTATCCATGCCT | 10138 |
rs191710336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42221462 | TGTAGTCCTAGCTAC[C/T]TGGGAGGTTGAGCTT | 10138 |
rs191737571 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42173773 | AATATTCCAATTACT[A/G]TTCTAAGTACTGGGA | 10138 |
rs191803376 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | YAF2 | GRCh38.p7 | 12:42220110 | AAAATGGGAAAAAGT[C/T]TACTTTTTTCCCATT | 10138 |
rs191826633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42181236 | CTGTGCTAGTTGGTG[C/T]TTCACTTCTTTGTGA | 10138 |
rs191834635 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | YAF2 | GRCh38.p7 | 12:42208835 | AAGAACAAACAAAAG[C/T]TTCAAACTGAAGAAA | 10138 |
rs191940205 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42218227 | ACACACACACACACA[C/G]AGATGATTATCGATC | 10138 |
rs191973680 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | YAF2 | GRCh38.p7 | 12:42179650 | AAAAATGAGCCAGGC[A/G]TGGTGGCACGTGCCA | 10138 |
rs192089607 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | YAF2 | GRCh38.p7 | 12:42202875 | CTCCTGACCTAAGGT[A/G]ATTCACCCGCCTCCG | 10138 |
rs192092044 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42229857 | ATTTTATGGGACTGT[A/G]TATGTGGTCCCCCAC | 10138 |
rs192112404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42167938 | TTGTTTCCATACCTC[A/G]AGCTCTGACTGCATC | 10138 |
rs192122703 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | YAF2 | GRCh38.p7 | 12:42189660 | ATACATACATTATAG[A/G]TAAAACATATAGTAT | 10138 |
rs192123064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42216859 | AACTAACACCACTCA[C/T]TCAACTGCTTAAGCC | 10138 |
rs192126949 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42240240 | AATCCATCGTAAAGT[A/T]GAAAAATCGTAAGTC | 10138 |
rs192135706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42160880 | CTCTACCAAATTTCT[A/G]AGCATATAATAAATA | 10138 |
rs192160594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42161476 | ATCTTTCAAACTCAG[C/T]AAAACCTTTCCTGAT | 10138 |
rs192235505 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42181708 | ATGAAAATAATTCAC[A/G]GATGCCAGAATTCAA | 10138 |
rs192267114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42214883 | GTGGCAGGCGCCTGC[A/G]GTCCCAGCTACTCAG | 10138 |
rs192275824 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42230171 | CTGAGGCAGGAGAAT[C/T]GCTCAAATCTGGGAG | 10138 |
rs192284267 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232471 | AATTTACCCATATAC[A/C]ATTAACCAGTGTGAG | 10138 |
rs192319937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42191813 | AAAGATTTGGCCATG[C/T]ACAGTGGCTCATGCC | 10138 |
rs192362642 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42191968 | GCTCACTTGAACCCA[A/G]GAGGAGGAGGCTGCA | 10138 |
rs192366390 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42171440 | GGCTGCAGTGCACTA[C/T]GATCATACCTCTGAA | 10138 |
rs192425974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42209820 | TTTTGTTTTTTGAGA[C/T]AGAGTTTCGCTCTTG | 10138 |
rs192428795 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42214236 | CTAACCAAAGGGCTT[G/T]CAACTTGCCGTTAAC | 10138 |
rs192431083 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42231277 | AAAACAAAGATATTT[C/T]GTATGAAGAGTGGCA | 10138 |
rs192447071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42166720 | CACTATCACTGGCTT[C/T]ACACCATCCCCTGAT | 10138 |
rs192540690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42210133 | AGAAGCAGCTATTAC[A/G]TAAATAAGATACTTT | 10138 |
rs192552022 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42226387 | TGCTAAAACATCTGG[G/T]TGCAGTGGTTCATGC | 10138 |
rs192604086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42177919 | ACTATGCTTTATTTT[C/T]TTCAAAGCACTTCTC | 10138 |
rs192623142 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42217277 | TTTTATAAGAAAATG[G/T]TTTTATTCCTAATTT | 10138 |
rs192678968 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | YAF2 | GRCh38.p7 | 12:42213544 | ACATCGCAAATTTCA[A/G]TTGTCTCAAGCCAAC | 10138 |
rs192704466 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42171165 | ACCTGGCTAATTTTG[C/T]ATTTTTAGTAGAGAC | 10138 |
rs192771227 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42225965 | CTATAAATTACTTTG[C/G]GAAGTATGGCCATTT | 10138 |
rs192788946 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42189217 | CTAGTAAATAATCAA[C/G]TACAACTGCATACTC | 10138 |
rs192853453 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42197511 | AAGTAACAGCTAAAC[A/G]CTGCACTAACTACGT | 10138 |
rs192884716 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42197112 | GTCATGACAACAGAT[A/G]GAACAAACTAGAGCG | 10138 |
rs192955730 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42165076 | CAAAAAAAAAAAAAA[A/G]AAAGAAAAGAAACTA | 10138 |
rs192972737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42172423 | AGCCTTCTTAAATAT[A/G]CTTCAGCTGAGGCAT | 10138 |
rs192974632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42203587 | GTGTAAGAGTGGTTT[C/T]TTAAAACTTTAATGG | 10138 |
rs193032649 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42222776 | TTTCCTTTTCTTTCA[A/G]AAGCATTGTTGAGAA | 10138 |
rs193152756 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | YAF2 | GRCh38.p7 | 12:42177484 | TGCACAGGGAGAGAC[C/T]GACAAACCTCTCCCT | 10138 |
rs193182095 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | YAF2 | GRCh38.p7 | 12:42192475 | GATCGTGCCACTGCA[C/G]TCTAGCCTGGGCAAC | 10138 |
rs193191501 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42220458 | AACTGTTGGTGAAGT[A/C]AAGAATGAAGCAATC | 10138 |
rs199502778 | in-del | -/T | 0.0501905 | 0.150254 | intron-variant | YAF2 | GRCh38.p7 | 12:42222754 | CATGATATTCAGGGA[-/T]TTTTTTTTTCCTTTT | 10138 |
rs199532044 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157692 | GAAAGCATTTAATAA[A/C]AATAAAACCTTTATT | 10138 |
rs199574153 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42167187 | GACAAATACCTAATG[C/T]ATGCGGGGTTTAAAA | 10138 |
rs199579017 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42173933 | TAGTCTGACTTCCCT[A/G]CCCTTACTCTTAATT | 10138 |
rs199609133 | snp | A/G | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234207 | GAGAAAAGAAAAGAA[A/G]AGAAAAGAAAAGAAA | 10138 |
rs199649871 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42215963 | AAATAAATAAATAAA[G/T]AAATAAATAAATAAA | 10138 |
rs199662584 | in-del | -/A | | | intron-variant | YAF2 | GRCh38.p7 | 12:42198116 | TGGGCCTCACCTTAT[-/A]AAAAAAAAAGTCATC | 10138 |
rs199729054 | in-del | -/TAGTATTCCA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42224727 | CTTTTTACAGCTGCA[-/TAGTATTCCA]TGGTGTATATGTGCC | 10138 |
rs199740546 | snp | A/G | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234194 | TCAAAAAAAAAAAGA[A/G]AAAAGAAAAGAAAAG | 10138 |
rs199777290 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42207475 | GATAAATTATTAATA[A/T]TATTATACTAAATAA | 10138 |
rs199858576 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42206867 | ACACTTTCTCCTCAT[C/T]TTTTTTTAAAATTTC | 10138 |
rs199878593 | in-del | -/CTTA | 0.0154538 | 0.0865337 | intron-variant | YAF2 | GRCh38.p7 | 12:42212739 | GATCTGTGATAGATT[-/CTTA]CTTAAATTTAAGATA | 10138 |
rs199884904 | in-del | -/A | 0.0103295 | 0.0711199 | intron-variant | YAF2 | GRCh38.p7 | 12:42189206 | AGAAAACCTGCTAGT[-/A]AAATAATCAACTACA | 10138 |
rs199914392 | snp | G/T | | | missense, nc-transcript-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42161639 | ATGGCTATTCTTTTT[G/T]CTAGTTGTTTCCTTT | 10138 |
rs199967223 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42213066 | ATGTCATTAAGAGCC[A/C]GGCACGGTGGCTCAA | 10138 |
rs200044747 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42170695 | ACACACACACACACA[A/C]ATTAGCTGGGCATGG | 10138 |
rs200136942 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42212705 | GTTAGGTTGACAACA[C/T]ACCTGTCAAGATTGT | 10138 |
rs200164207 | snp | A/C | 0.00200143 | 0.0315707 | intron-variant, missense, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42210609 | TCACAATAACTTCAA[A/C]CAATGTGGATCTGTG | 10138 |
rs200234774 | in-del | -/ACAC | | | intron-variant | YAF2 | GRCh38.p7 | 12:42223332 | TTCTTTAAAATACAT[-/ACAC]ACACACACACACACA | 10138 |
rs200260045 | in-del | -/TTAAA | 0.0217236 | 0.101931 | intron-variant | YAF2 | GRCh38.p7 | 12:42225886 | GGTTCCACATGAAAT[-/TTAAA]TTAGTTTTTCTAATT | 10138 |
rs200330208 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157363 | AAAGCCTTTAATCCA[C/T]CTCAATGACCTAATC | 10138 |
rs200411659 | in-del | -/A | | | intron-variant | YAF2 | GRCh38.p7 | 12:42174101 | TCATACCTCAAAAAG[-/A]AAAAAAAAAAAAAAA | 10138 |
rs200439535 | in-del | -/AAATAAATAAATAAAT | | | intron-variant | YAF2 | GRCh38.p7 | 12:42215928 | AGATTCCAGCTCAAA[-/AAATAAATAAATAAAT]AAATAAATAAATAAA | 10138 |
rs200457903 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42206862 | TTAAAACACTTTCTC[A/C]TCATCTTTTTTTAAA | 10138 |
rs200458651 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42205619 | ACCTCATGATCCACC[C/T]GCCTCGGCCTCCCAA | 10138 |
rs200487041 | snp | C/T | 0.000111528 | 0.00746671 | intron-variant | YAF2 | GRCh38.p7 | 12:42160875 | TTTCCCTCTACCAAA[C/T]TTCTGAGCATATAAT | 10138 |
rs200496908 | in-del | -/TCTTC | 0.0310518 | 0.120672 | intron-variant | YAF2 | GRCh38.p7 | 12:42205372 | TTTCTTGCTGCTGCT[-/TCTTC]TCTTTTTTTTTTTTT | 10138 |
rs200510317 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42224856 | GTGCATGTGTCTTTA[C/T]AGTAGAATGATTTAT | 10138 |
rs200515043 | in-del | -/ACAC | | | intron-variant | YAF2 | GRCh38.p7 | 12:42218186 | TCAGGCTACTAGGAA[-/ACAC]ACACACACACACACA | 10138 |
rs200563675 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42229419 | TCAATAAAAAAATAA[A/T]TTAAAAAAAAAAAAA | 10138 |
rs200572183 | snp | A/G | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234229 | GAAAAGAAAAGAAAA[A/G]AAAGAAAAGAAACTT | 10138 |
rs200657939 | in-del | -/A | | | intron-variant | YAF2 | GRCh38.p7 | 12:42205056 | AATAAAGTTGTTATT[-/A]AAAAAAAAAAAACCA | 10138 |
rs200750133 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42215964 | AATAAATAAATAAAT[A/C]AATAAATAAATAAAG | 10138 |
rs200823717 | in-del | -/AGAAAAGAAA | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234193 | CTCAAAAAAAAAAAG[-/AGAAAAGAAA]AGAAAAGAAAAGAAA | 10138 |
rs200835905 | snp | A/G | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234197 | AAAAAAAAAAGAGAA[A/G]AGAAAAGAAAAGAAA | 10138 |
rs200874701 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42192344 | AAGACCTCATCTCCA[C/T]ACACACACACAAAAA | 10138 |
rs200894773 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | YAF2 | GRCh38.p7 | 12:42223357 | ACACACACACACACA[A/G]ATATATACACACAAA | 10138 |
rs200906149 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42196354 | GCAAATATGGCTGGG[A/G]CATGACTTTATACAG | 10138 |
rs200919169 | in-del | -/T | | | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42157074 | CACTTTTTTTTTTTT[-/T]GCTATAACAGAATAC | 10138 |
rs200972161 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42227490 | GCGCCTCTGCCCCGC[C/T]GCCCCATCTGGGATG | 10138 |
rs200972190 | in-del | -/AT | | | intron-variant | YAF2 | GRCh38.p7 | 12:42223330 | GTTTCTTTAAAATAC[-/AT]ACACACACACACACA | 10138 |
rs201042767 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42229421 | AATAAAAAAATAAAT[A/T]AAAAAAAAAAAAAAA | 10138 |
rs201123435 | snp | C/T | | | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42157063 | AGTATCTCAATCCAC[C/T]TTTTTTTTTTTGCTA | 10138 |
rs201152987 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42207472 | CAAGATAAATTATTA[A/T]TAATATTATACTAAA | 10138 |
rs201194749 | snp | A/G | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232775 | GATAGTTGGTTTAAG[A/G]TTCTTTCAGAATGTG | 10138 |
rs201251505 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42210105 | GCCCGGCCAACTAAA[-/T]GTATAATTTTTTAGA | 10138 |
rs201327216 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42227760 | GGTGGGGGGGTCAGC[C/T]CCCCGCCTGGCCAGC | 10138 |
rs201337155 | in-del | -/AAC | 0.030665 | 0.119967 | intron-variant | YAF2 | GRCh38.p7 | 12:42229435 | TTAAAAAAAAAAAAA[-/AAC]ATTTAAATATCTACA | 10138 |
rs201340047 | in-del | -/A | | | intron-variant | YAF2 | GRCh38.p7 | 12:42221561 | AGACTCTATCTCTTT[-/A]AAAAAAAATTTTTTT | 10138 |
rs201366865 | in-del | -/AAGAG | 0.00318978 | 0.0398085 | intron-variant | YAF2 | GRCh38.p7 | 12:42230275 | AAAAGAAAGAGAAGA[-/AAGAG]AAGAGAAGAAAGAGA | 10138 |
rs201386007 | snp | A/G | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234192 | CCTCAAAAAAAAAAA[A/G]AGAAAAGAAAAGAAA | 10138 |
rs201420657 | in-del | -/ACACACAC | | | intron-variant | YAF2 | GRCh38.p7 | 12:42218186 | TCAGGCTACTAGGAA[-/ACACACAC]ACACACACACACACA | 10138 |
rs201509095 | in-del | -/AGAAA | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234193 | CTCAAAAAAAAAAAG[-/AGAAA]AGAAAAGAAAAGAAA | 10138 |
rs201516212 | in-del | -/A | 0.02016 | 0.0983543 | intron-variant | YAF2 | GRCh38.p7 | 12:42203545 | AGCCTTTACTGTAAG[-/A]AAAAAAAAAGCTCAT | 10138 |
rs201560900 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42174159 | AGCCACTGCCCCATT[A/T]GTTTTCTTTTCCATG | 10138 |
rs201603450 | in-del | -/TTT | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42191374 | TATGAATCCACTGAC[-/TTT]TTTTTTTTTGCTTAT | 10138 |
rs201699421 | in-del | -/GGTAGGTACAGGA | 0.0170251 | 0.090679 | intron-variant | YAF2 | GRCh38.p7 | 12:42175366 | CAGAGATGGGATGGG[-/GGTAGGTACAGGA]GGGAGGAATTAAAAA | 10138 |
rs201734364 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42206865 | AAACACTTTCTCCTC[A/T]TCTTTTTTTAAAATT | 10138 |
rs201747899 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42183857 | AAAAGTCAATGCCTT[C/G]ATTCAAAGCTTCAAA | 10138 |
rs201752166 | in-del | -/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42166913 | TGATAAAACACTGGA[-/T]TTTTTTTTTCAAAAT | 10138 |
rs201809207 | snp | A/G | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234204 | AAAGAGAAAAGAAAA[A/G]AAAAGAAAAGAAAAG | 10138 |
rs201862365 | in-del | -/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42188690 | AGTGCCCAGTCAGAA[-/T]TTTTTTTTTTAATTT | 10138 |
rs201912476 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157451 | GAGTTTTGGTGAGGA[A/C]AAACCATATCCAAAC | 10138 |
rs202017919 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42213064 | AGATGTCATTAAGAG[C/G]CAGGCACGGTGGCTC | 10138 |
rs202063932 | in-del | -/CTC | 0.0376037 | 0.131863 | intron-variant | YAF2 | GRCh38.p7 | 12:42206859 | TCTTTAAAACACTTT[-/CTC]CTCATCTTTTTTTAA | 10138 |
rs202080688 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42222952 | CTTTTTTTTTTTTTT[A/C]TTACCATTGGTAGTT | 10138 |
rs202108934 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42236986 | CATTTGTCTAAGAGA[C/T]TGCCATTTAATCAAA | 10138 |
rs202147527 | snp | A/C/G | 5.75809e-05 | 0.00536542 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42237711 | CCGAGGACGGCTTCG[A/C/G]CTGCCGCTTCGGCCT | 10138 |
rs202166970 | snp | A/G | 0.00695257 | 0.0585487 | intron-variant, synonymous-codon, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42237643 | CATCATGCACTTGAA[A/G]GCCTCGGCGCTGTTC | 10138 |
rs202195796 | in-del | -/T | 0.0517044 | 0.152246 | intron-variant | YAF2 | GRCh38.p7 | 12:42224382 | AATACAATATATTTC[-/T]TTTTTTTTATTATAC | 10138 |
rs202240022 | in-del | -/AAATAAAT | | | intron-variant | YAF2 | GRCh38.p7 | 12:42215928 | AGATTCCAGCTCAAA[-/AAATAAAT]AAATAAATAAATAAA | 10138 |
rs367571610 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42213888 | GGTACTACACAGACC[G/T]CCATTTCTAATTGGA | 10138 |
rs367581231 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42225340 | GATGATAGTTTCTTT[C/T]GCTGTGCAGAAGCTC | 10138 |
rs367595890 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42197141 | CGCAGAAAATACAAG[A/T]AAGAAAATTATTACA | 10138 |
rs367706327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42225006 | CAACAGTGTAAAAGC[A/G]TTCCTATTTCTCCAC | 10138 |
rs367707566 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42170993 | AGGAATTGTTTAGTT[C/T]TTTTTTGTTTTTGTT | 10138 |
rs367720351 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42215371 | CAGGAGTTCGAGACA[A/C]GCCTAGGCAACACAG | 10138 |
rs367725716 | snp | C/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42235224 | TGCTCTGCAGCTATC[C/T]AGTCTTGGCTTTAGT | 10138 |
rs367782777 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42206335 | GACGTCTGGCTGGGC[A/G]CAGTGGCTCACGCCT | 10138 |
rs367820744 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42187769 | CTCACATCTCTTGCA[C/T]TCATGCCTTTGGCCT | 10138 |
rs367875884 | snp | A/C | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232275 | GCAGTTTTACCCATC[A/C]CTGCCTCTGCACCAT | 10138 |
rs367982598 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42165154 | TAAGGAGATTAACCA[C/T]GAACAAGACAAACAT | 10138 |
rs368104608 | snp | A/G | | | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42156899 | CGTTCTTTTACTATT[A/G]TTTTCCTTACATACG | 10138 |
rs368113008 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42180783 | GCAGAACCCCATCTC[C/T]ACTAAAATAGAAAAA | 10138 |
rs368117651 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42204639 | GAAGACTATTCATAA[C/T]AATCAAAAAGTGCAA | 10138 |
rs368133025 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42204201 | CCTTTGTACACTGCT[A/G]GTGGGAAAATAAAAT | 10138 |
rs368152030 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42169936 | AGTGCAGTGGTACAA[A/T]CACAACTCACTACAG | 10138 |
rs368165778 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42214865 | GGAAATTAACCAGGC[A/G]TGGTGGCAGGCGCCT | 10138 |
rs368203178 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42214812 | AGTTCGAGACCAGCC[A/G]GGCCAACACGGCGAA | 10138 |
rs368203482 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42183643 | GAGGTGAGGAAGCTG[A/C]AGAAAAGTCAAGCCA | 10138 |
rs368208976 | snp | A/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232522 | CAAACAAGTAAGAAA[A/T]CTCCTAGAATAAGGA | 10138 |
rs368238479 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42202884 | TAAGGTGATTCACCC[A/G]CCTCCGCCTCTCAAA | 10138 |
rs368282782 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42226105 | CACATCCCTTGTAAG[G/T]TGTATTCCTAGGTAT | 10138 |
rs368285185 | snp | C/T | | | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42210132 | TAGAAGCAGCTATTA[C/T]GTAAATAAGATACTT | 10138 |
rs368289685 | snp | C/T | 0.0788843 | 0.182262 | intron-variant | YAF2 | GRCh38.p7 | 12:42227988 | GGGGGGTCAGCCCCC[C/T]GCCTGGCCAGCCGCC | 10138 |
rs368412248 | in-del | -/CA | 0.0126979 | 0.078662 | intron-variant | YAF2 | GRCh38.p7 | 12:42192341 | GCAAGACCTCATCTC[-/CA]CACACACACACACAA | 10138 |
rs368434842 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42225917 | AATTCTGTGAAGAAA[C/G]TCAATGGTAGCTTGA | 10138 |
rs368459059 | snp | C/T | | | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42210077 | TACTGGGATTACAAG[C/T]GTGAGTCAGCAAGCC | 10138 |
rs368462084 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant | YAF2 | GRCh38.p7 | 12:42202105 | GCAGAGATCTAGTTT[-/C]CCCCCCCATCTAGAA | 10138 |
rs368620433 | in-del | -/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42170999 | TCAGGAATTGTTTAG[-/T]TTTTTTTTTGTTTTT | 10138 |
rs368652671 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42202631 | TATTTCAATCTAAAT[A/G]GCATAACTTTTATTT | 10138 |
rs368679839 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42173064 | AGAGAGAGAGAGAGG[C/G]AGAGAGAGAAAGAGA | 10138 |
rs368786630 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42176076 | ACATGGCGAAACTCC[A/G]TCTCTACTAAAAATA | 10138 |
rs368800591 | snp | C/T | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239081 | AGTCCTTTTTAAATA[C/T]AAGGAGTTTGCATGT | 10138 |
rs368828621 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42181642 | CCCTGCTGTTCTTAT[A/G]TAATAAATAATTCAA | 10138 |
rs368895823 | snp | A/G | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42240109 | AGGACTCAAAGTACT[A/G]TGCACATGGCCTCAT | 10138 |
rs368907791 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42188114 | AACTATGAGAAAATA[A/C]ATGTTTTGGAGTAGT | 10138 |
rs368919573 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42228186 | CCAGCCGCCCCGTCC[G/T]GGAGGGAGGTGGGGG | 10138 |
rs368931884 | snp | A/G | 0.167158 | 0.235875 | intron-variant | YAF2 | GRCh38.p7 | 12:42227897 | CGGGAGGTGAGGGGC[A/G]CCTCTGCCCGGCCGC | 10138 |
rs368934704 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42197261 | CTAGACTGGTGTTCT[G/T]CCTTTGGCTATGAAC | 10138 |
rs369006978 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42159862 | TGTTCAATGACAATA[A/G]CACTAAACCTGAATT | 10138 |
rs369020628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42204720 | ATCCACATACGATGA[C/T]GTATTATTATTTGGC | 10138 |
rs369093544 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42207466 | ATGCCACAAGATAAA[A/T]TATTAATAATATTAT | 10138 |
rs369175062 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42185120 | GAGGCAAAGGCTGCA[A/G]TGGGCCAAGATCGCG | 10138 |
rs369424214 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42216658 | TTCAACTCAAATCAT[C/G]TGTACAAATGACTAT | 10138 |
rs369452861 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42161254 | ATTGTTATGACTGAA[C/T]GCATGACCATTTTGA | 10138 |
rs369464530 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42185431 | CAACAGGGCTTGAGA[A/G]GACTGGCTTAAATTT | 10138 |
rs369465353 | in-del | -/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42165080 | AAAAAAAAAAAAAAA[-/G]AAAAGAAACTACTTG | 10138 |
rs369485746 | snp | A/G | 1.6861e-05 | 0.00290348 | synonymous-codon, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160819 | GATCCACATTTTTCA[A/G]TCTTGGCCTAAACAT | 10138 |
rs369508538 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42193541 | CAGGATCTCACTCTG[C/T]CACTCAGGCTAGAAT | 10138 |
rs369535274 | in-del | -/G | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42225215 | CTTTTTGATGGGGTT[-/G]TTTTTTTTCTTGTAA | 10138 |
rs369537894 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42227175 | GCTGGAGGAGCGGAC[A/G]GGCCCCACGGGGCCC | 10138 |
rs369576710 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42228939 | ATTGAGAACGGGCCA[G/T]GATGACAATGGCGGC | 10138 |
rs369644014 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42176065 | CAGCCTGGCCAACAT[A/G]GCGAAACTCCGTCTC | 10138 |
rs369686050 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42171717 | CTAACACTTTGGAAA[A/G]CTGAGGTGGGTGGAT | 10138 |
rs369700154 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42214151 | TTTTACCCACTTGCT[C/T]ACCTTCATCTGATGC | 10138 |
rs369792960 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YAF2 | GRCh38.p7 | 12:42203887 | TTAGATATGCTTTTG[C/T]GGAACAGCTAATCCC | 10138 |
rs369794442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42177041 | CAGCCACTGTGATCC[C/T]TCCAAATGTAAATCA | 10138 |
rs369886858 | in-del | -/ACA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42205874 | TCAAATTTTGATACA[-/ACA]CTTTTGTTGTGATTT | 10138 |
rs369912923 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42181582 | CTCTACAGGTAGCCT[G/T]GTATAATCATAAACT | 10138 |
rs369952201 | in-del | -/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42229416 | TTATCAATAAAAAAA[-/T]AAATTAAAAAAAAAA | 10138 |
rs370042977 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42223947 | CTTAAAACCTAGATG[A/T]TGGGTTGATGGATGG | 10138 |
rs370084605 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157169 | GTCCAAGATCAGGGA[C/G]CCCATCTGATGAGGG | 10138 |
rs370095668 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42181039 | TCTTTGATACACCTA[A/G]CTCTGGGCAACTGAA | 10138 |
rs370217013 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42228817 | CCCGCCCGGCCAGCC[A/G]CCCCGTCCGGGAGGT | 10138 |
rs370261463 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42207689 | CAAGGTCAGGCGATC[A/G]AGACCATCCTGGCTA | 10138 |
rs370348206 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42217249 | TTCTATCCAGTAAAA[C/T]GGGTATAATTTTTTT | 10138 |
rs370356952 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42236921 | CAGAGTTATTATACT[A/G]CAAGCTTACAATAAA | 10138 |
rs370385644 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42185794 | GTAAACATAACTTTT[A/C]TATGAACTAGGAAAC | 10138 |
rs370454475 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42186392 | AAAATAAATAAAAAT[C/T]AAATATGGTATATAA | 10138 |
rs370472867 | snp | A/G | 0.33303 | 0.235809 | intron-variant | YAF2 | GRCh38.p7 | 12:42227830 | CTGGCCAGCCGTGCC[A/G]TCCGGGAGGGAGGTG | 10138 |
rs370599118 | snp | C/T | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238894 | GATTGTCAACCCTAA[C/T]TTAGAGGAATTGAAA | 10138 |
rs370655623 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42205034 | TAATATGGTATGTGA[A/G]TATCTCAATAAAGTT | 10138 |
rs370745201 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42196020 | TGAGGTCAGGAGTTG[G/T]AGACCAGCCTGGCCA | 10138 |
rs370850927 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42201509 | GGACACAAATCCACC[A/G]AATATTAAAGACATT | 10138 |
rs370911719 | in-del | -/AAGA | 0.0217236 | 0.101931 | intron-variant | YAF2 | GRCh38.p7 | 12:42230289 | AAAGAGAAGAAAGAG[-/AAGA]AAGAAAGAAAGAAAG | 10138 |
rs370939224 | snp | A/G | | | intron-variant, utr-variant-5-prime | YAF2 | GRCh38.p7 | 12:42237524 | CAGTGTCATGGGAGG[A/G]GGCGGCAGCCGCAAG | 10138 |
rs371001861 | snp | C/T | 0.000124417 | 0.00788625 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42237587 | GGCGCGAGGGGCAGG[C/T]CCGGGACTCACCGGG | 10138 |
rs371040867 | snp | C/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232848 | CTTTTTACCTAACCA[C/T]AATAATAATACTGTG | 10138 |
rs371088422 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42223183 | TTTATAAAACTATCA[C/T]AGTTGGGTGAAAGGT | 10138 |
rs371102069 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42173818 | AAAACTTGCTTTTAT[C/T]ATGTGCTATTTTATC | 10138 |
rs371151577 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42178913 | ACCCCTTTAGCCAGG[G/T]GTGGTGGTGCGTGCC | 10138 |
rs371155809 | snp | C/T | | | intron-variant, missense, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42199231 | AGGCTCTCTTCCTGT[C/T]ATCTCTGGCAAAAGG | 10138 |
rs371158321 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42159283 | TATTTTTAAGTTCAT[G/T]TACAATTCAGAAGTC | 10138 |
rs371352926 | in-del | -/TCTTA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42220328 | TGAGAAAAAGAATTA[-/TCTTA]AGGAAAAAATAAAAC | 10138 |
rs371375193 | snp | A/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42158922 | ATGTTAAAAACAGAA[A/T]AAGACAAAAAAATTC | 10138 |
rs371392128 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42197199 | CTGTTTAGCAAGTTG[C/T]TAGCTTGTTAGCAGT | 10138 |
rs371396488 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42220521 | ATTAGTGAAGAGACT[C/T]TGGGCTGTGGGGGAA | 10138 |
rs371407960 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42209695 | CAATATAAGTATTTA[C/G]TTCAAAAAAGCAACA | 10138 |
rs371439623 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42191950 | CAAAAATTAGCCAGA[C/T]GTGCTCACTTGAACC | 10138 |
rs371478628 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42165986 | GCGGTGGCGTGATCT[C/T]GGCTCAATGCAACCT | 10138 |
rs371555379 | in-del | -/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42228147 | GTCCGGGAGGGAGGT[-/G]GGGGGGGTCGGCCCC | 10138 |
rs371578330 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42216992 | TAAACACATCTATAA[C/T]ACATTCATTTCTGTC | 10138 |
rs371609080 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42184301 | TAATTTCAACTTTAA[A/G]GACTTATTATTATTA | 10138 |
rs371759011 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42187792 | TTTGGCCTTCCCACA[C/T]TGAATATGGCTGACT | 10138 |
rs371860187 | in-del | -/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42179210 | GCATTGGCTCACACC[-/G]TGTAATCCCAGCACT | 10138 |
rs371885898 | snp | A/C/G | 0.000139655 | 0.00835512 | intron-variant, nc-transcript-variant, missense, synonymous-codon | YAF2 | GRCh38.p7 | 12:42210442 | GAATCTTCCTGATGG[A/C/G]CATCCACTGGAACTG | 10138 |
rs371887311 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42228251 | GGAGGGAGGTGGGGG[G/T]GTCGGCCCCCCGCCC | 10138 |
rs371905892 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42228082 | GGGGCGCCTCTGCCC[A/G]GCCGCCCCTACTGGG | 10138 |
rs371952464 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42200617 | TTAAGGAAAAGCATA[C/T]AGTTCCATAAAGCTA | 10138 |
rs372061648 | in-del | -/G | 0.0119091 | 0.0762411 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42210311 | GACAAAATTTGGGGG[-/G]AAAAAAAATCTCAGG | 10138 |
rs372086173 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42181800 | ATGAACTGGGTAAAT[A/G]AATTTATAACTGTGA | 10138 |
rs372088503 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42226431 | ATTTTGGAGGCCAAG[G/T]TGAGAGGATTGCTTT | 10138 |
rs372094999 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42202124 | CCCCATCTAGAAAAC[C/T]AATTCGACAGTCTAC | 10138 |
rs372097165 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42171049 | CCAGGCTGGAGTGCA[C/G]TGGCGTGATCTCGGC | 10138 |
rs372101850 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42207467 | TGCCACAAGATAAAT[A/T]ATTAATAATATTATA | 10138 |
rs372107497 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | YAF2 | GRCh38.p7 | 12:42193255 | GGGAGGCGGAGGCTG[C/T]AGTGAACCGAGATTG | 10138 |
rs372141713 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42161166 | ACCATGGAGGAAGGT[A/G]ATAAAAGCTAAGGTT | 10138 |
rs372149820 | snp | A/G/T | 3.31067e-05 | 0.00406847 | missense, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160617 | CCATTCAATGATGAG[A/G/T]CTTCTCCTCTGGGTG | 10138 |
rs372196781 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42225352 | TTTTGCTGTGCAGAA[A/G]CTCTTTAGTTCAATT | 10138 |
rs372210539 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42213985 | AGAATAGCCCAACTA[A/G]TCTTTCTATTTACAC | 10138 |
rs372344595 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42186606 | CGCTCGAACCCAGGA[G/T]GTGGAGGTTGCGGTG | 10138 |
rs372350484 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42208199 | TTGGGAGGCCGAGGC[A/G]GGCAGATCACTTGAG | 10138 |
rs372352873 | snp | C/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233988 | CCAGCCTGGCCAGCA[C/T]AGTGAAACCCCATCT | 10138 |
rs372356763 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | YAF2 | GRCh38.p7 | 12:42227911 | CGCCTCTGCCCGGCC[A/G]CCCCTACTGGGAAGT | 10138 |
rs372465847 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42158519 | CTCCCAAAAACCCTA[C/T]AAATTAGATGTGATT | 10138 |
rs372470041 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42183768 | GGTGGCTACACTAAA[C/T]AACAGATTTTCAATG | 10138 |
rs372492560 | in-del | -/ATT | | | intron-variant | YAF2 | GRCh38.p7 | 12:42210940 | AGCCACCAGGCTATT[-/ATT]TCATTTTGCTGAAAC | 10138 |
rs372562989 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42220600 | AAATCACTTTGCCTA[C/T]TCCACAAATGCACCA | 10138 |
rs372567914 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42177692 | CTTTCTACTTCTGCC[C/T]GAGGGTTTCCCCTGC | 10138 |
rs372585161 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42171799 | TCTCTACAGAAAATA[A/C]AAAAAAAAAAAAAAA | 10138 |
rs372697525 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42212978 | CAAAGGTCTTATATG[C/T]TTATAGTGATAAAAC | 10138 |
rs372745052 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42236288 | TAAATCACAAATCAC[A/G]GGTCCAAAAATAGTA | 10138 |
rs373124332 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42217549 | TTTATCAGTACCTAC[-/A]CAAGACACTGTGATG | 10138 |
rs373181389 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42203514 | CTATTAAGCATGATG[C/G]TTTCTATTTGAAAGG | 10138 |
rs373217285 | snp | C/T | | | missense, nc-transcript-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42161644 | TATTCTTTTTGCTAG[C/T]TGTTTCCTTTTCACT | 10138 |
rs373234253 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42206408 | GAGGTCAGGAGTTCG[A/C]GACCAGCTTGGCCAA | 10138 |
rs373244779 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42177929 | ATTTTCTTCAAAGCA[C/T]TTCTCTACCTACTAC | 10138 |
rs373397734 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42223473 | AAAGTAATCAATCAA[A/C]CTGGAAATTGGCCAT | 10138 |
rs373435357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42200486 | ACCAGTATCAAGAAT[A/G]AATGAAGATTAAAAC | 10138 |
rs373439540 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42228822 | CCGGCCAGCCGCCCC[A/G]TCCGGGAGGTGAGGG | 10138 |
rs373451402 | in-del | -/CACA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42192355 | CCACACACACACACA[-/CACA]AAAATTAGTTGGGCA | 10138 |
rs373474959 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42202851 | CATGTTGGCCAAGCT[A/G]GTCTTGAACTCCTGA | 10138 |
rs373534866 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42198376 | TCACTTTGAGCTCAG[A/G]AGTTTGAGACCAGCC | 10138 |
rs373690317 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42230160 | TACTCAGGAGGCTGA[A/G]GCAGGAGAATCGCTC | 10138 |
rs373690982 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | YAF2 | GRCh38.p7 | 12:42207862 | TGCCACTGCACTCCA[C/G]CCTGGGCGACAGAGC | 10138 |
rs373800249 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42181494 | TTGAATAACTGCTCC[A/G]GGAACAGCTTACTGC | 10138 |
rs373802629 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160018 | CAGGAACAATAATTA[A/G]TAAAACGTGTCAAAA | 10138 |
rs373854995 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42202371 | CCAGCTCAAGCCAAA[A/C]TATTAACATTCCTCA | 10138 |
rs373858503 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42224915 | GACTGCTGGATCAAA[C/T]GGTATTTCTGGTTCT | 10138 |
rs373862311 | in-del | -/GT | | | intron-variant | YAF2 | GRCh38.p7 | 12:42201532 | AGACATTGTGTGTGT[-/GT]CTCCTCCTAGGTATG | 10138 |
rs373901378 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42169099 | CTCTCAGTTGTGTCC[G/T]TGTCTTCACTTCTAC | 10138 |
rs373918104 | snp | A/G | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232936 | ATAAAGGAAAGATCT[A/G]CTAACACTAAACCTC | 10138 |
rs374000663 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42207659 | GCACTTTGGGAGGCC[A/G]AGGCGGGCAGATCAC | 10138 |
rs374034272 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42174084 | CAAAATATTTCAATA[A/T]TTCATACCTCAAAAA | 10138 |
rs374036079 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42227711 | TGGGAAGTGAGGAGC[A/G]TCTCCGCCCGGCAGC | 10138 |
rs374042176 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42219238 | CAACACAATTTGAAA[C/T]CACTGGGCCTCCTGA | 10138 |
rs374092538 | snp | A/G | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42231604 | GTATTTTGTACTTTG[A/G]TGGATTACCCATTAC | 10138 |
rs374098783 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42167761 | CTATAATCCCAGCAC[G/T]TTGGGAGGCCAACGC | 10138 |
rs374182436 | snp | A/T | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239953 | AGAGTGAGAGGTTGC[A/T]GTGAGCCGAGATCGT | 10138 |
rs374188638 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42164156 | CCAACTACAGTCCAT[C/T]ATCTACTTATTCACA | 10138 |
rs374344258 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42173258 | GGGGCTCCACGGTCT[A/G]TATGTATTTAATTTT | 10138 |
rs374358311 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42195313 | GTAAAGCACAGGTTA[A/C/T]GGACAAATTTTAATA | 10138 |
rs374370440 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42237140 | TTCCAGAAGTACATG[C/T]AGAAAAATAAGTTTT | 10138 |
rs374379638 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YAF2 | GRCh38.p7 | 12:42173900 | TAGAATGTCCACAGC[C/T]TTCCATCTGTACCGA | 10138 |
rs374475335 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42191560 | TACTTTTAACAAGCA[C/T]GTTTGGTCTTGTTTT | 10138 |
rs374512625 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42227896 | CCGGGAGGTGAGGGG[C/T]GCCTCTGCCCGGCCG | 10138 |
rs374602892 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42210770 | TTCACTAGATAACTA[C/T]ATATACACGTATCAA | 10138 |
rs374646310 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42214849 | TCTCTACTAAAAATA[C/T]GGAAATTAACCAGGC | 10138 |
rs374682971 | snp | C/G | 0.000307953 | 0.0124049 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42237696 | CCCAGTAACCCTCAT[C/G]CGAGGACGGCTTCGG | 10138 |
rs374765987 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42183667 | CAAGCCACCTTCACA[G/T]GAAAAAATTACAAAG | 10138 |
rs374770597 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42185967 | CACTCTGGGGAGTCC[A/G]AAGCAGGTGGGTAAT | 10138 |
rs374829523 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42187801 | CCCACACTGAATATG[G/T]CTGACTTGTATAACC | 10138 |
rs374906012 | in-del | -/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42218184 | ATCAGGCTACTAGGA[-/G]AACACACACACACAC | 10138 |
rs374922362 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42179025 | GCCTCTGCACTCCAG[C/G]CTGTGAAACAAAGCG | 10138 |
rs374948198 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42213281 | ACTTGGAAGCAGGTG[C/T]TCTAAGGTCTGCTGA | 10138 |
rs375008305 | in-del | -/GTTTTT | | | intron-variant | YAF2 | GRCh38.p7 | 12:42165452 | TCGAATGGCCAAAAG[-/GTTTTT]GTTTTTGTTTTTGTT | 10138 |
rs375069269 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42228839 | CCGGGAGGTGAGGGG[C/T]GCCTCTGCCCGGCCA | 10138 |
rs375099927 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42215329 | TAATTCCAGCACTTT[A/G]GGAGGCTGAGGTGGA | 10138 |
rs375205559 | snp | A/G | 0.000165604 | 0.00909805 | synonymous-codon, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160679 | ATCAGAGCTAGAGCC[A/G]CTTTGACTGTGTTGA | 10138 |
rs375220651 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42207465 | TATGCCACAAGATAA[A/T]TTATTAATAATATTA | 10138 |
rs375220735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42194289 | TTCATTCACTACTCA[C/T]TCACTCACCCAGAGC | 10138 |
rs375307735 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42211386 | GAGCGGAGATCGTGC[C/T]ACTGAACTCCAGCCT | 10138 |
rs375410158 | snp | A/G | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234324 | AAAAATTTCCTGTCA[A/G]TTTGACATTTACTAC | 10138 |
rs375411427 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42221384 | GAGACCAGGCTGGAC[A/G]ACATAGCAAGACCTC | 10138 |
rs375471984 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42193293 | GCACCCCAGCCTGGG[C/T]GACAGAGTAAATGAG | 10138 |
rs375484071 | snp | C/T | 0.00324516 | 0.0401504 | intron-variant, utr-variant-3-prime, splice-acceptor-variant, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42235757 | AGAGCTTAGATGTAC[C/T]GGTAAAAAAAAAAAA | 10138 |
rs375502767 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42174534 | CTTTGGATACCTCTT[A/G]TCTACGCTAACCCTC | 10138 |
rs375569466 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42226074 | GTGGTTTGTAGTTCT[C/T]CTTGAAGAGGTCCTT | 10138 |
rs375579322 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42218051 | AACAGTAAAAAATTC[G/T]GCTTTTACTGGCTTA | 10138 |
rs375604271 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42198822 | AGAGTAACAGCAGAA[C/T]TACATAACACCAAAG | 10138 |
rs375634257 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42177693 | TTTCTACTTCTGCCC[A/G]AGGGTTTCCCCTGCT | 10138 |
rs375707440 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42204508 | AATCTAGAGATCATG[G/T]AATGCATATGGGAGA | 10138 |
rs375818792 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42228333 | CCGGCCAGCCACCCC[A/G]TCCGGGAGGTGAGGG | 10138 |
rs375838297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42187052 | CCTACATAGAACCTA[A/G]TAATACAATATTGGT | 10138 |
rs375850547 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42208540 | AGCTAACTATAACCA[A/C]AAAAATGGTTAAGAT | 10138 |
rs375863376 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42227956 | CCCAGCCAGCCACCC[C/T]GTCCGGGAGGGAGGT | 10138 |
rs375919542 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42215082 | TCTGTAACTCCATTA[C/T]CTAGCCCAGCACCTG | 10138 |
rs375939291 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42162976 | TAGTTAATGGCTGAG[G/T]TTAAAAAAGAAAAGG | 10138 |
rs375941296 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42185917 | TTAAAAAGTCAGGCT[G/T]GGCCGGGCACAGTGG | 10138 |
rs375947102 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42206976 | TGCTTTACCTTTTTT[C/T]TCTCTCTCTCCATAT | 10138 |
rs376005827 | in-del | -/A | | | intron-variant | YAF2 | GRCh38.p7 | 12:42237310 | ACCCAGAATGGGGAG[-/A]GGGGCATTACACCCA | 10138 |
rs376053874 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42201623 | TGAGCCCAGGCTGGA[A/G]GGCAGTGGCACAATC | 10138 |
rs376057970 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42224681 | TGGTTTCCAGCTTCA[G/T]CCATGTCCCTGCAAA | 10138 |
rs376058975 | snp | A/G | 0.333261 | 0.235728 | intron-variant | YAF2 | GRCh38.p7 | 12:42227737 | GCAGCCACCCCGTCC[A/G]GGAGGGAGGTGGGGG | 10138 |
rs376160649 | snp | A/C | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232203 | TGTACATGGTGGTGA[A/C]TATTACAATGAAGAT | 10138 |
rs376176473 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42188053 | CAGGAGAAACCCAGA[A/G]CCAGAACCACCCAGC | 10138 |
rs376189144 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42228185 | GCCAGCCGCCCCGTC[C/T]GGGAGGGAGGTGGGG | 10138 |
rs376313101 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42240326 | CCCAGGTTAAATGGT[G/T]TTTCTTTGATGAGCA | 10138 |
rs376344874 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42172064 | TTTTTATTCTTCCAA[A/T]GCTCTATGCTCTTTC | 10138 |
rs376377205 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42226937 | CGGCCATGGTGGCCG[C/T]GGGTGGTGGTTGGCG | 10138 |
rs376378716 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42214246 | GGCTTTCAACTTGCC[A/G]TTAACTACAACTCTT | 10138 |
rs376577462 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42212866 | CAGGGGTACTACACA[C/G]ACCTCCATTTCTAAT | 10138 |
rs376578389 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160655 | CCTGGACATTCCTCT[C/G]TCTGTGTTATCAGAG | 10138 |
rs376602612 | in-del | -/GATT | | | intron-variant | YAF2 | GRCh38.p7 | 12:42198730 | TTTCAGACTACAATT[-/GATT]AATAGTTAAGATAAG | 10138 |
rs376657664 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42224269 | TGCATATGTTTCCCA[A/G]TAAGCATGTATTTAT | 10138 |
rs376669913 | snp | G/T | 1.82161e-05 | 0.0030179 | intron-variant | YAF2 | GRCh38.p7 | 12:42160868 | ACTAGCTTTTCCCTC[G/T]ACCAAATTTCTGAGC | 10138 |
rs376781030 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42158547 | ATTACCATTATTAGC[C/T]CTGTTTTATAGATGG | 10138 |
rs376786165 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42214141 | TGATCTGGCATTTTA[C/T]CCACTTGCTCACCTT | 10138 |
rs376791205 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42184092 | ACCGTTAAGACCTGA[A/T]TTTAAAATATTTAGC | 10138 |
rs376831455 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42222893 | AGTAGTGGCCATTAC[C/T]GTTAAGGAATAAATG | 10138 |
rs376836378 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42170967 | AGAGCACTAGAGCAA[C/T]GTAAGTGGTCAGGAA | 10138 |
rs376882542 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42178232 | CACTTGTTTTCAACC[C/G]TGGCTACACATTAGC | 10138 |
rs376883094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42236807 | CGTATAAGAATCAAG[A/G]AGCTCGATAACTAAG | 10138 |
rs376890544 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42198728 | GGTTTCAGACTACAA[C/T]TGATTAATAGTTAAG | 10138 |
rs376897111 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42222794 | GCATTGTTGAGAAGA[C/T]TAAATGGTTTTAATT | 10138 |
rs376932767 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42199583 | TTCAAAAGGCACTGG[A/G]ATTCTCACATTATAA | 10138 |
rs377011563 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42205336 | TGCAAACAACCAGCT[C/T]TGACTGATCACGACA | 10138 |
rs377017751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42173474 | TTAAATGACACGACA[A/G]TTTGGCATTTGCTTT | 10138 |
rs377146602 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42207165 | AGATTGAACAGAATC[A/G]TACAAAGACATGCAG | 10138 |
rs377212332 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42190098 | CTGTAATCCCAGCAC[C/T]TTGAGAGGCTAAGGC | 10138 |
rs377271260 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42201342 | GAAAATTGATAGCTC[A/G]TACGTTTTCAACTGC | 10138 |
rs377476308 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42179974 | ATTTTTTCTTTTACA[A/G]TTCAGCTTCCATTTC | 10138 |
rs377525156 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42223239 | AAAGTTACATATAGC[G/T]CCAGCATACTATGTA | 10138 |
rs377527943 | in-del | -/A | 0.27893 | 0.24832 | intron-variant | YAF2 | GRCh38.p7 | 12:42166830 | TGTTCAATGAAAGTT[-/A]AAAAAAAAAAAAAGG | 10138 |
rs377532776 | snp | A/G | 0.00252349 | 0.0354313 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238160 | GCGCTGTTACCTGGT[A/G]GGGCTCTTCTTGTCT | 10138 |
rs377622477 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42185152 | CACTGCACTCCAGCC[C/T]GGGCAACAGAGCCAG | 10138 |
rs377720757 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42168342 | CACCACCATGCCCAG[C/T]TAATTTTTTTTGTAT | 10138 |
rs377722168 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42191742 | TGTTCATTTTTCCCC[A/C]CCCTGCCCAATACCA | 10138 |
rs377722950 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42214055 | ACAGAGCACTTCCAC[A/G]CTTAAACTCATTAAA | 10138 |
rs377747490 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42195348 | AAGAATGAAATTGTG[A/G]CATTAAACATAACTT | 10138 |
rs377751701 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42237190 | AATCAGATACTTTTC[C/T]TTCTTTAGGAACGAA | 10138 |
rs386376301 | in-del | -/AA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42186190 | CCAAACTCTGTCTCA[-/AA]AAAAAAAAAAAAAAA | 10138 |
rs386376302 | in-del | -/AA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42186210 | AAAAAAAAAAAAAAA[-/AA]AGGCTGGGCTTGGTG | 10138 |
rs386762507 | multinucleotide-polymorphism | CT/GG | | | intron-variant | YAF2 | GRCh38.p7 | 12:42176366 | CCTCAAGTGATACTC[CT/GG]GCCTCAGCCACCCAA | 10138 |
rs386762508 | multinucleotide-polymorphism | CC/TG | | | intron-variant | YAF2 | GRCh38.p7 | 12:42191596 | TTTCTCTGAATTTTT[CC/TG]TTGTTTTCCTTCTTT | 10138 |
rs386762509 | multinucleotide-polymorphism | GC/TG | | | intron-variant | YAF2 | GRCh38.p7 | 12:42201819 | TCAAGTGAACCATCT[GC/TG]CTTGGTCTCCCCAGA | 10138 |
rs386762510 | multinucleotide-polymorphism | AG/GA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42208930 | AAAGTTTTGTAAAAC[AG/GA]CTATAAGCAGGACAC | 10138 |
rs397718085 | in-del | -/G | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42213063 | AGATGTCATTAAGAG[-/G]CCAGGCACGGTGGCT | 10138 |
rs397780110 | in-del | -/CA | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42223356 | ACACACACACACACA[-/CA]TATATATACACACAA | 10138 |
rs397809009 | in-del | -/G | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42221474 | ACTTGGGAGGTTGAG[-/G]CTTGAGCCCAGGAGT | 10138 |
rs397813385 | in-del | -/TG | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42161044 | GCAACCAAAAAACTG[-/TG]ACAGCCTAGAAGTAG | 10138 |
rs398019262 | in-del | -/T | 0 | 0 | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42157074 | CCACTTTTTTTTTTT[-/T]GCTATAACAGAATAC | 10138 |
rs398019263 | in-del | -/A | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42179809 | AAAAAAAAAAAAAAA[-/A]GAAATCAGTAGTATT | 10138 |
rs398019264 | in-del | -/A | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42209589 | AAAAAAAAAAAAAAA[-/A]GTGCTAGACAATTAA | 10138 |
rs398019265 | in-del | -/A | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42211451 | AAAAAAAAAAAAAAA[-/A]GTCATCCAGGCACAG | 10138 |
rs527252469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42192905 | TCCCTAAGATAATGA[A/G]GCTGACAAATACTTA | 10138 |
rs527337786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | YAF2 | GRCh38.p7 | 12:42237507 | CCTCCCGCCGGGTCC[A/G]CCAGTGTCATGGGAG | 10138 |
rs527352104 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42228414 | GCCAGCCGCCCCGTC[C/T]GGGAGGGAGGTGGGG | 10138 |
rs527371161 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | YAF2 | GRCh38.p7 | 12:42185201 | AAACAAACAAACAAA[A/C]AAAAAAACAGAACTA | 10138 |
rs527398701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42229916 | GACTGACTCTACATA[C/T]ATAGAATCAATATGA | 10138 |
rs527398956 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42221569 | ATCTCTTTAAAAAAA[A/T]TTTTTTTTAAGTGAC | 10138 |
rs527422491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42178216 | ATCTGTGATCCTATC[A/G]CACTTGTTTTCAACC | 10138 |
rs527457349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42171181 | ATTTTTAGTAGAGAC[A/G]GGATTTCACCATATT | 10138 |
rs527484565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42171841 | TACTGGTGCGTGCCT[A/G]TAGTCCCAGCTACCC | 10138 |
rs527508347 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42168260 | CTCAGCTCACTGCAA[C/T]CTCCGCCTTGTGGGT | 10138 |
rs527511913 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42214665 | CTGTTGTTGCCACAC[A/T]CTGCAATGATTTTTT | 10138 |
rs527618500 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42165051 | CAGAGTGAGACCCTG[C/T]CTTCTGGAACAAAAA | 10138 |
rs527651237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42176827 | AAAAATGTAGCTAGG[C/T]GTGGTGCTGGGCGTC | 10138 |
rs527688492 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42169555 | AGTAGCTAGGACTAC[A/C]GGCATGCCCCACCAC | 10138 |
rs527738977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42212854 | GACCCATTCAAACAG[A/G]GGTACTACACAGACC | 10138 |
rs527782632 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42174572 | GTGCTACTCAAAAAG[C/T]GTAGTCAACGAATGA | 10138 |
rs527822970 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42172225 | CTTGAAAGAAAGATA[A/C]AAGGACTTTTGAGTT | 10138 |
rs527869469 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42163311 | ATTAAAAGCTAAGCA[C/G]TCTGATTTTATCCTT | 10138 |
rs527915642 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42206379 | CTTGGGAGGCTGAGG[C/T]GGGCAGATCACCTGA | 10138 |
rs527940246 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42200880 | GCTATTTACTAGCTA[A/T]GAGAGTGAGTAGGTT | 10138 |
rs527950082 | snp | C/T | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238832 | GCCATTGCTACATGC[C/T]TTAAAGCACTGTCTG | 10138 |
rs527976137 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, missense, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42199219 | CAAATGGTAACCAGG[A/C]TCTCTTCCTGTTATC | 10138 |
rs527998225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42200186 | AATAATAGAAGTGGG[A/G]TCTTCATCAGTATTT | 10138 |
rs528001579 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42176068 | CCTGGCCAACATGGC[A/G]AAACTCCGTCTCTAC | 10138 |
rs528038980 | snp | C/G | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42235244 | TTGGCTTTAGTACTT[C/G]CCAACCTTACTCTGG | 10138 |
rs528079674 | snp | A/G | | | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42156945 | TTTCACTTAATTTTC[A/G]AAGTACAGTGCGGAA | 10138 |
rs528174040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42204612 | AACAACACAGGACTA[C/T]AATAGTTCACAGAAG | 10138 |
rs528183698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42197510 | TAAGTAACAGCTAAA[C/T]GCTGCACTAACTACG | 10138 |
rs528209218 | in-del | -/A | 0.0197687 | 0.0974348 | intron-variant | YAF2 | GRCh38.p7 | 12:42182375 | CAAAACACAAATGTG[-/A]AAAAAAAATCAATCA | 10138 |
rs528245477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42190285 | GGAAGCAGAAGGTGC[A/G]GTGAGCTGTGACAGC | 10138 |
rs528341505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42226419 | TGTAATCCCAACATT[C/T]TGGAGGCCAAGGTGA | 10138 |
rs528349222 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42215708 | CAGGCAGATCACTTG[A/G]GGTCAGGAGTTCAAG | 10138 |
rs528377873 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42182903 | GCACATCTCATTTTA[C/T]TGTGCATTACTTTAT | 10138 |
rs528413332 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42176357 | AACTTCTGGCCTCAA[C/G]TGATACTCCTGCCTC | 10138 |
rs528448441 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42216921 | CTTCACTATGACCCA[A/C]CTTCCTGCCTCCCAC | 10138 |
rs528555456 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232692 | AGAATCAGTGCCAAA[A/C]CTCAAATTTGAAGAC | 10138 |
rs528614657 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42181277 | AATGTGTGCTTATTC[C/T]TGTTACACAGTTTAC | 10138 |
rs528645225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42182095 | GCAAAATATGCTCTT[C/T]TGTGTAAACTGATGA | 10138 |
rs528652077 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42174663 | GGGTGATTTTTTTAT[G/T]CATGCTAAAAGCACT | 10138 |
rs528659711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233413 | CCACTACTAGATGAA[A/G]TACCAATAAGACACC | 10138 |
rs528666931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42167372 | ATAGGAAAAAATCAA[A/G]TAACTAAGATCCCGT | 10138 |
rs528679684 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42224986 | GAACTAATTTACACT[C/G]CCACCAACAGTGTAA | 10138 |
rs528803930 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42211381 | GCAGTGAGCGGAGAT[C/T]GTGCCACTGAACTCC | 10138 |
rs528808915 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234824 | ATCCCCCATCTCTAC[-/A]AAAAAATAAGAAAAT | 10138 |
rs528848658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42179588 | TGAGCTCAGGAGTTT[A/G]AGACCAGCCTAGTAA | 10138 |
rs528864984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42230525 | TCACATAGGTTTCAA[A/G]AAAGATAATGAAGAT | 10138 |
rs528899404 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42223401 | AAAAGGCTTTACCCA[G/T]CAATGAAGTGCCAGC | 10138 |
rs528974268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42216656 | GCTTCAACTCAAATC[A/G]TGTGTACAAATGACT | 10138 |
rs529015392 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157486 | GCAGGAAGTTTAAAA[A/G]AGCGAGTGGCGGAAG | 10138 |
rs529041256 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42173665 | TTAACCCAACAGACT[G/T]CTACAGCACCTTCTC | 10138 |
rs529057260 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157916 | TGAGCCATCACACCC[A/G]GCCTATCTTCACTCT | 10138 |
rs529091927 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42189917 | TAGCGTATGTATTCA[C/T]TACAGCATATACTTT | 10138 |
rs529152564 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42222398 | TTTATTAAAGACAAA[C/T]GAGTGAAAAGATCAA | 10138 |
rs529180992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42203324 | CTTGTATCCAGCAAC[A/G]CTGAATTATTTTATT | 10138 |
rs529186155 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42202401 | ATGCTCCAGGAGGCT[A/C]CCTCACGATCCTTAC | 10138 |
rs529214516 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42195309 | TCACGTAAAGCACAG[G/T]TTACGGACAAATTTT | 10138 |
rs529245529 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42219312 | TTCTAACAGGCAAAC[C/T]TCTCTCCTCTTTACC | 10138 |
rs529263851 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42199516 | CACACACCTTTCTCA[C/T]TAGGATGAAATGAAA | 10138 |
rs529299594 | in-del | -/AAAT | | | intron-variant | YAF2 | GRCh38.p7 | 12:42196504 | GTTTCATAATAAAGA[-/AAAT]AAATAAAGTTTATAG | 10138 |
rs529302741 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42207619 | AAGTGTAGGCTGGGC[A/G]CGGTGGCTCATGCCT | 10138 |
rs529310045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42164949 | AGGTACGCGCCTGTA[A/G]GAGGCTGAGGTGGAA | 10138 |
rs529324411 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42215032 | AATAAATAAATAAAT[A/G]AATTCCATGAGAGTA | 10138 |
rs529341366 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42200410 | TTCTTATCCCTAGCA[C/G]CTAGTGCTTATCTGC | 10138 |
rs529346102 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42156975 | AACTTCTACCAATGA[C/T]TTACTAAATAGCTCA | 10138 |
rs529353469 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42200991 | TACAACAGTTAAGAT[A/T]CATAAAGGGCTTAAA | 10138 |
rs529427058 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42226273 | AAAATGAGACCTAAT[A/T]AGTGGCCACAAATGA | 10138 |
rs529472362 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238554 | CCCCCTTGGTACCCC[C/T]GGCTGCCGGGGACTG | 10138 |
rs529481284 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | YAF2 | GRCh38.p7 | 12:42177889 | CCAACTTCACTCCCT[-/A]ACTCTATCCTCCTTA | 10138 |
rs529481628 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42170824 | GCACTCTAGCCTGTA[A/G]ATCCACCTCTCCAAT | 10138 |
rs529544100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42185937 | GGGCACAGTGGCTCA[C/T]GCCTGTAATCCCAAC | 10138 |
rs529567131 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42186441 | ACTTTCCTGAGGGGG[G/T]CAGAGGGGTGGATCA | 10138 |
rs529637165 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42186246 | GGCCTGTAATCCCAG[A/G]ACTTTGGGAGGCAGA | 10138 |
rs529692034 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42211886 | AAACCCCGTCTCTAC[C/T]AAAAATACAAAAATT | 10138 |
rs529702417 | snp | C/T | 0.00291686 | 0.0380779 | intron-variant, synonymous-codon, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42235898 | TTCAGCCTGTTTCTT[C/T]TCTTCTGAGCTGCCA | 10138 |
rs529706524 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42179203 | GGCTGGGTGCATTGG[C/T]TCACACCTGTAATCC | 10138 |
rs529735352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42191978 | ACCCAGGAGGAGGAG[A/G]CTGCAGTGACCCAAG | 10138 |
rs529788623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42183427 | AGCTAAGATGTGACT[A/G]TAAAGAAAAGCTGTC | 10138 |
rs529806518 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42177576 | TTAATTGCCTCCTAC[A/C]AGCCTTATCTCCAAA | 10138 |
rs529883533 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42237346 | ACGAATTAAATCGCA[C/G]TAGCTAATGCCTCCC | 10138 |
rs529898257 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | YAF2 | GRCh38.p7 | 12:42227706 | CCATCTGGGAAGTGA[A/G]GAGCGTCTCCGCCCG | 10138 |
rs529907330 | in-del | -/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42159482 | TAATTTTACATAGTA[-/T]AAGTGGGGCTATACT | 10138 |
rs529964984 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | YAF2 | GRCh38.p7 | 12:42228034 | GTGGGGGGTCAGCCC[C/T]CCGCCCGGCCAGCCG | 10138 |
rs529968791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42214589 | CTCTTATCCTTCTGC[C/T]TTCTGATTAAATGCC | 10138 |
rs529974108 | in-del | -/G | 0.0433465 | 0.140692 | intron-variant | YAF2 | GRCh38.p7 | 12:42227796 | GTCCGGGAGGGAGGT[-/G]GGGGGGTCAGCCCCC | 10138 |
rs529977967 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42221485 | TTGAGCTTGAGCCCA[C/G]GAGTTTGAAGTTATA | 10138 |
rs529981379 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42167865 | CTCAGGAGTGGTGAC[A/G]CAGGCACATGCCTAT | 10138 |
rs529981797 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42171101 | GGGTTCAAGCAATCC[C/T]CCTGCCTCAGCCTCC | 10138 |
rs530022227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234935 | CGAGGCTGCAGTGAG[C/T]CTGGATGATGCCACT | 10138 |
rs530022657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42225737 | GTTCTATCGGTCTAT[A/G]TGTCTGTTTTGCTAC | 10138 |
rs530085354 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42226298 | AAATGAGATCATAAC[A/G]ATATTATACAACTTG | 10138 |
rs530180289 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42178988 | AGGCCAGGAGTTTGA[A/G]GTTATAATGAGCTAT | 10138 |
rs530264215 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42168775 | GGGCATATTTGCACA[G/T]TTACATGTCATTTGG | 10138 |
rs530298408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42161425 | ATCATCACATTTAAG[C/T]TTGTATTTCTGGCTT | 10138 |
rs530385146 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42163107 | CTTGAAGTAGAGCCC[A/C]AGAAACTGTATTTCT | 10138 |
rs530423308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42198306 | ATCAGAATGAAGCCA[A/G]GCACAGTGGCTCATG | 10138 |
rs530425168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42206239 | GTTATTTTACATAAA[C/T]ATTTATTGTTTCTGA | 10138 |
rs530508601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42167213 | TAAAACCTAGATGAC[A/G]GGTTGACAGTTACAG | 10138 |
rs530516691 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42203415 | TTCCTTTCCAATCCT[G/T]TTGGATTTTCTTTCT | 10138 |
rs530524321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42204059 | ACAGCACAGCAAGAC[C/T]CCATCTCTAAAAAAA | 10138 |
rs530690108 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233702 | ATTTTTAGTAGAGAC[A/G]AGATCTCACTGTGTT | 10138 |
rs530756033 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42190143 | AAGCCAGGAGTTTGA[C/G/T]TCCAGCCTGGGCAAC | 10138 |
rs530866541 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42182248 | GGAAGCAGAAGGCAT[G/T]AAATTCTGTTAACAT | 10138 |
rs530888803 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42186529 | AAAAATACAAAAATT[A/G]GCTGGGCATAGTGGC | 10138 |
rs530896080 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | YAF2 | GRCh38.p7 | 12:42202287 | TTTTTTAACAGAGGT[A/G]CTTACATAAAGCATA | 10138 |
rs530922342 | in-del | -/T | 0.00597247 | 0.0543191 | intron-variant | YAF2 | GRCh38.p7 | 12:42162514 | TCAAAATACAGTCTC[-/T]TAAGTTCTTAAGAGA | 10138 |
rs530928892 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | YAF2 | GRCh38.p7 | 12:42213416 | ATTATTTAAATTAAT[C/T]TGACCAGATTTTGAA | 10138 |
rs531071668 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42216757 | TCTTCCCTCTCAAAT[A/T]TTCCCCAGGCACCCC | 10138 |
rs531076533 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42187229 | TGGCACAATCATAGT[G/T]CACTGTGACCTCAAA | 10138 |
rs531076568 | in-del | -/A | 0.00132217 | 0.0256775 | intron-variant | YAF2 | GRCh38.p7 | 12:42230058 | GGTCAGGAGATGGAG[-/A]CCATCCTGGCCAACA | 10138 |
rs531113849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42231723 | AATATCAGAAATTAT[A/G]TTCATTGATACCACC | 10138 |
rs531153183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42166217 | TGCGCCTGGCCTCAA[A/G]TACATTTCTAATAGG | 10138 |
rs531154556 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42174497 | CCAAATTTCTAAACT[G/T]CAGAGTACCTCAGGA | 10138 |
rs531176347 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42224418 | ATTCTGGGATACATG[G/T]GCAGAACCTCCAGGT | 10138 |
rs531183851 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238538 | CGCTGTTCCCCCGTT[A/G]CCCCCTTGGTACCCC | 10138 |
rs531190941 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42224765 | CCACATTTTCTTTAT[A/C]CAGTCTATCATTGAT | 10138 |
rs531193726 | snp | A/C | 0.0501905 | 0.150254 | intron-variant | YAF2 | GRCh38.p7 | 12:42229227 | AGCATGCTCGTTAAG[A/C]GTCATCACCAATCCC | 10138 |
rs531258386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42217537 | TTGCAGTTCATTTTT[A/G]TCAGTACCTACACAA | 10138 |
rs531261012 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42222721 | CTATTTTATTGGTTA[C/T]ATTGGCAATGATCGC | 10138 |
rs531285599 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42185819 | GGAAACCAAAAACTT[C/T]GTATGACTTGCTTTG | 10138 |
rs531304389 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42178355 | ATTTTTCAAATCTCC[G/T]GGGCTGCTCCTATTG | 10138 |
rs531314507 | snp | C/T | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238977 | TGACAAAGCCAAGAG[C/T]CTAACTCTGTTTTAA | 10138 |
rs531343699 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42178897 | GCTTTAAAAAAAAAA[C/T]ACCCCTTTAGCCAGG | 10138 |
rs531464766 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157863 | CCTGGGCTCAAAATA[C/T]CTGCCTGCTTCAGCC | 10138 |
rs531514485 | in-del | -/TCTT | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42213986 | GAATAGCCCAACTAG[-/TCTT]TCTATTTACACATTC | 10138 |
rs531558855 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42165659 | TTTATTTTTAATAGA[C/G]ACGGGGTTTCACTGT | 10138 |
rs531564763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42207857 | GATCGTGCCACTGCA[C/T]TCCAGCCTGGGCGAC | 10138 |
rs531625558 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42213784 | GTGTGTGTATATTAA[C/T]GACCTTTTTATGGAA | 10138 |
rs531631960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42163569 | CTTTCTCTTTTTATC[C/T]TAGGCTTACCTAAAT | 10138 |
rs531686579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42206557 | GAGGTTGAAGTGAGC[C/T]GAGATAGCGCCACTG | 10138 |
rs531777231 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42221816 | AGGTTTTGAAAACAA[C/T]AGTAGTCTCAGCCCA | 10138 |
rs531790150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42164384 | GGAGGTCAATACATG[C/T]TGGCTTCATATATGC | 10138 |
rs531870279 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42178138 | TTGTATCAATAAAGA[A/G]AAATAAATATTTAAT | 10138 |
rs532070729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42193531 | TTTGTTGAGACAGGA[C/T]CTCACTCTGTCACTC | 10138 |
rs532154898 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42208572 | AATCTATAGCCAAAC[A/G]CTAGCCAATAAGGGT | 10138 |
rs532184988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42176860 | TAATCCCAGCTACTC[A/G]GGAGGCTAAGGCAGG | 10138 |
rs532186924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42184216 | GAGCTCTAAGGGACA[C/T]GTACAAGGAGATTAA | 10138 |
rs532257250 | in-del | -/AATAAAT | 0.00318978 | 0.0398085 | intron-variant | YAF2 | GRCh38.p7 | 12:42215927 | AGATTCCAGCTCAAA[-/AATAAAT]AAATAAATAAATAAA | 10138 |
rs532259227 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | YAF2 | GRCh38.p7 | 12:42227680 | AGGAGCCTCTCCGCC[C/T]GGCAGCCACCCCATC | 10138 |
rs532259775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42164940 | GGCCAGTAAAGGTAC[A/G]CGCCTGTAGGAGGCT | 10138 |
rs532349596 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232776 | ATAGTTGGTTTAAGC[G/T]TCTTTCAGAATGTGG | 10138 |
rs532377395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42226886 | AGAAGGCTCGAAGGC[A/G]CCGCGGGCTGGGGTC | 10138 |
rs532387496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42236411 | AATATGAAAAATGTA[C/T]GAAATATTTTATCAA | 10138 |
rs532409523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233605 | CAACCTCGAACTCTG[A/G]GGCTCAAGGGATCCT | 10138 |
rs532487367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42169702 | AGAGGTGTGAACCAC[C/T]GTGCCCAGCCAACTT | 10138 |
rs532498916 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42189121 | TGAAAAGCAGGGCAA[G/T]TAAGGTAGAGAGAGC | 10138 |
rs532562273 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42182238 | TGTTTGACGAGGAAG[C/G]AGAAGGCATGAAATT | 10138 |
rs532783565 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42211472 | CCAGGCACAGTGGCT[C/G]ACGCCTGTAATCCCA | 10138 |
rs532855989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42204775 | ACATATGCTACAATG[C/T]GGATAAACCTTAAAC | 10138 |
rs532904752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42173876 | CAGAGAAAAGAGAAG[C/T]TATTCGATTAGAATG | 10138 |
rs532924972 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42167145 | GGCCTGTTGGGGAGT[C/G]GGGGGAAAGGGGAGG | 10138 |
rs533113136 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42196570 | TGCAAGTTGAATTAT[C/G]TACAGAGACTAAATA | 10138 |
rs533132014 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42157012 | ACATCAAGTCCTTAA[A/G]AGATTCTGGAAAAGA | 10138 |
rs533137412 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42159413 | CAACATAAAACTCTT[C/T]AAATAGTTGTAAACA | 10138 |
rs533139240 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42201086 | TGATAATAGCCTAAA[A/T]ATAGATGTAGGTAAT | 10138 |
rs533161644 | in-del | -/AAAG | | | intron-variant | YAF2 | GRCh38.p7 | 12:42171516 | TTTAAATTAAAAAAA[-/AAAG]AAAGAAAGAAAGAAA | 10138 |
rs533167728 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157672 | ATTATCCACTATCAT[C/T]TTAGGAAAGCATTTA | 10138 |
rs533179540 | snp | A/G | | | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42161299 | TGCAATTATCTGTTC[A/G]GTATGTTGAAAACCA | 10138 |
rs533228924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42193696 | TTTTGTGGAGACAGG[A/G]TTTTGCCCTGTTGCC | 10138 |
rs533231374 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42195941 | AGAATGGGAGGACAG[A/G]CCAGGCACAGTGGCT | 10138 |
rs533262208 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42204409 | TCTACTATGTACAGA[A/C]TTTTTTCCCTTGTCA | 10138 |
rs533282742 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42200167 | CACTCTGGTAGTTTC[C/G]TAAAATAATAGAAGT | 10138 |
rs533300290 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42225511 | GATTTTATGGTTTTA[A/G]GTCTTATGTTAAAGT | 10138 |
rs533307873 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42190669 | GTATCCTGTATGTTA[C/T]TCATGTCTTTCATTT | 10138 |
rs533320471 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | YAF2 | GRCh38.p7 | 12:42190340 | CAGAGTGAGTGCAAC[C/T]GTCTCAAAAAAATAA | 10138 |
rs533324993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42186367 | CTCAAAATAAATAAA[C/T]AAATAAACAAAAATA | 10138 |
rs533333280 | in-del | -/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42230477 | ACTAATAGGACTCAA[-/T]TTTTTTTTTTAAATA | 10138 |
rs533402180 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42230737 | CTGAGGTTCCAGAAA[A/C/G]GAGTTTATGCCACAT | 10138 |
rs533414188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42223630 | CCTGTAAAAGTGCTG[A/G]GATTACAGGTGTGAG | 10138 |
rs533422441 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | YAF2 | GRCh38.p7 | 12:42194652 | TTCTTATATATCTAA[-/T]TTATGTCCTATAATA | 10138 |
rs533443345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42201802 | GTCTTGCACTCCTGA[C/T]CTCAAGTGAACCATC | 10138 |
rs533446616 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42179660 | CAGGCGTGGTGGCAC[A/G]TGCCACCCAGCTACT | 10138 |
rs533507237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42177199 | TCTCTATGTGATATA[A/G]GCTCTTCCTATCTGA | 10138 |
rs533531355 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42194827 | AACATGCAAACATAC[A/G]TAAGTTCAATTTTGC | 10138 |
rs533595347 | snp | A/C | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233624 | TCAAGGGATCCTCCC[A/C]CTTCAGCCTCCTGAG | 10138 |
rs533613504 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | YAF2 | GRCh38.p7 | 12:42211772 | AAAAAAAGTCAGCCA[A/G]GCACGGTGGCTTGCA | 10138 |
rs533669025 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42162899 | CTTAAAAAATAGGAC[G/T]GACATAGAGTTTGAG | 10138 |
rs533746512 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42230552 | AGATCATGTTAGTAG[A/C]ATTCCAAAGGAGAGA | 10138 |
rs533823173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42213198 | AAAAGAGAAGCCCAC[A/G]TAGCAATAAACTGAT | 10138 |
rs533827554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42220766 | CATGTAAAGATGAAA[C/T]TGTTTAATTCATATG | 10138 |
rs533891413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42214033 | GTCCATTCTCCTTAC[A/G]GAAGCCACAGAGCAC | 10138 |
rs533959625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42212248 | GAAAAAAATCTCTCC[A/G]AAAGAAATTTATCTT | 10138 |
rs534083458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42207637 | GTGGCTCATGCCTGT[A/G]ATCCCAGCACTTTGG | 10138 |
rs534097419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42200501 | AAATGAAGATTAAAA[C/T]AACAAAGGTCAATCT | 10138 |
rs534130924 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | YAF2 | GRCh38.p7 | 12:42169501 | TCACTGCAGCCTCTG[C/T]CTCCTGGGCTCAAGC | 10138 |
rs534146353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42169169 | TAAGGTCACCAAGTA[C/T]GCCAAAACCAAAAGA | 10138 |
rs534148012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42160939 | TACATGTATTTAAGG[C/T]AATTTATGTGTAACT | 10138 |
rs534184566 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42161542 | ACTTTGTGTATATTA[G/T]TATGTCAAGGTTAAA | 10138 |
rs534193692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42236080 | GAACAACAAAAAGCA[A/G]TAATATATAGTACCA | 10138 |
rs534354031 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42190648 | TTCTTAGAAATAATT[G/T]TATTTGTATCCTGTA | 10138 |
rs534411140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42188542 | AGGCATGCACTACCA[C/T]GCCCACTAATTTTTA | 10138 |
rs534440156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42198439 | AAAATACAAAAATTG[A/G]CCAAGTGTTGATGGC | 10138 |
rs534496533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42191433 | CATTTACTTCCAATC[C/T]CCCTAGTAATTTTGT | 10138 |
rs534499721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233935 | CAGCACTTTGGGAAG[C/T]CGACGCAGACGGATC | 10138 |
rs534507266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42183052 | TTTCGTTATTATTAT[A/G]TCTGTTATGGTGATC | 10138 |
rs534555683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42225864 | TTGGGTATACAGGCT[C/T]TTTTTTGGTTCCACA | 10138 |
rs534559989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42218392 | AAATGTTATATCTTC[A/G]TGACTGTTGTTAGTA | 10138 |
rs534572168 | in-del | -/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42167154 | GGGAGTGGGGGGAAA[-/G]GGGAGGGAGAGTATT | 10138 |
rs534603424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42175511 | ATGTTTTATGTGTGG[C/T]TTATTGTATGTCAAT | 10138 |
rs534619405 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42219063 | GGGCAGTGATTTTCC[A/G]AAAATGTTTTGCAAA | 10138 |
rs534629626 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157902 | TGGGATTACTGGCAT[A/G]AGCCATCACACCCGG | 10138 |
rs534715942 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42231752 | CCACTAATCTTCTCA[G/T]AAAAGTCTTTATACA | 10138 |
rs534730553 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42181569 | AGTCTATTGTATGCT[C/G]TACAGGTAGCCTGGT | 10138 |
rs534782571 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42173328 | TCCCCCAACTCCTGG[A/C]AGGTGGTACCAGGAA | 10138 |
rs534839211 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42176840 | GGCGTGGTGCTGGGC[A/G]TCTGTAATCCCAGCT | 10138 |
rs534840584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42184582 | CTCAAAGTGCCGGGA[C/T]TACAGGCATGAACCA | 10138 |
rs534892731 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42219859 | CTAACAAGCTCCCAG[A/G]TGATGCTAACGCCAC | 10138 |
rs534930285 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42200807 | AAAGGTAGCATGGTA[G/T]AGTGGACTCTGAAGC | 10138 |
rs534942182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42168296 | TGATTCTCCTGCCTC[A/G]GCCTCTCTAGTAGCT | 10138 |
rs535008458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42195586 | CACATAGGCTCAGAA[C/T]TAATGATTATTAAAA | 10138 |
rs535031073 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42158052 | AAACAGAGAAAAACA[C/T]GTACCCTAAACCTAG | 10138 |
rs535048888 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42159916 | TATTGTTTACTAGTC[C/T]GCTAGTAAACATTAC | 10138 |
rs535061675 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42223806 | CGCATGTTCTCACTC[A/G]TAAGTGGGAGTTGAA | 10138 |
rs535073261 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42216279 | TACGCAAAAGTATTA[A/T]CTTGTTACAACTTAA | 10138 |
rs535087710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42214821 | CCAGCCGGGCCAACA[C/T]GGCGAAACCCCTTCT | 10138 |
rs535092865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42224459 | GGTATACACGTGCCA[C/T]AGTGGTTTGCTGCAT | 10138 |
rs535167228 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42223771 | TCAGCAAACTAACAC[A/G]GGAACAGAAAACCTA | 10138 |
rs535355659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42230213 | AGTGAGCCAAGATCG[C/T]GCTACTGCACTCCAG | 10138 |
rs535398915 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42179295 | GCCAACGTGGTGAAA[C/G]CCCGTCTCTACTAAA | 10138 |
rs535406803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42172323 | ACAAAATTATAAATT[A/G]TTATAATTTGAAATC | 10138 |
rs535494863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42207870 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCT | 10138 |
rs535503349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42200724 | GTAAATTAGATCACA[C/T]TGTACACATCATTCT | 10138 |
rs535550792 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42192460 | GCTGCAGTGAGCTGT[C/G]ATCGTGCCACTGCAC | 10138 |
rs535561356 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42193093 | CCGAGGGGGGGCAGA[A/T]CACTAGAGGCCAGGA | 10138 |
rs535592428 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42184719 | CTTCTGGAAAGGCTT[C/T]GCCATTCTAGATGTC | 10138 |
rs535607121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42236943 | TACAATAAATAAAGT[C/T]TGAAAATAGGCAGAG | 10138 |
rs535660983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42221221 | AATTATAAGAAGAAA[C/T]CTTTAAGAAGTTACT | 10138 |
rs535684156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42202009 | AAAGTTGCATACTCA[C/T]CTATACTATCCTCTT | 10138 |
rs535719681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42221892 | TCTTCCCTCTGAAGA[C/T]GCTCTTATCTGTCTA | 10138 |
rs535747079 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42194749 | CTAAATACTACCTAT[G/T]GTCCAGGCCCTACAT | 10138 |
rs535748938 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42220214 | ACATTTTAGAAGTAG[C/G]TAACTTCTGACTGGA | 10138 |
rs535750359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42186674 | AAAAGCAAGACTCCA[C/T]CTCAAAAAGGAAAAA | 10138 |
rs535799950 | in-del | -/ACA | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42168108 | TTACACTTTTGTCTC[-/ACA]ACATAACTCCCACAA | 10138 |
rs535828271 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | YAF2 | GRCh38.p7 | 12:42183025 | GTCGCATTTTGGTAA[C/T]TCATAAAATGTTTTC | 10138 |
rs535896406 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42162595 | AGATAAAAATACATT[C/T]TAACAGATGCTCTAC | 10138 |
rs535936559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42176547 | AAGCAGTATTTATTC[C/T]GTTTTTCCTCTCATA | 10138 |
rs535952719 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | YAF2 | GRCh38.p7 | 12:42230235 | GCACTCCAGCCTGGC[A/G]ACAGAGCAAGACTCC | 10138 |
rs535970837 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42169292 | TTCCTCTTCCTACCT[C/T]CTCCAGTAAGTAGGT | 10138 |
rs535973068 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42176913 | GGGAGGTTGCAGTGA[A/T]CCGAGATCACGCCAT | 10138 |
rs536018216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42185401 | AATATTACATAAACT[C/T]AATTGATAAAGAAGC | 10138 |
rs536043056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42237798 | GCCCGGGCCCCGCGG[C/T]CGCCCCCGCCCCGCC | 10138 |
rs536106534 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42212998 | AGTGATAAAACAGAT[C/T]AAGGAGCAATAATGC | 10138 |
rs536147988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42170923 | TCCCCTAATATCCGC[C/T]CTAAATGTTGAATGG | 10138 |
rs536164545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42198643 | TCTAAAGAAATTAAG[C/T]AGATCTAGGTATCAG | 10138 |
rs536185582 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42171381 | TAGTCCCAGTCACTC[A/C]GGAGGCTGAGGCAGG | 10138 |
rs536267857 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42171534 | AGAAAGAAAGAAAGA[A/G]ATATGTTACTTGTAG | 10138 |
rs536314629 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42219270 | GGACAGCCAGGTCTC[A/G]TCTACCCCAAAAAGT | 10138 |
rs536391780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42160887 | AAATTTCTGAGCATA[C/T]AATAAATAATAAAAG | 10138 |
rs536413098 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42161900 | TCCTCATATGTAAGG[C/T]AATTTAAATATACAA | 10138 |
rs536423004 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42206933 | ATACCTTCTACCCAG[A/T]TTCAAAATTGTTAAC | 10138 |
rs536433433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42212505 | GAAACAAAGAAAGTG[C/T]ATAGTTTTTCCTTTA | 10138 |
rs536450961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42204462 | TAACAACTATTTACA[C/T]AGCACTTGGGTTATA | 10138 |
rs536571650 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42206611 | AAGACTCCATATTAA[A/C]AAAAAAAAAAAAGTA | 10138 |
rs536620749 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42167481 | ACCTCAAGGAAAGAA[A/C]AAAACATAAAGTATC | 10138 |
rs536627053 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42181016 | GTGCCCATAATGGGA[A/G/T]GATGGCTTCTTTGAT | 10138 |
rs536637678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42217767 | TATAAAATATCTTCA[A/G]TACACTGTGTAAATA | 10138 |
rs536659132 | snp | G/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160173 | GTTGTTCTTTGACTT[G/T]TATACATATAACTAT | 10138 |
rs536678910 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42195002 | ATCTTCTAAACTCCA[A/G]TATTAGTTAAAATAT | 10138 |
rs536681932 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42202629 | AGTATTTCAATCTAA[A/T]TAGCATAACTTTTAT | 10138 |
rs536762893 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42204316 | GGTATATATAGTCAG[C/G]GCTCCATATCCATGG | 10138 |
rs536792708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42179714 | GCTTGAGCCCAGGAG[A/G]TTGAGGCTGCAGTGA | 10138 |
rs536845353 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42208485 | TTAAAAATAGCAATA[C/T]AACCTAAAGCTAATA | 10138 |
rs536854750 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42224578 | TTCCCCTCCCTGTGT[C/G]CATGTGTTCTTATTG | 10138 |
rs536856549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232988 | TAAAGCGGTTCTAAT[C/T]TGCAAAACTGTAAAA | 10138 |
rs536881873 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | YAF2 | GRCh38.p7 | 12:42197058 | CCTCAGTAAATGTTT[A/G]GTGATGAGCTTAAAA | 10138 |
rs536915632 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42209669 | CAAATATGACATCTG[A/C]ATAAATTTTACAATA | 10138 |
rs536922308 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42225146 | GAGTTTTTCACATTT[G/T]TTGGCTGCATAAATG | 10138 |
rs536942477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42197618 | TGGAATAGAGGTGGT[A/G]TAACAAAGAGGTAGG | 10138 |
rs536977190 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234434 | ATTTGGGTAATGGGT[A/C]CACTGGAATCCCAAT | 10138 |
rs537044262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42175643 | GCACTATGGGAGGCC[A/G]AGGTGGGCAGATCAT | 10138 |
rs537047771 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | YAF2 | GRCh38.p7 | 12:42169578 | CCACCACACCGGGCT[-/A]AATTTTTGTATTTTT | 10138 |
rs537144228 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | YAF2 | GRCh38.p7 | 12:42195438 | TATTACCAGAATTTA[A/G]AGAAGGAAAAGGTAA | 10138 |
rs537180194 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42179909 | CTGATAGTATACTCA[C/T]TAATAAACCATGCCT | 10138 |
rs537216954 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42173217 | CTTTCTCAGCCTCTT[G/T]AGCAGCTAAGACTAT | 10138 |
rs537257642 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42219677 | CTTTGGAAAAGGCAG[C/G]TCAAAGTGGGATGAA | 10138 |
rs537336350 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42181496 | GAATAACTGCTCCGG[C/G]AACAGCTTACTGCAG | 10138 |
rs537368656 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | YAF2 | GRCh38.p7 | 12:42209545 | CTCTAGCCTGGGCGA[C/T]AGAGCCAGACTTTGT | 10138 |
rs537421491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42186064 | GGCATGGTGGTACAT[A/G]CCTATAATCCCAGCT | 10138 |
rs537422987 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42167360 | CTATCTCAAGATATA[A/G]GAAAAAATCAAATAA | 10138 |
rs537428633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42220904 | AATATTTGTATCACA[A/G]ATAAAAGAGAGAAAT | 10138 |
rs537439598 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238770 | TCCTTAGCTACCCAG[C/T]CCCCGCCTGCAGTAT | 10138 |
rs537449010 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | YAF2 | GRCh38.p7 | 12:42163882 | AAAGCCCTTCTATCT[C/G]CAGGTATCTTAAGGT | 10138 |
rs537485987 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42198105 | GAGTGAAATGTTGGG[C/G]CTCACCTTATAAAAA | 10138 |
rs537499620 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42185285 | TTTCACAGATGAGGA[A/G]TTGCTTATTACAGAT | 10138 |
rs537586676 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42217025 | CCATCTGGCATTCCC[A/C]TTGTTCAGGACATTA | 10138 |
rs537637773 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42156676 | TTTTTATCACCCTCA[A/G]TGGCCAGGGAGGGCA | 10138 |
rs537638881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42223718 | GGATGAGTTCATGTC[C/T]TTCGCAGGGACATGG | 10138 |
rs537742659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42193218 | TACTCGGGAGGCTGA[A/G]GCAGGCGAATCACTT | 10138 |
rs537794521 | snp | C/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42158096 | CGCATATTTTAACGT[C/G]AGTTCTGTTTATGGA | 10138 |
rs537819811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42201598 | TTGTTGCTGTTGCTG[C/T]TGTTGTTGTTGAGCC | 10138 |
rs537906930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42214713 | TGCAACTTAAATTCC[A/G]TGAGAGCTGGCCAGG | 10138 |
rs537958820 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42191539 | AGCTATATCATGGGG[A/C]CTTTATACTTTTAAC | 10138 |
rs537960021 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | YAF2 | GRCh38.p7 | 12:42207668 | GAGGCCGAGGCGGGC[A/G]GATCACAAGGTCAGG | 10138 |
rs537989128 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42164807 | AAGCGTGGTGGCTCA[C/T]ACCTGTAATCCCAGC | 10138 |
rs538047571 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42236224 | AAATATACTCTAAAC[A/C]AACTCCAACCTTACA | 10138 |
rs538176708 | snp | A/G | 3.20436e-05 | 0.00400259 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238203 | CTATCACCGCACGCC[A/G]AGAGTCGCCGCCGCG | 10138 |
rs538214092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42189516 | CAAGGAGAACCATTA[A/G]GGGCCTGAGAGCATG | 10138 |
rs538225009 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42162706 | GTTCCTCTATGGCAA[C/G]ACAACATAAAAAATA | 10138 |
rs538314749 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42206346 | GGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 10138 |
rs538343171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42182397 | AATCAATCAGCTTGT[C/T]ATGTAATTACAGACA | 10138 |
rs538399700 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42183733 | GTTATACAGAAGATC[G/T]AGCTAAGAGAGTTGA | 10138 |
rs538401171 | snp | A/C | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239431 | AATTCATTCCCTTAC[A/C]AGAACCCTTCCTTCA | 10138 |
rs538420557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42176427 | TGCCCAACCAACAAT[A/G]TACTCTTGATTTCTC | 10138 |
rs538535111 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42184571 | CACCGCAGCCTCTCA[A/T]AGTGCCGGGATTACA | 10138 |
rs538563638 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42212923 | CTAGGTAACTCTGCT[A/G]GTTTACTAGACTCCT | 10138 |
rs538563691 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42205162 | AATTTGAAAAAAAAA[A/T]TCACTAGAAAATAAA | 10138 |
rs538597494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42162733 | AATAATGAGAAAATA[C/T]TGTACAATCTAAGAA | 10138 |
rs538669380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42174747 | TTTCGACCCTGGCTC[C/T]ACATTGGATTTCACT | 10138 |
rs538695071 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42225107 | CATTGTGGTTTGATG[G/T]GCATTTCTCTAATGA | 10138 |
rs538773483 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42202156 | TTTTCTCTCCCTCCC[A/G]CCAAGGAATGCCATT | 10138 |
rs538795537 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42159028 | TCATTTAACAACACT[A/G]AAGAATGAGGTATAT | 10138 |
rs538796463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42168434 | TGATCCACCTGCCTC[A/G]GCCTACCAAAGTGCT | 10138 |
rs538803051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42167426 | GGACCAAAAGGTCCA[C/T]ATGGTAATTTCAAAA | 10138 |
rs538812771 | in-del | -/TTT | | | intron-variant | YAF2 | GRCh38.p7 | 12:42236327 | CATTTTAGCAAATAC[-/TTT]TTTTCTTTTTGGAAT | 10138 |
rs538832286 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42159980 | AAAAACCTCAAAAAA[C/T]AGATAAAACCAGAAA | 10138 |
rs538857427 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | YAF2 | GRCh38.p7 | 12:42223765 | TCATTCTCAGCAAAC[C/T]AACACGGGAACAGAA | 10138 |
rs538951971 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42188740 | CACATGTACAATTTT[A/G]TTATGTAATAACCTA | 10138 |
rs538995613 | snp | G/T | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42174040 | TTAAACAATATTTCC[G/T]TCTCTACTGGGTTAT | 10138 |
rs539001021 | in-del | -/AAGAGAAGAAAGAG | 0.0217236 | 0.101931 | intron-variant | YAF2 | GRCh38.p7 | 12:42230266 | TCAAGAAAGAAAAGA[-/AAGAGAAGAAAGAG]AAGAGAAGAAAGAGA | 10138 |
rs539010122 | snp | A/G | | | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42210094 | TGAGTCAGCAAGCCC[A/G]GCCAACTAAATGTAT | 10138 |
rs539045260 | in-del | -/TATAA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42224282 | CAGTAAGCATGTATT[-/TATAA]TATATTTTAGTTTCT | 10138 |
rs539089290 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42209821 | TTTGTTTTTTGAGAC[A/T]GAGTTTCGCTCTTGT | 10138 |
rs539224454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42195393 | ATACAGGAAACAAAT[A/G]CCAAATACTAAAACA | 10138 |
rs539236812 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239871 | ACAAAAATTAGCCAG[C/T]TGTGGTGGCGGGCGC | 10138 |
rs539252561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42203600 | TTTTTAAAACTTTAA[C/T]GGGTATTGAGTTTTA | 10138 |
rs539310424 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42196199 | GCCACTGCACTCCAG[A/C]CTGGGCGACAGAGCA | 10138 |
rs539405191 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42165820 | TAACTCCTCATCAAC[A/T]GTCATGCCTAATCCT | 10138 |
rs539411381 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42193167 | TAAAAATACAAAAAT[G/T]AGCCGGGTGTGGTGG | 10138 |
rs539441152 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42222864 | AGTGGCTGACACACA[C/G]TAAGTGCTCTGTAAG | 10138 |
rs539443326 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157961 | TAAGGTAATAAATGC[A/T]GGAAAACATCCAAAT | 10138 |
rs539523857 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42185448 | ACTGGCTTAAATTTT[G/T]AAAGAAGTTTTGCTG | 10138 |
rs539577198 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42165972 | ACCCAGGCTGGAGTG[C/T]GGTGGCGTGATCTTG | 10138 |
rs539620066 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42171461 | TACCTCTGAATAGCC[A/T]CTGGCATTTCAGACT | 10138 |
rs539620219 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42222232 | TACCTTAAAGAAAAA[A/C]ACACTAAGGTTTCAC | 10138 |
rs539664781 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42196857 | AGCAAACCGATACCA[C/T]CAGTCATTTGATCCT | 10138 |
rs539665139 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42163048 | CCAAGAAGGCTTGTT[A/T]AGCTTGCTTAGCCCT | 10138 |
rs539681995 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42231871 | GTGTTTTCCTTGAAG[G/T]GATATATTTTTTGAA | 10138 |
rs539695525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42215346 | GAGGCTGAGGTGGAT[C/T]GCAAGAGCCCAGGAG | 10138 |
rs539718739 | in-del | -/AAGAAAGAG/AAGAAAGAGAAGAAAGAG | 0.0227355 | 0.104344 | intron-variant | YAF2 | GRCh38.p7 | 12:42230271 | AAAGAAAAGAAAGAG[-/AAGAAAGAG/AAGAAAGAGAAGAAAGAG]AAGAAAGAGAAGAAA | 10138 |
rs539721657 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42187502 | ACAAAAATTAGTGGT[A/G]TGCTTCTATATTCTT | 10138 |
rs539742174 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42180169 | AACCCCTTCCCTACA[G/T]GTGGGCTGGACCTAG | 10138 |
rs539759872 | in-del | -/AC | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42199723 | TAGCACTAACCAAAG[-/AC]ACAGAATACGGTAAT | 10138 |
rs539814639 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42161298 | ATGCAATTATCTGTT[C/G]GGTATGTTGAAAACC | 10138 |
rs539829787 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233877 | TTCTTGCCTTATAAG[A/G]ATCTTCAGATAGGCT | 10138 |
rs539844234 | snp | C/G | 0.0433465 | 0.140692 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42237905 | GAAGAGGCAGGGCGC[C/G]AGCGCGGCCGCAGTC | 10138 |
rs539846937 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42164868 | TGAGTCCAGGAGTTC[A/G]AGGCCAGCCTGGGCA | 10138 |
rs539854100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42202407 | CAGGAGGCTCCCTCA[C/T]GATCCTTACCAATCA | 10138 |
rs539870692 | in-del | -/TT | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42187871 | AAGTCATAAAAGACA[-/TT]GTGACTTTCATCCTG | 10138 |
rs539899145 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | YAF2 | GRCh38.p7 | 12:42205347 | AGCTTTGACTGATCA[C/T]GACATTGTTTTTCTT | 10138 |
rs539907615 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238604 | TCTGAGGAGGAAAAC[A/G]TCTGTCCCACCGACT | 10138 |
rs539939856 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42172383 | AAGCCACAATGACAG[C/T]ATGTACCATCAGCAG | 10138 |
rs539966075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42198079 | TAGGGAAAGCATATC[C/T]AATCCCCATAGAGTG | 10138 |
rs539975414 | in-del | -/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42188384 | TATATATATTTTGCT[-/T]TTTTTTTTTTTTTTT | 10138 |
rs540001118 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42230101 | GTCTCTACTAAAAAT[A/T]AAAAAATTAGCTAGG | 10138 |
rs540044241 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42221911 | CTTATCTGTCTATCA[C/T]TAAGGTTTCAAGTAA | 10138 |
rs540065546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42191074 | ATCAGACAGGCAAAT[C/T]ATATGACTCAGATTC | 10138 |
rs540127269 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42191778 | GGTTTTAACAGGAGT[C/G]GGGGTGAATAAGAAT | 10138 |
rs540160008 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42183938 | GTGAAGCCAATGCTC[A/T]CTGACCATTCCAAAA | 10138 |
rs540170772 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42226473 | TCGAGACCAGACTGG[A/G]CAACATAGGGAGACA | 10138 |
rs540210209 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42219455 | AGAGATAGGAGGTAT[A/G]ACAGAGAAAGCATTT | 10138 |
rs540274637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42212561 | ACTGAATAAATGAAA[A/G]AAAACAAAACAAACA | 10138 |
rs540333823 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42224624 | TGAGTGAGAATACGT[A/G]GTGTTTGGTTTTCTG | 10138 |
rs540336545 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42206091 | TTTTTCTGCATTTCT[C/G/T]TGTGCTTGTCCGGAG | 10138 |
rs540433171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42182636 | AACCTCAGTATGTAA[C/T]TGGCAATCAAAAATA | 10138 |
rs540471697 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42226228 | CTTCGTTTTTAGCTA[A/T]ATTATATCATATAAA | 10138 |
rs540675236 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232358 | CCTCATAGAAAGCTT[A/C]AACTAAAAAGATCTC | 10138 |
rs540694437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42216677 | ACAAATGACTATCAA[A/G]TATGTATTTACAGCC | 10138 |
rs540732334 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YAF2 | GRCh38.p7 | 12:42190014 | TGTTTTAATATATTA[C/T]ACAATGCCATAACAA | 10138 |
rs540745200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42182132 | TCACAAAAAAAGAAG[A/G]TTAAAACTACAAAAG | 10138 |
rs540782625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42174209 | TATACTCACTCTATA[C/T]TTTTCCCACTCTCTC | 10138 |
rs540782944 | in-del | -/TATTTTTG | 0.00914312 | 0.0669923 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42158391 | AACTGTTACAAAAAA[-/TATTTTTG]TATTTTTGTAATGGG | 10138 |
rs540808857 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42225643 | ATAGGGAATCCTTTC[C/T]CCAGTGTTTGTTTTT | 10138 |
rs540844482 | in-del | -/TA | 0.00318978 | 0.0398085 | intron-variant | YAF2 | GRCh38.p7 | 12:42170672 | AAACAAACAAAAAAC[-/TA]TATACACACACACAC | 10138 |
rs540919640 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42210869 | GAAATCATTAGAATG[C/G]TTTCATTTTAAAAAG | 10138 |
rs540979351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42165032 | TGCATTCCACCCTGG[A/G]TGACAGAGTGAGACC | 10138 |
rs540984233 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42180298 | CCCTTGTTGTGATCT[C/T]CCCTAACAGAGTGGC | 10138 |
rs541046382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42215034 | TAAATAAATAAATGA[A/G]TTCCATGAGAGTAAA | 10138 |
rs541105741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42207763 | GGGCGTCGTGGCGGG[C/T]GCCTGTAGTCCCAGC | 10138 |
rs541141541 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42166155 | CAACCTCAGGTGATC[C/T]GCCTGTCTTGGCCTC | 10138 |
rs541154802 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42156981 | TACCAATGACTTACT[A/C]AATAGCTCAGTTCCT | 10138 |
rs541198671 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42226711 | TTATACCTACAACTT[-/A]AGAGACAAAATAGTC | 10138 |
rs541258636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42210026 | TGTTCTCGAACTCCC[A/G]ACCTCAGGTGATCCA | 10138 |
rs541271043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42203342 | GAATTATTTTATTAA[C/T]ACAAACAGTACTTTC | 10138 |
rs541280791 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239199 | ACAGCCATCTAACTG[C/G]TCTCCGAAGCTCCAC | 10138 |
rs541314891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42195059 | TAGATACGGTTTCAG[C/T]CCTTACAGTTCAGCG | 10138 |
rs541322378 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42167597 | TTAAAACAATACACA[C/T]ATCCTGTAACTAATT | 10138 |
rs541322418 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42159239 | AAATGTTATCATGAT[A/G]TCTTATGTGATATTT | 10138 |
rs541325484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42186943 | CCAATTCAGCGAACT[A/G]TAATTTTAAATTAGC | 10138 |
rs541331462 | snp | C/G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42209230 | GAAGTTCAAGATACA[C/G/T]TGAAAACTGTCATTA | 10138 |
rs541348983 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42186296 | GAGGCGGAGGTTACA[C/G]TGAGTCAAGATGGTG | 10138 |
rs541352744 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42195867 | ATTGAAATGAATAGA[A/G]ATTAACTAAACTGGT | 10138 |
rs541362323 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42214541 | CCTCCCAAAGTGCTG[A/G]GATTACAGGTGTGAG | 10138 |
rs541363317 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160394 | CTGCAGAGACCAAAA[A/T]GTTAAGTCTGGAAAT | 10138 |
rs541416028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42223210 | AGGTTTCTTTGCTTA[C/T]TCCTCTTTCCTTCAA | 10138 |
rs541417059 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42158686 | TAGAAAGATGAGTAT[C/T]TTCCCACCTATGTAG | 10138 |
rs541418669 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42217791 | GTAAATATATCATCA[C/T]TTTTAGCAAAGAATT | 10138 |
rs541589291 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, synonymous-codon | YAF2 | GRCh38.p7 | 12:42237418 | CCTCTTCAATTACCC[C/T]TCACCGCAAACCATC | 10138 |
rs541723897 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42213883 | ACAGGGGTACTACAC[A/T]GACCTCCATTTCTAA | 10138 |
rs541734512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42171676 | ATCTCATATCTGGCT[A/G]GGCGTGGTAGCTCAC | 10138 |
rs541737304 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42240023 | CCTCTAAGTAAATAA[A/G]TAAATAACATTTTTT | 10138 |
rs541795560 | in-del | -/A | 0.426738 | 0.176816 | intron-variant | YAF2 | GRCh38.p7 | 12:42171513 | TCTCTTTAAATTAAA[-/A]AAAAAAGAAAGAAAG | 10138 |
rs541824711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42226760 | CATAGTGTTCAAAAT[C/T]ATTGGAAAAGCAACG | 10138 |
rs541852369 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42235566 | AAGAGAAGAGAATTC[A/C]GAGAGAGGAAGGAAG | 10138 |
rs541887884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42227567 | GCGTCTCTGCCCGGC[C/T]GCCCTGTCTGAGAAG | 10138 |
rs541887923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42219568 | TGCCCACATACTCAC[A/G]TTCCTGTACACATAT | 10138 |
rs541897712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42183172 | TGTTTGTGTTCTGGC[C/T]GCTCCACTGACCAGC | 10138 |
rs541986244 | snp | C/T | | | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42210044 | CTCAGGTGATCCACC[C/T]GCCTTGGCCTCCAAA | 10138 |
rs541998950 | snp | G/T | 0.00795532 | 0.062565 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238361 | AGCTGTCGGGGAAAC[G/T]CCTGCCTGGGCGCAC | 10138 |
rs542011031 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | YAF2 | GRCh38.p7 | 12:42229854 | ATCATTTTATGGGAC[C/T]GTATATGTGGTCCCC | 10138 |
rs542037900 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | YAF2 | GRCh38.p7 | 12:42228041 | GTCAGCCCTCCGCCC[A/G]GCCAGCCGCCCCGTC | 10138 |
rs542043727 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42185700 | TTGAATTTTTTAGCT[A/G]TATTTTAAATTAAGG | 10138 |
rs542082791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42178614 | TTGCTCCCATTTTCA[C/T]TTTTATTTTTTAAAA | 10138 |
rs542098041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42213429 | ATCTGACCAGATTTT[A/G]AAGCCTTACCTTACT | 10138 |
rs542113675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42222441 | CAACCCAGGTTTCAA[C/T]CTAGGCTCTAACATT | 10138 |
rs542147367 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42163171 | GACCACACTTTAAAA[A/G]AAAGCTTGAGGAAAT | 10138 |
rs542163917 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42186214 | AAAAAAAAAAAAAGG[C/T]TGGGCTTGGTGGCTC | 10138 |
rs542169451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42175858 | GATGTGTATTCAAGG[C/T]TGAAAACAATTGATC | 10138 |
rs542171397 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42167764 | TAATCCCAGCACTTT[G/T]GGAGGCCAACGCGGG | 10138 |
rs542202076 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | YAF2 | GRCh38.p7 | 12:42184467 | GGCATGTGCCACCAC[A/G]CCTGGCTAATTTTTA | 10138 |
rs542211557 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42236239 | CAACTCCAACCTTAC[A/C]CAGCCAAGAAGATAC | 10138 |
rs542246248 | in-del | -/C | 0.00478085 | 0.0486577 | intron-variant | YAF2 | GRCh38.p7 | 12:42228030 | GAGGTGGGGGGTCAG[-/C]CCCTCCGCCCGGCCA | 10138 |
rs542260533 | in-del | -/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42227397 | CTAGGAAGTGAGGAG[-/C]GCCTCTTCCCAGCCG | 10138 |
rs542287551 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42207808 | AGGCAGGAGAATGGC[A/G]TGAACCCAGGAGGCA | 10138 |
rs542308043 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42168489 | GCCTGGCCGAAAGAC[A/T]GAAATTTTATGTCAT | 10138 |
rs542388587 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42161155 | GAAATAGTTGCACCA[C/T]GGAGGAAGGTGATAA | 10138 |
rs542393327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42170190 | TTATGTGTTTTTGAT[A/G]AGTCAGTCAGTCACA | 10138 |
rs542398062 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42204529 | ATATGGGAGAATATG[A/C]ATAGGTTATATGCAA | 10138 |
rs542473497 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42197942 | GTCACATATGTTATA[A/C]CTTGGTATACCAAAC | 10138 |
rs542480294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42214347 | CACAATCTCAGCTCA[C/T]TGCAACCTCCCCTTC | 10138 |
rs542523319 | in-del | -/CATCT | | | intron-variant | YAF2 | GRCh38.p7 | 12:42203381 | AATATTTCTAGGGAG[-/CATCT]CATCTCATCTCATTT | 10138 |
rs542617663 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42211277 | ACTGAAAATACAAAA[A/T]TTAGATGGACATGGT | 10138 |
rs542641104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42226168 | ATATTTCTTAATACG[C/T]TGTACACTTTCACAG | 10138 |
rs542672899 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42201831 | TCTGCCTTGGTCTCC[C/G]CAGATTGATGGCATT | 10138 |
rs542868982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42190181 | GACCACATCTCTACA[A/G]AAAATTTTAGAAATG | 10138 |
rs542909905 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42198844 | ACACCAAAGTTTTCT[C/T]AAATGCTCTAAGTCT | 10138 |
rs542929956 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42175233 | TCAAGAGGAGTTATG[A/C]CGAGTGAAAGAGATT | 10138 |
rs542930798 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42181971 | TAGTGGCCAGTGTTA[A/C]CTAGTGTAATCTTTT | 10138 |
rs543031244 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42202332 | ACAGCTTGACCTTTA[A/T]ATACATATACTCCTG | 10138 |
rs543033840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42230436 | CTTGAACACTATCCT[A/G]AGGATCTCAGCCTTT | 10138 |
rs543092752 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42203068 | AGGTCATTTTCCACA[A/C]AAAAAAAAAAAAATC | 10138 |
rs543104885 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42195763 | GGTGTGTTGAGACTG[C/G]GTTAAATTCAGGCAG | 10138 |
rs543112121 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42174704 | ACCTCATTCAGTCCT[C/T]GGTTTTAAGTATCAT | 10138 |
rs543131790 | in-del | -/GGTTGGGAGT | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42211523 | AGGTGGATCACCTGA[-/GGTTGGGAGT]TCAAGACCAGCCTGA | 10138 |
rs543139957 | in-del | -/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42235524 | GAGAAATTAGAGCTC[-/T]TAGGTTTAACTTAGA | 10138 |
rs543147874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42231375 | GCATTCAATTTGTTG[C/T]AATATGTTGTTTTGG | 10138 |
rs543163455 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42196340 | CCTATAAGTGGGTGG[A/C]AAATATGGCTGGGAC | 10138 |
rs543188168 | in-del | -/CTTCA | 0.0130921 | 0.0798413 | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42156604 | CTTTTTCCCCTTCTT[-/CTTCA]CTTTTTTTTTCCATC | 10138 |
rs543207770 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | YAF2 | GRCh38.p7 | 12:42223883 | CCTGTCGGGGGGTGG[A/G]GGGCAAGGGGAAGGA | 10138 |
rs543234850 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42207699 | CGATCAAGACCATCC[C/T]GGCTAACACGGTGAA | 10138 |
rs543236734 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232620 | GCATTTCTTTAAAAA[A/G]GACTTATGTAGATGG | 10138 |
rs543269323 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42173563 | TTTCCCTTCCTCTTA[G/T]CCAACTAAACATTTA | 10138 |
rs543368875 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | YAF2 | GRCh38.p7 | 12:42178532 | CCTCTCTAAAACACT[A/C]CAGCCTATGTAGACT | 10138 |
rs543406998 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42171062 | CAGTGGCGTGATCTC[A/G]GCTAACTGCAACCTC | 10138 |
rs543447843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42221443 | GGGTGTGATGGAGCA[C/T]GCCTGTAGTCCTAGC | 10138 |
rs543558394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42172975 | GAAGTAGACCTGTGG[C/T]TGCTCAGGGTTAGGA | 10138 |
rs543591586 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | YAF2 | GRCh38.p7 | 12:42207748 | ATACAAAAATTAGCC[A/G]GGCGTCGTGGCGGGC | 10138 |
rs543599067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42173553 | CACTCTCAACTTTCC[C/T]TTCCTCTTAGCCAAC | 10138 |
rs543647738 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42178811 | AGGGTGCATAATTCT[A/T]ATCTTTTATTAAGAA | 10138 |
rs543654213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42200917 | CCCTCTATATTTCAG[C/T]ATTCCCATACGCAAA | 10138 |
rs543693494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42166062 | TAGCTGGGATTACAA[A/G]CGTGTGCCACCATGC | 10138 |
rs543715342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42193539 | GACAGGATCTCACTC[C/T]GTCACTCAGGCTAGA | 10138 |
rs543837217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42229644 | CGTTAGGTGATTTCA[C/T]TGTCAGAACATCATA | 10138 |
rs544019311 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42161097 | ATCATAATTTTGCAG[A/G]CAGCTTATTAATTTT | 10138 |
rs544071665 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42206472 | AAATTAAGTGGACGC[A/G]GTGGTGCACACCTGT | 10138 |
rs544082165 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42185133 | CAGTGGGCCAAGATC[A/G]CGCCACTGCACTCCA | 10138 |
rs544164824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42163105 | GCCTTGAAGTAGAGC[C/T]CAAGAAACTGTATTT | 10138 |
rs544182580 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42204221 | GAAAATAAAATGATG[C/G]AGCCACTTTGGAAAA | 10138 |
rs544222929 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234857 | GCCACACATGGTGGT[A/G]TGCATCTGTAGTTTC | 10138 |
rs544263579 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42163833 | ATCTTTTTACAACAT[A/C]GTAAGTCACTCAACT | 10138 |
rs544270382 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42206138 | CTTCAAATCAGTAAC[G/T]TCTCTCTTTAGCTGT | 10138 |
rs544310117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42190097 | TCTGTAATCCCAGCA[C/T]TTTGAGAGGCTAAGG | 10138 |
rs544334090 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42235456 | ACACTGTTCTATACA[A/C]ACACAGATTCTACCC | 10138 |
rs544343773 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42199962 | GACAACCAATGGAAT[A/C]AATGGAAGACATCTC | 10138 |
rs544348592 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42217977 | GTGGCCTAAAAAAGA[A/C]CATGACCATGCTCAG | 10138 |
rs544390651 | in-del | -/AAACA | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42192508 | GTGAGACCCTGTCTC[-/AAACA]AAACAAAACAAAACA | 10138 |
rs544402482 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42193058 | GTGGCTCACACCTGT[A/G]ATCCCAGCACTTTGG | 10138 |
rs544440420 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42237256 | TGGGTTTTCCTTGAT[C/T]CCCACACACTAACAC | 10138 |
rs544550801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42228000 | CCCCGCCTGGCCAGC[C/T]GCCCCGTCCAGGAGG | 10138 |
rs544563499 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42181799 | TATGAACTGGGTAAA[C/T]GAATTTATAACTGTG | 10138 |
rs544611147 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42162200 | GTTCTTTAAAGCTTT[G/T]CATTTATTCATTTAA | 10138 |
rs544685185 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42190821 | TGTTTTGGGATTTGG[A/C]AAGGTTTGGTTTCTG | 10138 |
rs544688794 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42225364 | GAAGCTCTTTAGTTC[A/C]ATTAGATCTCATTTG | 10138 |
rs544699374 | snp | A/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233440 | CACCAGTCTTAAATT[A/T]ATCATCACACATTGA | 10138 |
rs544728204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42226245 | TTATATCATATAAAT[C/T]TCAACTATCTGAAAA | 10138 |
rs544738549 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42183112 | GTCATTGTTTTGAGG[A/C]GCCAAGGCCCACACC | 10138 |
rs544738633 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42176243 | AATCCACCTGGATGT[C/T]TATGAGTAGCTGGGA | 10138 |
rs544747619 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42159201 | ATCACAACTGTTAGG[G/T]TCTACAGTTTTATTT | 10138 |
rs544772581 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42176724 | CTCAGCACTTTGGGA[A/G]GCTGAGGTGGGTGGA | 10138 |
rs544773801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42175106 | TCATTTGTAATGGCC[C/T]AAAACTGAAAATAAC | 10138 |
rs544807963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42167734 | TTTCTGGCCAGGCTC[A/G]GTGGCTCACATCTAT | 10138 |
rs544857819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42204486 | GGTTATATTAGATAT[C/T]AAAAGTAATCTAGAG | 10138 |
rs544861224 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42198214 | CTTAGGGAGATGATG[A/G]TAATTATAATCCTAC | 10138 |
rs544890563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42212614 | TCTGTAAAATCATTC[C/T]ACACAATCAAATTCA | 10138 |
rs544920323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42170070 | GAGATGAGGGTCTCA[C/T]AACGTGGCCCAGGCT | 10138 |
rs544950108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42231826 | CTAATTTTCACTTGA[A/G]TGATTATCACTGGCA | 10138 |
rs544999684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42217340 | ACTCTGATAATACAG[C/T]TTTGCAACTAGCAAA | 10138 |
rs545020340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233207 | AAATCTTTTTTATAG[C/T]TCTCTAAAATAACAC | 10138 |
rs545042437 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42236715 | GTTTCTAATGGACTT[C/T]GTAATATCAAAATAC | 10138 |
rs545082065 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | YAF2 | GRCh38.p7 | 12:42167156 | GAGTGGGGGGAAAGG[G/T]GAGGGAGAGTATTAG | 10138 |
rs545097011 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42179425 | TAGTGAGCCAAGATT[A/G]CACCACTGCAGTGCA | 10138 |
rs545145734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42207664 | TTGGGAGGCCGAGGC[A/G]GGCAGATCACAAGGT | 10138 |
rs545188169 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42203030 | TATCTTGGTTATTCT[G/T]GAACCTTTAATTTTG | 10138 |
rs545193866 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160473 | CTATTTTATGTAAAA[C/T]TCAAATTATGGATTG | 10138 |
rs545228020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42187058 | TAGAACCTAATAATA[C/T]AATATTGGTTTCACA | 10138 |
rs545253705 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42211814 | AGCACTTTGGGAGGC[C/T]GAGGTGGGCGGATTA | 10138 |
rs545265008 | in-del | -/C | 0.00398722 | 0.0444715 | intron-variant | YAF2 | GRCh38.p7 | 12:42196033 | TGGAGACCAGCCTGG[-/C]CAACATGGTGAAACC | 10138 |
rs545301140 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42228168 | GGTCGGCCCCCCGCC[C/T]GGCCAGCCGCCCCGT | 10138 |
rs545301962 | in-del | -/A | 0.359575 | 0.224707 | intron-variant | YAF2 | GRCh38.p7 | 12:42205055 | AATAAAGTTGTTATT[-/A]AAAAAAAAAAAAACC | 10138 |
rs545379791 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42189046 | TGTCAGGAAAGCCTT[C/T]CTGTAGAGATGATTT | 10138 |
rs545398310 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42216353 | TGGAACTTGAGAGAA[A/C]AATTAAGATTCTGTC | 10138 |
rs545436995 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42202245 | TTGTCTTTTCCTGTA[C/G]TAATACTATACTTCA | 10138 |
rs545503458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42195097 | CAAGAAACATACACA[A/G]GCAATTAAAGTACAT | 10138 |
rs545571775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42194005 | TTTGAATGGAGAAAG[C/T]ACACAGAATAAGGAT | 10138 |
rs545581469 | snp | C/G | | | intron-variant, utr-variant-5-prime | YAF2 | GRCh38.p7 | 12:42237529 | TCATGGGAGGGGGCG[C/G]CAGCCGCAAGGGCGT | 10138 |
rs545590261 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42218759 | TAACATATGTTTCAT[C/T]TGTAAATTATAATGC | 10138 |
rs545613685 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42159769 | TTGTAAAATATGGCA[A/C]GTTTCTTTTCTCTTG | 10138 |
rs545615353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42201562 | GTCGCATATCTTTTA[A/G]TTTGGTTTATAATGT | 10138 |
rs545616629 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42229932 | ATAGAATCAATATGA[C/T]ACCAAGGGGTGGAGG | 10138 |
rs545743532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42223817 | ACTCATAAGTGGGAG[C/T]TGAACAATGAGAACA | 10138 |
rs545752711 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232479 | CATATACAATTAACC[A/C]GTGTGAGTCCTCTTA | 10138 |
rs545809061 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42225276 | GCCCTTTGTCAGATG[A/G]ACAGATGGCAAAAAT | 10138 |
rs545812581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42193432 | TTTATTGCTATTTCA[A/G]AGTGTATTCCTTGTA | 10138 |
rs545837557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42177454 | TGTGTCCTCACAAGG[C/T]CTTTCCTCAGTGCAT | 10138 |
rs545867933 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | YAF2 | GRCh38.p7 | 12:42227652 | GCCCAGCAGCTGCCC[C/T]GTCTGAGAAGTGAGG | 10138 |
rs545905478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42185748 | TTGGATATAATGCTA[C/T]TATTACACATTTAAC | 10138 |
rs545963723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42214428 | AGGCTCATGCTACCA[C/T]GCCCGGCTAATTTTT | 10138 |
rs545975463 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42173748 | ATTAAGCATTTACTA[C/T]GTTCCATTAAATATT | 10138 |
rs545980949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42179339 | GCAGAGCTTGGTGGC[A/G]TGAGCCAGTAATCTC | 10138 |
rs546031860 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42214232 | ACTCCTAACCAAAGG[G/T]CTTTCAACTTGCCGT | 10138 |
rs546043272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42207703 | CAAGACCATCCTGGC[C/T]AACACGGTGAAACCC | 10138 |
rs546084906 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42215767 | TCTCTACTAAAAACA[A/C]CAAAAAACATTAGCC | 10138 |
rs546114550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42165541 | TGATCTCAGGTCACT[A/G]CAAGCTCTGCCTCCT | 10138 |
rs546129053 | in-del | -/T | | | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42156610 | CCCCTTCTTCTTCAC[-/T]TTTTTTTTCCATCCC | 10138 |
rs546133838 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42192616 | TATATTTTAATTTTT[A/G]AAACACATATGGAAT | 10138 |
rs546244442 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42221269 | AAATGCTACCACAGC[A/T]AGGTTATAAAATGGG | 10138 |
rs546312302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42171020 | TGTTTTTAGACAGAG[C/T]GAAACTCTGTCTCCC | 10138 |
rs546340357 | in-del | -/TT | 0.0023933 | 0.0345097 | intron-variant | YAF2 | GRCh38.p7 | 12:42184305 | TTCAACTTTAAAGAC[-/TT]ATTATTATTATTACT | 10138 |
rs546392684 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42164266 | AAATAGAAGGTATAA[C/G]TTTTGCAGTCTGTTG | 10138 |
rs546431427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42164899 | ACATAGTGAAAACCC[A/G]TCTCTACAAAAAAAA | 10138 |
rs546437082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42182921 | TGCATTACTTTATTA[C/T]TTTTTACAAATTGAA | 10138 |
rs546438572 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42235122 | TTTGGCAATGAGGCA[C/G]AATCAGTTCAAAGGT | 10138 |
rs546474209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42183269 | CCAATCAATAACTCA[A/G]CAATGGTGTCTAATA | 10138 |
rs546505646 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42184998 | TCTGGCCAATATGGC[A/G]CAACCCTGTCTCTAC | 10138 |
rs546566445 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42156830 | ATTCTTTGTTCCAGA[A/C]AACTGAAGGTGCCTG | 10138 |
rs546597941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42169221 | TTTGACTTCTGTGTA[C/T]CATGACATTATTTAA | 10138 |
rs546689929 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232734 | ATGACAAGAAAACAA[A/C]GATGCTGAAAAGATT | 10138 |
rs546707196 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42225989 | GCCATTTTCACAATA[C/T]TGATTCTTCCTATCC | 10138 |
rs546723137 | in-del | -/CTTC | 0.00716266 | 0.059414 | intron-variant | YAF2 | GRCh38.p7 | 12:42197259 | TTCTAGACTGGTGTT[-/CTTC]CTTTGGCTATGAACC | 10138 |
rs546724932 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233936 | AGCACTTTGGGAAGC[C/T]GACGCAGACGGATCA | 10138 |
rs546753366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42167386 | AATAACTAAGATCCC[A/G]TTATATATGACAGAA | 10138 |
rs546802000 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42174667 | GATTTTTTTATGCAT[C/G]CTAAAAGCACTCCTC | 10138 |
rs546888377 | snp | A/T | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42159928 | GTCCGCTAGTAAACA[A/T]TACAATAAATGAATG | 10138 |
rs546956640 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42219138 | ATAATGGCATAAATG[A/T]CCTGGATGAAGTGAA | 10138 |
rs546963362 | snp | C/T | | | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42161501 | CCTGATACCTTATAA[C/T]AAAGGAGACCAAATA | 10138 |
rs546978263 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42215337 | GCACTTTGGGAGGCT[A/G]AGGTGGATCGCAAGA | 10138 |
rs547044627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42188063 | CCAGAGCCAGAACCA[C/T]CCAGCTAAGCTGCTC | 10138 |
rs547181068 | in-del | -/AT | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42167245 | AAACCACCATGACAC[-/AT]GTCTATCTATGTAAC | 10138 |
rs547205792 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42217655 | ACTTATATTTAATTA[A/C]CACCAAAAAAATCAC | 10138 |
rs547216156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42218084 | TCTTAAGTCTATATA[C/T]ACTGCTTACTCCTAT | 10138 |
rs547228046 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42158635 | GGTGTCAGTTAGCAC[A/G]CTTAATCTCCATGCT | 10138 |
rs547239322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42203574 | ATTTCTGTTCATAGT[A/G]TAAGAGTGGTTTTTT | 10138 |
rs547250493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42209381 | TCAGCCTGGGCAACA[C/T]GGCAAAACCCCATCT | 10138 |
rs547376619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42165250 | GAGGAGGAGTTATTA[C/T]AGACAGAGAGGAAAT | 10138 |
rs547438680 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42208581 | CCAAACACTAGCCAA[A/T]AAGGGTATTAACTGG | 10138 |
rs547440146 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42193101 | GGGCAGATCACTAGA[A/G]GCCAGGAGTTTGAGA | 10138 |
rs547440248 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42201018 | TAAAACAATACAGAA[C/G]CTAGACACAGAAAGT | 10138 |
rs547512640 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42165808 | TTTTAATGTAACTAA[A/C]TCCTCATCAACTGTC | 10138 |
rs547564142 | snp | A/C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42171761 | GAGTTCAAGACCAGG[A/C/G]TGGGCAACATGGTGA | 10138 |
rs547614485 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42237800 | CCGGGCCCCGCGGCC[C/G]CCCCCGCCCCGCCCC | 10138 |
rs547653238 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42187611 | TTCAAATCCTACTCT[A/G]ATACTTACGTAAAAA | 10138 |
rs547654355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42194791 | GGAAATATCCCCTCA[C/T]GAAATATACATTCTG | 10138 |
rs547709674 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42222984 | CTGGTGTTGGAAACT[A/C]AGTAAAAAGCTGTGT | 10138 |
rs547827171 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42236016 | CAAATAAACATATAG[C/G]CTCTTCTAGTTTCAG | 10138 |
rs547899562 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42211906 | ATACAAAAATTAGCC[A/G]GGTGTAGTGGCAGGT | 10138 |
rs547908325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42179268 | TGAGGTCAGGAGTTC[A/G]AGATCAGCCTGGCCA | 10138 |
rs547962807 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42177002 | TCCCTCAATTGTTCT[G/T]CTACAGGCCATTCTT | 10138 |
rs547976760 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42209489 | GGATGGCTTGTGCCC[A/G]GGAGGCAGAAGTTGC | 10138 |
rs547996654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42185938 | GGCACAGTGGCTCAC[A/G]CCTGTAATCCCAACA | 10138 |
rs548055815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42179071 | CAAAAAGAAAGAAAA[A/G]ATACACTTGTCTGGG | 10138 |
rs548084110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42214002 | CTTTCTATTTACACA[C/T]TCCTGCAGCCTGCCA | 10138 |
rs548093452 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42164702 | CTGGACTAAATCCAT[A/T]CATATTGTGAATCTG | 10138 |
rs548149538 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42206679 | TCTTTGAAAAGTTCT[C/G]CATTATAAATCACTT | 10138 |
rs548168102 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42226315 | TATTATACAACTTGC[C/G]AAAGCTGTTCCTTAA | 10138 |
rs548170091 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42218340 | ATGCAAGTATACATT[A/T]CCCTTTTTGACTGAT | 10138 |
rs548231037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42184466 | AGGCATGTGCCACCA[C/T]GCCTGGCTAATTTTT | 10138 |
rs548268999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42177582 | GCCTCCTACCAGCCT[C/T]ATCTCCAAATACAGT | 10138 |
rs548334235 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42227716 | AGTGAGGAGCGTCTC[C/T]GCCCGGCAGCCACCC | 10138 |
rs548388905 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42227544 | AGACCCCGTCTGGGA[A/G]GTGAGGAGCGTCTCT | 10138 |
rs548397535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42220703 | TCCCTAGTATGTTCT[A/G]TAAAAGTAAAGTATG | 10138 |
rs548406698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42161441 | TTGTATTTCTGGCTT[C/T]TGTGTTTAATTTCCT | 10138 |
rs548411586 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42221529 | GCACCACTGCACTCC[A/G]GCCTGGGTGACAGAG | 10138 |
rs548540208 | in-del | -/TATC | | | intron-variant | YAF2 | GRCh38.p7 | 12:42165885 | TTTAAATTCTATCTA[-/TATC]TATCTATCTATCTAT | 10138 |
rs548568577 | in-del | -/ACACACACACAC | 0.00755907 | 0.0610114 | intron-variant | YAF2 | GRCh38.p7 | 12:42223327 | CAGTTTCTTTAAAAT[-/ACACACACACAC]ACATACACACACACA | 10138 |
rs548640892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42204065 | CAGCAAGACCCCATC[C/T]CTAAAAAAACCAACC | 10138 |
rs548642652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42196067 | TCTCTACTAAAGACA[C/T]AAAAATTAGCAGGGT | 10138 |
rs548658050 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42159841 | ATATGATACAGAAAA[C/T]ACCAGTGTTCAATGA | 10138 |
rs548754593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42196689 | TGCAAACTGTTGCAA[C/T]GAACAAAGTGTTGCT | 10138 |
rs548803637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42205625 | TGATCCACCCGCCTC[A/G]GCCTCCCAAAGTGCT | 10138 |
rs548837960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42197705 | GAAAACATGTAACCC[A/G]AAAAACCTCACAATC | 10138 |
rs548850480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42198320 | AGGCACAGTGGCTCA[C/T]GCCTATAATCCCAGC | 10138 |
rs548953778 | snp | A/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42235255 | ACTTGCCAACCTTAC[A/T]CTGGAAATTACCCTG | 10138 |
rs548969868 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42182262 | TGAAATTCTGTTAAC[A/T]TATGATGTGGCCGGG | 10138 |
rs549030255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42179948 | CTAAAATAAGTCTTT[C/T]CTAGGTATTAATTTT | 10138 |
rs549149443 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42188449 | GGAGTGCAGTGGTAC[A/G]ATCTTGGCTCACTGC | 10138 |
rs549299249 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42175404 | AAAAATGGGCACAAA[C/G]AAACTCCAGAAAATA | 10138 |
rs549343879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42194628 | TAAATAAATAAATAA[A/G]TCTAAGCCATTCTTA | 10138 |
rs549375357 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | YAF2 | GRCh38.p7 | 12:42198541 | CAGTGAGCTGAGATC[A/G]TACCACTGCACTCCA | 10138 |
rs549378034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42217565 | CAAGACACTGTGATG[A/G]GCATTGAGAATTTTA | 10138 |
rs549463882 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42213949 | AGGGCATTAATACGC[C/T]CCATTATCTTTCACC | 10138 |
rs549469757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42221726 | ACCTCACCCAGCAGA[C/T]TGCTAAATATTATGT | 10138 |
rs549529298 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42231726 | ATCAGAAATTATATT[A/C]ATTGATACCACCACT | 10138 |
rs549558387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42216784 | CCCCAAATTCAACAA[A/G]TCTATAGGCAAACTA | 10138 |
rs549565442 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42218687 | GGATTATGACTGGCT[C/T]CCAAAATAATCTTAT | 10138 |
rs549583241 | in-del | -/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42169960 | ACTACAGCCTCAACC[-/T]TCTGGGTTCAAGCTA | 10138 |
rs549628141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42166329 | TTTCTTGAAGAGACA[A/G]ACATTCTCTCTGCTT | 10138 |
rs549768826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42222860 | TCACAGTGGCTGACA[C/T]ACAGTAAGTGCTCTG | 10138 |
rs549799298 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157897 | AGTGCTGGGATTACT[A/G]GCATGAGCCATCACA | 10138 |
rs549800429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42205941 | TTCTTGAAAATTCTT[A/G]ATCATTTTTCCTTTA | 10138 |
rs549837558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42207527 | TTTTAAAGGGAAAAA[C/T]TGTTTTTAAGAAAAA | 10138 |
rs549867070 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42165178 | CAAACATAGGCCCTG[C/G]CCTCATGCGCTAAAA | 10138 |
rs549881446 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42215295 | TCCAGTGTAGGCTGG[G/T]TGCAATGGCTAACAC | 10138 |
rs549903831 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157194 | TGAGGGCCTCATGCT[A/G]CTTCAACTCATGGTG | 10138 |
rs549941486 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42185785 | CAGAATGGTGTAAAC[A/G]TAACTTTTATATGAA | 10138 |
rs549948028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42200391 | AGGCTGAAAACTATT[C/T]ACCTTCTTATCCCTA | 10138 |
rs550071681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42201934 | TCATTTACCCTTGAT[A/G]TCTTTAACCTTGATG | 10138 |
rs550091971 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42192354 | CTCCACACACACACA[A/C]AAAAATTAGTTGGGC | 10138 |
rs550103242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42163656 | ACTTAAAGATTATGA[C/T]TTTGTACCTCAATTC | 10138 |
rs550104817 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238542 | GTTCCCCCGTTGCCC[C/G]CTTGGTACCCCCGGC | 10138 |
rs550227534 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42182988 | CGCCATTTTTCCAAC[A/T]GCATGTAAAAGTTGT | 10138 |
rs550266174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42183377 | GGCATGTCAAAAGCC[A/G]AGACAGACCAAAAGC | 10138 |
rs550351200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42190378 | AATGAAAAAGAATTG[C/T]TAATACTGTTTATAT | 10138 |
rs550396765 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42193083 | CTTTGGGTGGCCGAG[G/T]GGGGGCAGATCACTA | 10138 |
rs550402962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42176881 | CTAAGGCAGGAGAAT[C/T]GCTTGAACCCAGGAG | 10138 |
rs550408875 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42185321 | CACAAAGTGGTTTCT[G/T]GATATGGAATCTACT | 10138 |
rs550431530 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42165225 | CTGTGTGTTGTGATA[A/G]AGAAAACAGGAGGAG | 10138 |
rs550466257 | in-del | -/TACAC | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42175260 | ATTGGACCAAAAAAA[-/TACAC]TACACACTGTATGAT | 10138 |
rs550504872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42172599 | CCAGAGATAGCAGAA[A/G]TGCTATTCTGAAGTC | 10138 |
rs550520922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42219724 | CACCTCATTATCTTA[C/T]CCAGAAAAAATACAG | 10138 |
rs550597372 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42198139 | AAGTCATCATGTAAG[C/G]AATCTTTCTGGTTCA | 10138 |
rs550609491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42191223 | TTTATATCGTTTTCA[C/T]TCTAAACACTTTTGT | 10138 |
rs550662604 | in-del | -/ACA | 0.00914312 | 0.0669923 | intron-variant | YAF2 | GRCh38.p7 | 12:42206953 | AAATTGTTAACATTT[-/ACA]ACGTTTGCTTTACCT | 10138 |
rs550669478 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42196577 | TGAATTATCTACAGA[A/G]ACTAAATAAGTAATA | 10138 |
rs550677119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42235183 | TGTGCGTCACACAAA[C/T]AAATCATTAGCAAAC | 10138 |
rs550740567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42211683 | TCGGGAGGTGGAGGT[C/T]GCAATGAGCCAAGTC | 10138 |
rs550757456 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42194236 | GTGTTTATAAAATCT[A/G]CAGTGGCATACAGTA | 10138 |
rs550772870 | in-del | -/AGG | 0.00835141 | 0.0640778 | intron-variant | YAF2 | GRCh38.p7 | 12:42198178 | ACTTTAAAGCAAAAA[-/AGG]AGAAGTTAGTGGCCT | 10138 |
rs550794200 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42226305 | ATCATAACAATATTA[C/T]ACAACTTGCCAAAGC | 10138 |
rs550812220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42168039 | TTTAAGTAATATTTA[C/T]GAATAATATACAAAT | 10138 |
rs550815761 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | YAF2 | GRCh38.p7 | 12:42227681 | GGAGCCTCTCCGCCC[A/G]GCAGCCACCCCATCT | 10138 |
rs550828090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42218309 | CTAGGTGCACACAAT[C/T]ACCAACCACAATGAT | 10138 |
rs550862273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42190344 | GTGAGTGCAACCGTC[C/T]CAAAAAAATAAACAA | 10138 |
rs550868565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42170419 | TCTTGCGTATCTTAA[C/T]GATAACAAAGAATAC | 10138 |
rs550909410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42225131 | CTAATGACCAGTGAT[A/G]AGTTTTTCACATTTG | 10138 |
rs550969746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42209452 | AACTGTAGTCCCAGC[C/T]ACTCAGGAGGCTGAA | 10138 |
rs550995658 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42174813 | AAGTTAAATTTTGCT[A/G]AATTTTATAAATAGA | 10138 |
rs551033215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42210105 | GCCCGGCCAACTAAA[C/T]GTATAATTTTTTAGA | 10138 |
rs551038673 | in-del | -/A | 0.399611 | 0.200291 | intron-variant | YAF2 | GRCh38.p7 | 12:42179790 | CCCTGTCTAAAAGGC[-/A]AAAAAAAAAAAAAAA | 10138 |
rs551074735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42175332 | GTGACAGAAAGCAGA[C/T]CAGTAGTTGCCTAGC | 10138 |
rs551088073 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42216745 | CTGCTTCAGAGATCT[A/T]CCCTCTCAAATTTTC | 10138 |
rs551112117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42168718 | CACTGTTCTCAAAGT[A/G]GTTACAGTAAGCAGA | 10138 |
rs551145489 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42203376 | TCTTTTAATATTTCT[A/G]GGGAGCATCTCATCT | 10138 |
rs551154659 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42218748 | CATTATGAATTTAAC[A/G]TATGTTTCATCTGTA | 10138 |
rs551203730 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42211928 | GTGGCAGGTGCCTAT[A/T]ATCCCAGCTACTCAG | 10138 |
rs551253750 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42161394 | ATGTCTTCCAATCTC[A/G]TAAAAAGAAAAAAGC | 10138 |
rs551265383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42204776 | CATATGCTACAATGC[A/G]GATAAACCTTAAACA | 10138 |
rs551309511 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232817 | TTACTTTTAAAAGAA[G/T]CTGAAATAACTCACT | 10138 |
rs551386929 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42226612 | GAGGCTGCAGTAAGC[A/T]ATATCCACACCACTG | 10138 |
rs551461102 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42169613 | GAGACAGGTTTCACC[A/G]TGTTGCCCAGGCTGG | 10138 |
rs551527175 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | YAF2 | GRCh38.p7 | 12:42201819 | TCAAGTGAACCATCT[G/T]CCTTGGTCTCCCCAG | 10138 |
rs551537991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42195412 | AATACTAAAACAAGA[C/T]TTCTAAAAAGTATTA | 10138 |
rs551539628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42194473 | ACACGGTGAAAACCC[A/G]TCTCTACTAAAAAAA | 10138 |
rs551547084 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42173044 | TGAGAGAGGGAGAGA[C/G]AGACAGAGAGAGAGA | 10138 |
rs551591815 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42236314 | TAGTAACCACAATCA[C/T]TTTAGCAAATACTTT | 10138 |
rs551670756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42223007 | AGCTGTGTCTTTCAT[C/T]ATCTGTCACTTGTGC | 10138 |
rs551673917 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42189139 | AGGTAGAGAGAGCAC[G/T]ATGAGCAAAGTCACC | 10138 |
rs551717010 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime | YAF2 | GRCh38.p7 | 12:42237532 | TGGGAGGGGGCGGCA[G/T]CCGCAAGGGCGTCCT | 10138 |
rs551735730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42201097 | TAAATATAGATGTAG[A/G]TAATTCTCCATTGTA | 10138 |
rs551797187 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | YAF2 | GRCh38.p7 | 12:42193712 | TTTTGCCCTGTTGCC[C/T]AGGCTGGTTTCCAAC | 10138 |
rs551805966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42173882 | AAAGAGAAGCTATTC[A/G]ATTAGAATGTCCACA | 10138 |
rs551821743 | snp | A/G | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239568 | AGCTAAACTACATAG[A/G]AAATAATACAGTCAG | 10138 |
rs551846878 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42227756 | GGGAGGTGGGGGGGT[C/T]AGCCCCCCGCCTGGC | 10138 |
rs551888795 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238746 | GAACGACTTTCCTGG[A/C]CTCCGCTGTCCTTAG | 10138 |
rs551895769 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42192171 | ATAAAACTTGAGAGA[C/T]AGGCAGACCAGGCCA | 10138 |
rs551912044 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42230759 | ATGCCACATACAAAG[G/T]AAAGAATATACAGAT | 10138 |
rs551951917 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239368 | TTTCCCTACCTCTGC[C/T]TCCCTCTCCCATAAG | 10138 |
rs552044519 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | YAF2 | GRCh38.p7 | 12:42171980 | AACAAAAAAAGAGTT[A/T]AAAAACAAGTATTTA | 10138 |
rs552065694 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42230428 | ATTATGGCCTTGAAC[A/G]CTATCCTAAGGATCT | 10138 |
rs552071628 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42165821 | AACTCCTCATCAACT[G/T]TCATGCCTAATCCTA | 10138 |
rs552143175 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42219702 | GATGAATACCTCACA[C/G]CCCGTCCACCTCATT | 10138 |
rs552149462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42212280 | AAGCTCATATGAAGA[C/T]ATTACATTACCTTTA | 10138 |
rs552157347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42212885 | TCCATTTCTAATTGG[A/G]ATAAATATCAGAAAA | 10138 |
rs552174430 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42228416 | CAGCCGCCCCGTCCG[A/G]GAGGGAGGTGGGGGG | 10138 |
rs552248295 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | YAF2 | GRCh38.p7 | 12:42185205 | AAACAAACAAACAAA[A/C]AAACAGAACTAGAAT | 10138 |
rs552337122 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42176270 | GGGACTACAGGAGTG[C/T]ACCATCACGCCAGCT | 10138 |
rs552375427 | in-del | -/GAAG | 0.00561121 | 0.052782 | intron-variant | YAF2 | GRCh38.p7 | 12:42230261 | CTCCTTCAAGAAAGA[-/GAAG]AAAGAAAGAGAAGAA | 10138 |
rs552411206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42215156 | TTTGAAATTCATAAG[C/T]CACTCACTGATTTTT | 10138 |
rs552435054 | in-del | -/TTTT | 0.357238 | 0.225832 | intron-variant | YAF2 | GRCh38.p7 | 12:42165774 | CTGCGCCCGGCCAGG[-/TTTT]TTTTTTTTTTTTTTT | 10138 |
rs552505860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42169614 | AGACAGGTTTCACCA[C/T]GTTGCCCAGGCTGGT | 10138 |
rs552531971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42187715 | TGTCTTACAAATAAG[C/T]ATTAATAAATAATAA | 10138 |
rs552577890 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42223690 | AATAATGGCCACATG[C/G]AGCCATAAAAAAGGA | 10138 |
rs552704989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42162574 | GAGGGAAGGAGGGAA[A/G]AAGTAAGATAAAAAT | 10138 |
rs552710347 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42217909 | GACCATGAAATTGTG[G/T]AGGATGGGGAAGTAG | 10138 |
rs552716127 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42206420 | TCGAGACCAGCTTGG[C/T]CAACATGGCAAAACC | 10138 |
rs552740202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42163336 | ATCCTTAAGTGATGA[C/T]AAGTCACTGAAGAAA | 10138 |
rs552763829 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42181690 | TAACTCATAAAAGCA[C/G]AGATGAAAATAATTC | 10138 |
rs552839674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42225320 | GTAGGTTGCCTGTTC[A/G]CTCTGATGATAGTTT | 10138 |
rs552858684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42192258 | CATGCCTGTAATCCC[A/G]ACAGTTTGGGAAGCT | 10138 |
rs552883862 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42211622 | TGGTGGCATGCGCCT[C/G]TAATCCCAGCTATTA | 10138 |
rs552919990 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42192967 | ATAGTACTCATGTGT[C/T]TGCAGTGATGCTGAT | 10138 |
rs553113020 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42158977 | TAGCTGGTATTCCAT[G/T]GAAAGTATCTTATAA | 10138 |
rs553125723 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42158364 | TTAGGTCATCCAAGA[A/G]GGCAGGAAAATAACT | 10138 |
rs553138013 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42173366 | TTCCTTGACAAATAC[G/T]AAGATAGTCCTTGGT | 10138 |
rs553179760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42175590 | CTAATCAAATTAAAA[C/T]GGGAGGCCAGGCACG | 10138 |
rs553194532 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42219945 | TGATCTATATTATAA[C/T]TGAAAAACAAAGTTC | 10138 |
rs553207651 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42191892 | CAGGAGTGTTCAAGA[C/T]CAGCCTGGTCAACAT | 10138 |
rs553219414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42195618 | AGCTTAGAGAAATGA[A/G]TCATCCACTCAATAA | 10138 |
rs553224585 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42177504 | AACCTCTCCCTCTTC[C/T]TACAAGGCCACCAAT | 10138 |
rs553263279 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | YAF2 | GRCh38.p7 | 12:42202412 | GGCTCCCTCACGATC[C/T]TTACCAATCAGTACC | 10138 |
rs553295354 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42202903 | CCGCCTCTCAAAGTG[A/C]TGAGATTACAGGCAT | 10138 |
rs553322623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42160945 | TATTTAAGGCAATTT[A/G]TGTGTAACTAGCCAC | 10138 |
rs553371415 | in-del | -/ATTATC | | | intron-variant | YAF2 | GRCh38.p7 | 12:42217595 | AAAAATATTATTACA[-/ATTATC]ATTATCATTAACTAA | 10138 |
rs553392976 | in-del | -/GTG | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42218460 | ATTTTATTGTGTAAA[-/GTG]GCCTATGAATTGTTG | 10138 |
rs553460204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42208889 | AATTGGATAGCAGGA[A/G]GCCTCAAGTATCCAG | 10138 |
rs553534943 | snp | A/C/T | 0.00199529 | 0.0315338 | intron-variant | YAF2 | GRCh38.p7 | 12:42178215 | GATCTGTGATCCTAT[A/C/T]GCACTTGTTTTCAAC | 10138 |
rs553638293 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42202303 | CTTACATAAAGCATA[A/C]AAATACTGAATGTAC | 10138 |
rs553659867 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | YAF2 | GRCh38.p7 | 12:42236474 | TACAAAAAACAAGCA[C/T]GTCAAAACCAGCGAG | 10138 |
rs553686389 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42156811 | TTTCTTCAGTTTTTC[C/T]TACATTCTTTGTTCC | 10138 |
rs553735486 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42200787 | CTCAATATTCATACA[C/T]ATCAAAAGGTAGCAT | 10138 |
rs553769225 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239774 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCGGATCA | 10138 |
rs553844642 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42236241 | ACTCCAACCTTACAC[A/T]GCCAAGAAGATACTC | 10138 |
rs553845869 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42206523 | CTGAGGCTGGAGAAT[C/T]GCTTGAACCCAGGGG | 10138 |
rs553868910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42193351 | AGCACATGCAATTAC[A/G]TATAGTCCATAAAAC | 10138 |
rs553959905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42214362 | CTGCAACCTCCCCTT[C/T]TTGGGCTCAAGCCAT | 10138 |
rs553987411 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42193988 | AATAAAGTAAAAAAA[A/T]TTTTGAATGGAGAAA | 10138 |
rs554006539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42179299 | ACGTGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 10138 |
rs554014871 | snp | C/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42231998 | AAAAGACTAGCTCTG[C/T]TTGCAAGACAAACTA | 10138 |
rs554023726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42229502 | CAAAGTGAATAAGAC[A/G]GTCTCTGCCCTGTAG | 10138 |
rs554068639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42216560 | AAAAAAATAAAGATG[C/T]TCCTCAAAAGTCTCT | 10138 |
rs554118327 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42178406 | ACAAGATCAAATCAG[G/T]ATCTGCCAGGTGAAG | 10138 |
rs554161520 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | YAF2 | GRCh38.p7 | 12:42208210 | AGGCGGGCAGATCAC[C/T]TGAGGTCAGAAGTTC | 10138 |
rs554200275 | snp | A/G | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232536 | ATCTCCTAGAATAAG[A/G]AGTCTCTGAACAACT | 10138 |
rs554267751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42169934 | GGAGTGCAGTGGTAC[A/G]ATCACAACTCACTAC | 10138 |
rs554280440 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | YAF2 | GRCh38.p7 | 12:42227867 | TCAGCCCCCCGCCCC[A/G]CCAGCCGCCCCGTCC | 10138 |
rs554410863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42198698 | TGCTCTGTAAAATTC[C/T]GAAATGGAGAGCGGG | 10138 |
rs554461465 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42205330 | ATCAACTGCAAACAA[C/T]CAGCTTTGACTGATC | 10138 |
rs554461702 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42173337 | TCCTGGCAGGTGGTA[C/T]CAGGAAGACTTGATT | 10138 |
rs554491702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42164188 | ATGCCATGATTAGAC[C/T]GTATTTGTCAGATAT | 10138 |
rs554493544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42171413 | GGATCACTTGAGGCC[A/G]GGAGTTAGAGGGGCT | 10138 |
rs554618553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42219411 | TTGAAGGAATGTACA[A/G]CTGTGTACAGATACT | 10138 |
rs554706218 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160245 | CACTATGTTATAAAA[A/C]ATTTAAATTCGTTAC | 10138 |
rs554731182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42219937 | TCTCCACATGATCTA[C/T]ATTATAATTGAAAAA | 10138 |
rs554742708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42213002 | ATAAAACAGATCAAG[A/G]AGCAATAATGCAAAT | 10138 |
rs554754755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42205983 | CCACTCCTCTGTGTA[C/T]GCTCTCTTCTAAAAC | 10138 |
rs554852522 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42175967 | CATATCCACTTGGGG[C/G]TAGGCTTGGTGGCTC | 10138 |
rs554982454 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | YAF2 | GRCh38.p7 | 12:42195440 | TTACCAGAATTTAAA[A/G]AAGGAAAAGGTAAGT | 10138 |
rs555003807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42203840 | GTAACTTTCCCTCTT[C/T]TTCTGTTCTCTGAGT | 10138 |
rs555060189 | in-del | -/AAAGAAAAGAAAA | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234196 | AAAAAAAAAAAGAGA[-/AAAGAAAAGAAAA]GAAAAGAAAAGAAAA | 10138 |
rs555094212 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42224626 | AGTGAGAATACGTGG[C/T]GTTTGGTTTTCTGAT | 10138 |
rs555096385 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232990 | AAGCGGTTCTAATTT[A/G]CAAAACTGTAAAATT | 10138 |
rs555122222 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42213850 | ACTCATTCTCTTTTA[A/T]CTAATCTCAAAATTC | 10138 |
rs555161430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42225176 | GTCTTCTTTTGAGAA[A/G]TGTCTGTTCATATCC | 10138 |
rs555182407 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42180880 | TTGAATCCAAGAGAC[A/G]GAGGTTGCAGTAAGC | 10138 |
rs555254829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42183041 | TCATAAAATGTTTTC[A/G]TTATTATTATATCTG | 10138 |
rs555283413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42235287 | TCATTAATAAGTCAA[C/T]TATGGAGAATTATTT | 10138 |
rs555298322 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42183012 | AAGTTGTCTCTGTGT[C/G]GCATTTTGGTAATTC | 10138 |
rs555329675 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42178556 | GTAGACTATGACAAA[A/T]AATCATTATAAATAC | 10138 |
rs555405047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42217795 | ATATATCATCACTTT[C/T]AGCAAAGAATTCTTT | 10138 |
rs555435628 | in-del | -/CGCCTGGCCAGCCGCCCCGTCCAGGAGGGAGGTGGGGGGTCAGCCCT | | | intron-variant | YAF2 | GRCh38.p7 | 12:42227988 | GGGGGGTCAGCCCCC[lengthTooLong]CCGCCCGGCCAGCCG | 10138 |
rs555462317 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42186065 | GCATGGTGGTACATG[C/G]CTATAATCCCAGCTA | 10138 |
rs555531318 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | YAF2 | GRCh38.p7 | 12:42191665 | CCAAGCATCACACTT[-/A]AGTGTTAGGAATACA | 10138 |
rs555562728 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42181527 | TATTCTCAAAGCACA[C/G]TCTCTATACCAATAG | 10138 |
rs555604870 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42202112 | TCTAGTTTCCCCCCC[A/C]ATCTAGAAAACCAAT | 10138 |
rs555663523 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42174865 | AAGGAAAAACTAGAT[A/T]ATGACATTGAAAGTA | 10138 |
rs555684227 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42208754 | AGTACAGAAATCAGA[A/C]TGCAGAAAAGGCTAT | 10138 |
rs555701691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42167595 | TATTAAAACAATACA[C/T]ATATCCTGTAACTAA | 10138 |
rs555736519 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42176333 | ACCATGCTGGCCAGA[C/T]TGGTCTCAAACTTCT | 10138 |
rs555752756 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42230205 | GAGATTGCAGTGAGC[C/G]AAGATCGCGCTACTG | 10138 |
rs555760184 | snp | A/G | 0.00438332 | 0.0466095 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42158150 | GGAAGTGTACTTGAA[A/G]TAGGGTGAAACAAAG | 10138 |
rs555799493 | in-del | -/AA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42206316 | AAAAAAAAAAAAAAA[-/AA]GTGACGTCTGGCTGG | 10138 |
rs555804806 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42166903 | TTCTGGGAAGATGAT[A/G]AAACACTGGATTTTT | 10138 |
rs555816213 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42223142 | ATATTAGAGCCCACA[C/T]TGACACCCGAGTTGT | 10138 |
rs555868341 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42201736 | CCACCACGCCTGGCT[-/A]AATTTTTGTATTTTT | 10138 |
rs555912874 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42213268 | GACATGTGAGTTAAC[C/T]TGGAAGCAGGTGTTC | 10138 |
rs555917234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42208198 | TTTGGGAGGCCGAGG[C/T]GGGCAGATCACTTGA | 10138 |
rs555926461 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42223722 | GAGTTCATGTCCTTC[A/G]CAGGGACATGGATGA | 10138 |
rs555988921 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42236461 | GCATATGATGATTTA[C/T]AAAAAACAAGCATGT | 10138 |
rs556045451 | snp | C/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42231288 | ATTTTGTATGAAGAG[C/T]GGCATCGTATATTTT | 10138 |
rs556099457 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42207614 | CTGGTAAGTGTAGGC[C/T]GGGCACGGTGGCTCA | 10138 |
rs556115962 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42214225 | AAAACAAACTCCTAA[C/T]CAAAGGGCTTTCAAC | 10138 |
rs556148361 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | YAF2 | GRCh38.p7 | 12:42198623 | GAATGAAACATCACA[A/T]TTTATCTAAAGAAAT | 10138 |
rs556159844 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42193826 | GTTATCACAGCAGAT[G/T]ACGGCTCCATGCATG | 10138 |
rs556229141 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42201944 | TTGATGTCTTTAACC[C/T]TGATGGTTCATTCTT | 10138 |
rs556231152 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42167452 | CAAAAAATAAATGTT[C/T]TCCTTCTTTGAAGAC | 10138 |
rs556239348 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42216095 | CTAAAGTCATTGTTA[G/T]AGGCATAGACTTAAA | 10138 |
rs556257434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42199975 | ATCAATGGAAGACAT[C/T]TCAAATAGTTTAAGG | 10138 |
rs556293245 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42227494 | CTCTGCCCCGCCGCC[C/G]CATCTGGGATGTGAG | 10138 |
rs556294948 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42190849 | CTGGCTCTCCCTTTT[G/T]TTATTAACCTAAAAT | 10138 |
rs556318473 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42197969 | AAACTAGATATGGTT[A/C]TACTTTGCAATATGT | 10138 |
rs556370717 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42219897 | TGGACCACACTTTGA[C/T]AGCAACATCCTACAT | 10138 |
rs556400992 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238241 | TGTTTGTCAATAAGG[A/G]GGATAATAAGCCGGG | 10138 |
rs556496573 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42220252 | TATGAAAATAATCAT[G/T]ACTATCTTCCTCCTT | 10138 |
rs556506805 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42184577 | AGCCTCTCAAAGTGC[C/T]GGGATTACAGGCATG | 10138 |
rs556528263 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42181849 | AGAAAAGTATGAATG[A/T]GAAGCGTAGTAATAA | 10138 |
rs556566923 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42182412 | TATGTAATTACAGAC[A/G]ATCTATTTGAGAAAG | 10138 |
rs556593075 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42191556 | TTTATACTTTTAACA[A/G]GCATGTTTGGTCTTG | 10138 |
rs556675248 | in-del | -/GCAGGAGAATGGCGTGAAC | 0.316445 | 0.243321 | intron-variant | YAF2 | GRCh38.p7 | 12:42207794 | ACTTGGGAGGCTGAG[-/GCAGGAGAATGGCGTGAAC]GCAGGAGAATGGCGT | 10138 |
rs556824273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42177279 | CTTGGGCTGTCATAA[C/T]AAAATACCATAGACT | 10138 |
rs556846153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42221153 | ATTTATAAGTAGTAG[A/G]TCTAATGTTAGAAAC | 10138 |
rs556861019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42177743 | CCCTCACTTCTTCCA[A/G]GTCTCTGTTCAAACG | 10138 |
rs556897812 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42170905 | AATACAAACATATTT[A/C]TTTCCCCTAATATCC | 10138 |
rs556899754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42189543 | CATGATGATGCACAG[C/T]AGCAGAAATGTGAAA | 10138 |
rs556900393 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42226117 | AAGTTGTATTCCTAG[A/G]TATTTTATTCTCCTT | 10138 |
rs556920812 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42161083 | GCTTCTATAGCTGTA[C/T]CATAATTTTGCAGAC | 10138 |
rs556965666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234110 | TGGGAGGTGGAGGTT[A/G]CAGTGAGCCGAGGTC | 10138 |
rs557015377 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42159037 | AACACTAAAGAATGA[C/G]GTATATAAATGTTTT | 10138 |
rs557031314 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42217022 | CTCCCATCTGGCATT[A/C]CCCTTGTTCAGGACA | 10138 |
rs557053017 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42207137 | CCATATCATTCACAC[C/G]AAAGAAACTATGAGA | 10138 |
rs557116921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42166548 | TTGAATGACTACTTA[C/T]ATGAGAAATCATATA | 10138 |
rs557184036 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42162677 | ACAGTTTTTAAAAAA[A/T]CTTTTTTTCTCCTGT | 10138 |
rs557254780 | in-del | -/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42188872 | TGAAGATAGATGGTT[-/C]TTATCTCATCATGGA | 10138 |
rs557254863 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42223946 | TCTTAAAACCTAGAT[G/T]ATGGGTTGATGGATG | 10138 |
rs557324355 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42208620 | AAGGTACTGTATTAA[A/G]TAAATTCCATGAATT | 10138 |
rs557432335 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42168936 | GGGCTCATACCACCC[C/T]TCCCATCATAAGAAC | 10138 |
rs557474591 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42202096 | TTGCTTGAAGCAGAG[A/G]TCTAGTTTCCCCCCC | 10138 |
rs557521832 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42158526 | AAACCCTATAAATTA[C/G]ATGTGATTACCATTA | 10138 |
rs557526677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant, missense | YAF2 | GRCh38.p7 | 12:42210425 | CCTTCTGTTCAGCAT[A/G]AGAATCTTCCTGATG | 10138 |
rs557528337 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42203035 | TGGTTATTCTTGAAC[C/G]TTTAATTTTGCACAG | 10138 |
rs557587313 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42203693 | TTTCAAATATTGAAC[C/T]GTCCTAAACTCCTAT | 10138 |
rs557603245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42197012 | GTGTCTGTTTTGTTC[A/G]CTTCTCAGAAAGTAC | 10138 |
rs557617551 | in-del | -/TA | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42168497 | GAAAGACAGAAATTT[-/TA]TGTCATAAAATTTAA | 10138 |
rs557701687 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42164557 | GAAAGAAAAAGAGTA[A/T]TAAAAACAATGACAT | 10138 |
rs557728584 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233235 | CACCTATGAGAAACC[A/T]AAAGGACTGTTATAA | 10138 |
rs557772367 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42224370 | AATTTAGGTGAAGAA[A/T]ACAATATATTTCTTT | 10138 |
rs557774043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42185459 | TTTTGAAAGAAGTTT[C/T]GCTGTGAGTAAAATG | 10138 |
rs557835301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42179129 | AGACTGGGATAGAGC[C/T]CAGTATCCTCTTATT | 10138 |
rs557838304 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | YAF2 | GRCh38.p7 | 12:42227964 | GCCACCCTGTCCGGG[A/C]GGGAGGTGGGGGGGT | 10138 |
rs557932340 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | YAF2 | GRCh38.p7 | 12:42185201 | AACAAACAAACAAAC[-/A]AAAAAAACAGAACTA | 10138 |
rs557956194 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42163253 | AGAGCAGAGTGGCAG[A/G]GTGAAAAAAAACCAA | 10138 |
rs557967588 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42186754 | GAAGCAGATTAGTAT[G/T]AAATTTGCCAATGCC | 10138 |
rs558016670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42223818 | CTCATAAGTGGGAGT[C/T]GAACAATGAGAACAC | 10138 |
rs558044239 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42159046 | GAATGAGGTATATAA[A/G]TGTTTTAATCACAGA | 10138 |
rs558062410 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42208168 | CGCCATGGCTCATGC[A/C]TGTAATCCTAACACT | 10138 |
rs558151042 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42225329 | CTGTTCACTCTGATG[A/G]TAGTTTCTTTTGCTG | 10138 |
rs558156032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238089 | CTAGCGAGGCGGCCA[C/T]CCGAAGCCCTGCACG | 10138 |
rs558181400 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42194441 | CTGAGGTCAGGAGTT[C/T]GAGACCAGTCTGGCC | 10138 |
rs558187340 | snp | A/G | 0.000203438 | 0.0100835 | intron-variant | YAF2 | GRCh38.p7 | 12:42212506 | AAACAAAGAAAGTGT[A/G]TAGTTTTTCCTTTAA | 10138 |
rs558215057 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42229550 | ACAATTATACTACAA[C/T]ATATTTATTCTCCAG | 10138 |
rs558234383 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42169810 | ACAAGACTAAATTTT[-/A]GGAAGTAGCAGGGTT | 10138 |
rs558252421 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42163820 | ACAGTTTATGATGAT[C/G]TTTTTACAACATCGT | 10138 |
rs558353417 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | YAF2 | GRCh38.p7 | 12:42170768 | GAGGATCACCTGAGC[C/T]TTGGGAGGTTGAGAC | 10138 |
rs558450274 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42173692 | TCTCCTTTCCAATCC[A/T]AGATTACTCTTGCTT | 10138 |
rs558469306 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42198752 | AGTTAAGATAAGAGC[C/T]CACGAACAAGTGAAG | 10138 |
rs558518545 | in-del | -/CAAA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42185201 | AAACAAACAAACAAA[-/CAAA]AAAACAGAACTAGAA | 10138 |
rs558543439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42200671 | TATCTCCCTCACCTT[A/G]CAATGACATCCAGAG | 10138 |
rs558605728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42213230 | TCTCTGGCCAACAGC[C/T]AGATGCCTGAGGCCT | 10138 |
rs558722110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42214049 | GAAGCCACAGAGCAC[C/T]TCCACACTTAAACTC | 10138 |
rs558722911 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42199897 | AGAGTTCTTTGGCAC[A/G]TAACAATTCAAGGTT | 10138 |
rs558747503 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42225489 | CTTGCCTAGGTTTCC[-/T]TCCAGGGATTTTATG | 10138 |
rs558777571 | in-del | -/TT | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42231760 | CTTCTCAGAAAAGTC[-/TT]TATACACAGAAACTC | 10138 |
rs558781481 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42206757 | TATTCTGCCAAATGT[A/T]ATCCCACTGTGCCTA | 10138 |
rs558810612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42236088 | AAAAGCAATAATATA[C/T]AGTACCAGAGATCAA | 10138 |
rs558856750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42235426 | ATATCTTCTCTAGTA[A/G]CAATACCCTGTTCCA | 10138 |
rs558899970 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42237101 | ACTGGAATAAAAACA[C/G]TAAATAAAACCTTGA | 10138 |
rs558919100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42204980 | AAAACTCTGTAAAAA[C/T]ACTAAAACCTACTGA | 10138 |
rs558955326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42176679 | ATCTTCATAACATCC[C/T]GGCCAGGTATGGTGG | 10138 |
rs559010511 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42216680 | AATGACTATCAAATA[G/T]GTATTTACAGCCCTT | 10138 |
rs559017267 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42187676 | GGAGTAAAATATATA[C/T]AGCATGAAAATACCT | 10138 |
rs559059237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42224225 | GAATTGGGTTTCATC[C/T]ACAATTCTGTAGTCC | 10138 |
rs559059477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42217103 | GATTCAGCAAGAAAG[C/T]AAGCATGACACAAGA | 10138 |
rs559063175 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YAF2 | GRCh38.p7 | 12:42190024 | TATTATACAATGCCA[C/T]AACAATTTACTTTTG | 10138 |
rs559070319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42217263 | ATGGGTATAATTTTT[C/T]TTATAAGAAAATGGT | 10138 |
rs559081329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42180299 | CCTTGTTGTGATCTC[C/T]CCTAACAGAGTGGCC | 10138 |
rs559106797 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42185508 | TGCTACAGATGAATC[C/T]TTCATGAAAGGAAGA | 10138 |
rs559117777 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42173708 | AGATTACTCTTGCTT[C/T]CATTAATTTATTTAA | 10138 |
rs559129594 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42211730 | GCCTGGGCAACAGAG[A/G]GAGACTCTGTCCAAA | 10138 |
rs559209325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42177208 | GATATAGGCTCTTCC[C/T]ATCTGATCTTCTATA | 10138 |
rs559226928 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42183068 | TCTGTTATGGTGATC[C/T]ATGATTGGTGATCTT | 10138 |
rs559239174 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42191509 | TAATCTAATGTAAAT[A/C]TTGCTTAATAGCTAA | 10138 |
rs559251937 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | YAF2 | GRCh38.p7 | 12:42227130 | TCAGTCTTTGCCGCC[A/G]CGCCGGCGAGCGCCG | 10138 |
rs559263898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42183595 | TAATCCACAGCAAGA[C/T]CCTAACTCCATTCCA | 10138 |
rs559302851 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | YAF2 | GRCh38.p7 | 12:42203344 | ATTATTTTATTAATA[A/C]AAACAGTACTTTCAT | 10138 |
rs559366162 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42165517 | CGCCCAGGCTGGAGT[A/G]CAGTGGCGTGATCTC | 10138 |
rs559369595 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42174262 | CTTGTCCTTCCACTC[A/C/T]AGCAAAATTATTTAT | 10138 |
rs559471088 | snp | C/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233180 | AACATCTAGCACTCT[C/T]TCTACTATGTGAAAT | 10138 |
rs559499586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42167091 | AGGAGCTAAACAATG[A/G]GAACACATGGACACA | 10138 |
rs559526894 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42195067 | GTTTCAGCCCTTACA[A/G]TTCAGCGTGAGAAAC | 10138 |
rs559533253 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42188722 | AAAAATGTTCTAAGT[A/G]TTCACATGTACAATT | 10138 |
rs559587649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42186972 | GCATAGGAGGTAGTA[A/G]AAATTGAGAGGAAAT | 10138 |
rs559624961 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42201730 | GCATGTGCCACCACG[A/C]CTGGCTAATTTTTGT | 10138 |
rs559631902 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42159398 | TTGAAATTCTAAATA[C/T]AACATAAAACTCTTT | 10138 |
rs559657446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42207789 | CCAGCTACTTGGGAG[A/G]CTGAGGCAGGAGAAT | 10138 |
rs559699966 | in-del | -/C | 0.00835141 | 0.0640778 | intron-variant | YAF2 | GRCh38.p7 | 12:42227188 | ACGGGCCCCACGGGG[-/C]CCGAGGGCAAGGAGC | 10138 |
rs559718684 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42201055 | AGTTTCTTAAGTTGA[A/C]ATAAATACTAATTAA | 10138 |
rs559742399 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42156985 | AATGACTTACTAAAT[A/G]GCTCAGTTCCTACAT | 10138 |
rs559744634 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42215742 | GCCTGGCCAACATGG[C/T]GAAACCCTGTCTCTA | 10138 |
rs559795609 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42211097 | ATGTTAGAATTCAGA[A/T]AAAATGCATCAATAC | 10138 |
rs560002827 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238369 | GGGAAACTCCTGCCT[C/G]GGCGCACGTGACCCT | 10138 |
rs560022256 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239212 | TGGTCTCCGAAGCTC[C/T]ACTTCTACCTCCCCA | 10138 |
rs560023547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42165040 | ACCCTGGGTGACAGA[A/G]TGAGACCCTGTCTTC | 10138 |
rs560086425 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42240143 | CTGCAGATGCTCTTC[G/T]ATTTAGAAAGGGGAT | 10138 |
rs560122801 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42178656 | TCTTCTGTCCAATGT[C/G]TCAGCACCACTTTCA | 10138 |
rs560148298 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42220637 | TTACCTGTTGAGCAG[A/C]TACCTCCCTGGCATA | 10138 |
rs560181383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42200166 | ACACTCTGGTAGTTT[C/T]GTAAAATAATAGAAG | 10138 |
rs560191246 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42227613 | CCTGGCAACCACCCC[A/G]TCTGAGAAGTTAGGA | 10138 |
rs560192190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | YAF2 | GRCh38.p7 | 12:42237450 | CCTGGGTTGCGATCA[A/G]TGTGACCCAGTTCCT | 10138 |
rs560194989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42192903 | GTTCCCTAAGATAAT[A/G]AAGCTGACAAATACT | 10138 |
rs560202718 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | YAF2 | GRCh38.p7 | 12:42228218 | GTCGGCCCCCCGCCC[A/G]GCCAGCCGCCCCGTC | 10138 |
rs560254146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42220372 | CACACCCAGATTCTT[C/T]ACATTAGCATTTAGA | 10138 |
rs560343462 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42167877 | GACGCAGGCACATGC[A/C]TATAGTCCCAGCTAC | 10138 |
rs560356485 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42177427 | CTGGCTTACAGACGG[C/T]CATGTTCTCACTGTG | 10138 |
rs560364554 | snp | C/G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42171630 | GGCCAGAACTGGGTA[C/G/T]ATAACTCCTGATCAT | 10138 |
rs560408561 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42218346 | GTATACATTTCCCTT[G/T]TTGACTGATGAATAT | 10138 |
rs560448376 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42205231 | GATTTCTTATAATTT[C/T]AAAAATCACCATTAT | 10138 |
rs560461921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42222503 | CAGCCATATAGGGGC[A/G]GTTTGATGAGCAAAT | 10138 |
rs560574481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42162509 | TAAGGTTCAAAATAC[A/G]GTCTCTAAGTTCTTA | 10138 |
rs560576298 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42174410 | CCTCTAGGACACCAC[A/C]CTCTTCACATTTCTC | 10138 |
rs560597418 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42168552 | GCTTGGCTTCTTCCT[C/T]AAATTCTTTTCGGAA | 10138 |
rs560616288 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42207677 | GCGGGCAGATCACAA[C/G]GTCAGGCGATCAAGA | 10138 |
rs560676608 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42211330 | TACTCGGGTGGCTGA[G/T]GCACGAGAACTGCTT | 10138 |
rs560689969 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42213465 | AGTCAATTCTTAATA[G/T]CCATCTCTAAAGTAA | 10138 |
rs560717216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42163214 | GTGAATACTGTTACT[A/G]CTATAAGATAAAGTT | 10138 |
rs560740514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42197469 | CATATCCTGCCACTG[C/T]TAATTCCACACTATA | 10138 |
rs560754844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42206351 | CAGTGGCTCACGCCT[A/G]TAATCCCAGCACCTT | 10138 |
rs560815321 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42190976 | AATATAACCTATTTT[A/T]AAAAATGTTCTGAGG | 10138 |
rs560822449 | snp | C/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234119 | GAGGTTGCAGTGAGC[C/T]GAGGTCACGCCACTG | 10138 |
rs560842470 | snp | A/C | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238967 | AATTAGAAAATGACA[A/C]AGCCAAGAGTCTAAC | 10138 |
rs561046896 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42168370 | TATTTTTAGTAGAAA[C/T]GGGGTTTCACCATGT | 10138 |
rs561069677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42204533 | GGGAGAATATGCATA[A/G]GTTATATGCAAATAC | 10138 |
rs561191690 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42187962 | GCAGCCCTATGAGCC[A/G]TCTTGGAAGAAAATG | 10138 |
rs561247569 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42235585 | AGAGGAAGGAAGAAG[C/G]TGAGAGGGTCGTGGT | 10138 |
rs561258398 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42167857 | TAAAGTTACTCAGGA[C/G]TGGTGACGCAGGCAC | 10138 |
rs561313056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42230468 | TTCAGCAGCCACTAA[C/T]AGGACTCAATTTTTT | 10138 |
rs561322047 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42181270 | TCATTTTAATGTGTG[C/G]TTATTCCTGTTACAC | 10138 |
rs561422665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42223367 | ACACATATATATACA[C/T]ACAAACAAAAAGATA | 10138 |
rs561424770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42231382 | ATTTGTTGCAATATG[C/T]TGTTTTGGTCCAAAA | 10138 |
rs561431625 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42224939 | TGGTTCTAGATCCCT[A/G]AGGAATCACCACACT | 10138 |
rs561484203 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42224054 | AAATAAATAAATAAA[A/T]AAATAATAATGGCCA | 10138 |
rs561495097 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233356 | CTATCATTTTCATTT[C/G]TAAATATTTGCTATC | 10138 |
rs561505423 | in-del | -/C | 0.00755907 | 0.0610114 | intron-variant | YAF2 | GRCh38.p7 | 12:42208179 | TGCCTGTAATCCTAA[-/C]CACTTTGGGAGGCCG | 10138 |
rs561511069 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YAF2 | GRCh38.p7 | 12:42189031 | ATCAGAGTGGAAATG[C/T]GTCAGGAAAGCCTTC | 10138 |
rs561604530 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42222168 | CAACAAATGATCAAC[A/G]AACATTTGTTAAATA | 10138 |
rs561620454 | in-del | -/GTAA | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42197494 | ACTATATTCTCAGGG[-/GTAA]GTAACAGCTAAACGC | 10138 |
rs561759707 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42207531 | AAAGGGAAAAATTGT[C/T]TTTAAGAAAAAAATA | 10138 |
rs561819948 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42158532 | TATAAATTAGATGTG[A/T]TTACCATTATTAGCC | 10138 |
rs561824861 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42224632 | AATACGTGGTGTTTG[C/G]TTTTCTGATCCTGTG | 10138 |
rs561829647 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42229683 | TTATACAAACCTAGA[A/T]GGTACAGCCTACTAC | 10138 |
rs561830816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42165674 | GACGGGGTTTCACTG[C/T]GTTAGCTAGGATGGT | 10138 |
rs561859912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42215911 | GCCTAGGCGACAGAG[C/T]GAGATTCCAGCTCAA | 10138 |
rs561873104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42207752 | AAAAATTAGCCGGGC[A/G]TCGTGGCGGGCGCCT | 10138 |
rs561878689 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42189550 | ATGCACAGTAGCAGA[A/T]ATGTGAAAGTTTGCC | 10138 |
rs562010388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42194323 | CTCCAGCCTTGCAAG[C/T]TCTATGATACAAGTT | 10138 |
rs562017244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42222319 | TGGCCCTATATCTAA[C/T]CTTGAAGGAAAGAGA | 10138 |
rs562035135 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42170795 | AGACTGCAGTGAGCC[A/G]TGATTGTGCCACTGC | 10138 |
rs562037993 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42159185 | CATGAAACCACCAAA[C/T]ATCACAACTGTTAGG | 10138 |
rs562070841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42214567 | GTGAGCCGCCATGCC[C/T]GGCCTCCTCTTATCC | 10138 |
rs562073813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42185171 | CAACAGAGCCAGACT[C/T]TGTCGCAAACAAACA | 10138 |
rs562206454 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42193079 | AGCACTTTGGGTGGC[C/G]GAGGGGGGGCAGATC | 10138 |
rs562245679 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239190 | ACTCCAGCAACAGCC[A/G]TCTAACTGGTCTCCG | 10138 |
rs562303005 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | YAF2 | GRCh38.p7 | 12:42176156 | AGGCTGAGGCAGGAG[-/A]AATCACTTGAATCCA | 10138 |
rs562370951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42185922 | AAGTCAGGCTGGGCC[A/G]GGCACAGTGGCTCAC | 10138 |
rs562455646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42198261 | AGAGGATCTGCTTTT[C/T]ATCAGAGCTGATATT | 10138 |
rs562467616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42198886 | TACAGCAACTACATG[C/T]GGGTACTGAGCACTT | 10138 |
rs562493005 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42171511 | CATCTCTTTAAATTA[A/G]AAAAAAAAGAAAGAA | 10138 |
rs562617288 | in-del | -/A | | | intron-variant | YAF2 | GRCh38.p7 | 12:42199791 | AAAGACTATTAGCTT[-/A]AAAAAAAAAAGTATT | 10138 |
rs562638348 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42227686 | CTCTCCGCCCGGCAG[C/G]CACCCCATCTGGGAA | 10138 |
rs562665545 | in-del | -/A | | | intron-variant | YAF2 | GRCh38.p7 | 12:42161145 | AGACAACAATGAAAT[-/A]GTTGCACCATGGAGG | 10138 |
rs562665836 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42203126 | TAAAATTCACAAAGT[A/G]ACTTTTCAGTAATAT | 10138 |
rs562748901 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | YAF2 | GRCh38.p7 | 12:42228007 | TGGCCAGCCGCCCCG[C/T]CCAGGAGGGAGGTGG | 10138 |
rs562874987 | in-del | -/G | 0.00358779 | 0.0422022 | intron-variant | YAF2 | GRCh38.p7 | 12:42193081 | ACTTTGGGTGGCCGA[-/G]GGGGGGGCAGATCAC | 10138 |
rs562883357 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42218824 | TGAGCCTTACTAATC[A/T]CGGTCCTTAAAAAAA | 10138 |
rs562904798 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42186278 | GCAGGAGCTTGAACC[C/T]GGGAGGCGGAGGTTA | 10138 |
rs562920682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42176256 | GTCTATGAGTAGCTG[A/G]GACTACAGGAGTGCA | 10138 |
rs562930044 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | YAF2 | GRCh38.p7 | 12:42168742 | AAGCAGAATCTACTA[C/T]ACAAACTCTAGATCT | 10138 |
rs562935305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42174467 | AGTTTCATTTACTGA[C/T]TCCCTTCCAGTGTCC | 10138 |
rs562959982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42210112 | CAACTAAATGTATAA[C/T]TTTTTAGAAGCAGCT | 10138 |
rs562977341 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42236783 | TATATTTAATTCAAA[C/G]GGTACCTTCGTATAA | 10138 |
rs563031036 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42215287 | ATATGAAATCCAGTG[C/T]AGGCTGGGTGCAATG | 10138 |
rs563066708 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42213313 | AACCACATGAGTGAG[A/C]TTGCAAATGGATCCT | 10138 |
rs563092295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42217522 | ATAATAAAGGGGCTT[C/T]TGCAGTTCATTTTTA | 10138 |
rs563110455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42212618 | TAAAATCATTCTACA[C/T]AATCAAATTCAAAAT | 10138 |
rs563198855 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42159595 | TGTATTTAATAAGAA[A/G]CCAATTTGACTGATT | 10138 |
rs563202998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42205480 | TCCTGTGTTCAAGCA[A/G]TTCTCTGCCTCAGCC | 10138 |
rs563234910 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | YAF2 | GRCh38.p7 | 12:42180253 | AAAATTAGCTTACTA[A/T]AACACTCTAGCTTCT | 10138 |
rs563261990 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42236788 | TTAATTCAAAGGGTA[A/C]CTTCGTATAAGAATC | 10138 |
rs563310695 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42159718 | GAAAACAATGATAAA[A/G]CTATCATTAAGTTAA | 10138 |
rs563312463 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42217965 | TAAAATGGCACAGTG[G/T]CCTAAAAAAGACCAT | 10138 |
rs563338829 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42196650 | CAACAAGGACTGTGG[A/C]AAGCAAAAGCCCCAA | 10138 |
rs563385475 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42158462 | TACTGAGTGACCAGT[A/T]TGTGTCAGATAATTA | 10138 |
rs563396579 | snp | C/T | 1.72436e-05 | 0.00293624 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160546 | TAATCTGTGTATTTG[C/T]ATGGTAGGACAGAAG | 10138 |
rs563564093 | in-del | -/AAAAC | 0.00358779 | 0.0422022 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42161344 | GCTCTTCTTAAGGGA[-/AAAAC]AAAACAAAACAAAAC | 10138 |
rs563591198 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42181140 | GTTACAGCACATTCA[C/G]AGTGGGACAAGCTGT | 10138 |
rs563593998 | in-del | -/AAAG | 0.00121581 | 0.0246257 | intron-variant | YAF2 | GRCh38.p7 | 12:42171517 | TTTAAATTAAAAAAA[-/AAAG]AAAGAAAGAAAGAAA | 10138 |
rs563636864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42197248 | CCCAGTGTTCTTTCT[A/G]GACTGGTGTTCTTCC | 10138 |
rs563638000 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42222972 | CATTGGTAGTTTCTG[A/G]TGTTGGAAACTCAGT | 10138 |
rs563661374 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | YAF2 | GRCh38.p7 | 12:42201820 | CAAGTGAACCATCTG[C/G]CTTGGTCTCCCCAGA | 10138 |
rs563707426 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238472 | CCGGCGGGCGGTGCG[A/G]GGGTGGCCGCGGTGG | 10138 |
rs563726461 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | YAF2 | GRCh38.p7 | 12:42194482 | AAACCCGTCTCTACT[A/G]AAAAAACAAAAATCA | 10138 |
rs563729093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42187219 | TGGAGTGCAGTGGCA[C/T]AATCATAGTTCACTG | 10138 |
rs563817332 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42186642 | AGATCATGCCATTGC[A/T]CTCTAGCATGGGTGA | 10138 |
rs563831243 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | YAF2 | GRCh38.p7 | 12:42212063 | TCTTTAACCATTTGT[C/T]ACCTATTGACACACC | 10138 |
rs563833564 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239055 | TTGAAAGAAACCCCT[A/G]TATACTCATAAGTCC | 10138 |
rs563846018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42230321 | GAAAGAAAAAGTACC[A/G]TATGATAAAAATAAT | 10138 |
rs563904143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42195730 | ACACTGTAGAGAATA[A/G]ACCATCGAACCAGTC | 10138 |
rs563916723 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42187873 | GTCATAAAAGACATT[C/G]TGACTTTCATCCTGT | 10138 |
rs563923801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42193512 | GGCATTGTTGTTTTT[A/G]GTTTTTGTTGAGACA | 10138 |
rs563952066 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232496 | TGTGAGTCCTCTTAC[A/C]GGACAAAAAACAAAC | 10138 |
rs564045276 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157793 | ACATATATATATATA[C/T]GTATATTCAAATTTT | 10138 |
rs564048023 | snp | C/G | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42185226 | GAACTAGAATTAGTG[C/G]AACAAGAAGATGTGA | 10138 |
rs564121799 | in-del | -/AGA | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42196128 | TCAGGAGGCTGAAGC[-/AGA]AGAACTGCTTGAGCC | 10138 |
rs564123437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42178880 | TTGGAATCATCTGAG[A/G]AGCTTTAAAAAAAAA | 10138 |
rs564188746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42229948 | ACCAAGGGGTGGAGG[A/G]ATGGTAATCCTAGAG | 10138 |
rs564225926 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42213643 | AATAACTTTTTAAAA[C/T]AGAAATTCCTCTATT | 10138 |
rs564245589 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42215227 | GTTCTAAATAACTTT[G/T]TTATTCAGCACTCCT | 10138 |
rs564273355 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42218869 | GAAGATGAGTGGGGG[C/G]AAAAAAGGAAAGATA | 10138 |
rs564285137 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42214433 | CATGCTACCATGCCC[A/G]GCTAATTTTTATACT | 10138 |
rs564301379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42207267 | CAAACTGCTTTCTGA[C/T]GATTATTTAGAAGAG | 10138 |
rs564364735 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | YAF2 | GRCh38.p7 | 12:42207708 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT | 10138 |
rs564405247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42221324 | ACACCTGTAATCTCA[A/G]TACTTTGGGAGGCTG | 10138 |
rs564412144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42166033 | AAGCGATTCTCCTAC[C/T]TCAGCCTCCCGAGTA | 10138 |
rs564419939 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42208454 | AAATAAAAATTAAAT[A/T]AAATTAAATTAAAAT | 10138 |
rs564444146 | snp | A/G | 0.000772399 | 0.0196368 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42237582 | CCGGCGGCGCGAGGG[A/G]CAGGCCCGGGACTCA | 10138 |
rs564448133 | in-del | -/AAGA | 0.00119928 | 0.0244582 | intron-variant | YAF2 | GRCh38.p7 | 12:42230290 | AAAGAGAAGAAAGAG[-/AAGA]AAGAAAGAAAGAGAA | 10138 |
rs564450609 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42216373 | AAGATTCTGTCTGAT[C/G]AAAGTAAAAGCCATT | 10138 |
rs564508483 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42225694 | GATGGTTGTAGATAC[A/G]TGGTGTTATTTCTGA | 10138 |
rs564583660 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | YAF2 | GRCh38.p7 | 12:42162159 | CAGAGAAGGAAATAC[C/T]TGACCATTTGTGACA | 10138 |
rs564663506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42200908 | GTTATTTACCCCTCT[A/G]TATTTCAGTATTCCC | 10138 |
rs564691538 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42208359 | TGAACCTGGGAGGCG[A/G]AGGTTGCAGTGAACG | 10138 |
rs564696636 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239229 | CTTCTACCTCCCCAA[C/T]GTATTCAGTAATCCA | 10138 |
rs564727025 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | YAF2 | GRCh38.p7 | 12:42200321 | GCATGTATCAACTGA[A/G]TCAAAATTATTTTCC | 10138 |
rs564742720 | in-del | -/AAGAAAGAG | 0.0184095 | 0.0941585 | intron-variant | YAF2 | GRCh38.p7 | 12:42230263 | TCCTTCAAGAAAGAA[-/AAGAAAGAG]AAGAAAGAGAAGAAA | 10138 |
rs564748291 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42156882 | GTGCTAAGAAGTCAA[A/C]GCGTTCTTTTACTAT | 10138 |
rs564753738 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | YAF2 | GRCh38.p7 | 12:42183313 | GAGGAAGAGGCATAC[A/C]TCTCTCACTTTAAAT | 10138 |
rs564792413 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42183974 | AGACCCTTTGAAATT[A/T]TGCTAAATATACTCT | 10138 |
rs564825229 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | YAF2 | GRCh38.p7 | 12:42212564 | GAATAAATGAAAGAA[A/T]ACAAAACAAACAAAA | 10138 |
rs564829961 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42202613 | CTTTGTCATTGTATA[C/T]AGTATTTCAATCTAA | 10138 |
rs564915257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42205348 | GCTTTGACTGATCAC[A/G]ACATTGTTTTTCTTG | 10138 |
rs564926772 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | YAF2 | GRCh38.p7 | 12:42222119 | ACCGTCTTAACAACC[-/T]ATGAAAGCCAATAAA | 10138 |
rs564986814 | snp | C/T | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42176859 | GTAATCCCAGCTACT[C/T]GGGAGGCTAAGGCAG | 10138 |
rs565109622 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42235761 | CTTAGATGTACTGGT[A/T]AAAAAAAAAAATGTC | 10138 |
rs565173172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42236376 | TTAAATTTAGCATAC[A/G]TTTGAAAGTTTGCTT | 10138 |
rs565194121 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42227676 | AGTGAGGAGCCTCTC[C/T]GCCCGGCAGCCACCC | 10138 |
rs565241531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42161318 | TGTTGAAAACCACTC[C/T]TGGTTCAAATAGCTC | 10138 |
rs565331053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42175269 | AAAAAAATACACACT[A/G]TATGATTCCATTCAC | 10138 |
rs565371169 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42214316 | TCTGGCTTTTGTCCA[G/T]GCTGGAGTGCAGTGG | 10138 |
rs565471962 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42182661 | AAAATACACTTCCCA[C/T]ACTCAATGAGGTCAG | 10138 |
rs565504703 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42176106 | ACAAAATTTGCCAAA[C/T]GTGGTGGTGTGCATC | 10138 |
rs565540937 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | YAF2 | GRCh38.p7 | 12:42168698 | CTCCATTCACAGGAA[C/T]AAGCCACTGTTCTCA | 10138 |
rs565545587 | snp | A/C | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239749 | TGCGGTCGCTCACGC[A/C]TGTAATCCCAGCACT | 10138 |
rs565551077 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | YAF2 | GRCh38.p7 | 12:42211495 | TAATCCCAACACTTT[C/T]GGAGGCCAAGGCAGG | 10138 |
rs565582541 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239777 | ACTTTGGGAGGCCGA[A/G]GCGGGCGGATCACCT | 10138 |
rs565625887 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | YAF2 | GRCh38.p7 | 12:42208583 | AAACACTAGCCAATA[A/G]GGGTATTAACTGGGT | 10138 |
rs565636594 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42222780 | CTTTTCTTTCAAAAG[C/T]ATTGTTGAGAAGATT | 10138 |
rs565646091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42208147 | AAAAATAGCAATATG[A/G]CCAGGCGCCATGGCT | 10138 |
rs565646160 | in-del | -/AAGA | 0.00319169 | 0.0398203 | intron-variant | YAF2 | GRCh38.p7 | 12:42230293 | AGAAGAAAGAGAAGA[-/AAGA]AAGAAAGAAAGAGAA | 10138 |
rs565671437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42165278 | AATAACTTCTGTCCA[C/T]GTTTAAATGGTCAGT | 10138 |
rs565682254 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42202077 | TGGAATTTATTTTCA[A/C]GTATTGCTTGAAGCA | 10138 |
rs565708209 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42165816 | TAACTAACTCCTCAT[C/G]AACTGTCATGCCTAA | 10138 |
rs565749931 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42208657 | CTTACAGACATCCCA[C/T]TTTTCTACTGAAGAA | 10138 |
rs565854872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42231856 | AACATATAGTATCAA[A/G]TGTTTTCCTTGAAGT | 10138 |
rs565869084 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42185429 | AGCAACAGGGCTTGA[A/G]AGGACTGGCTTAAAT | 10138 |
rs565902409 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42195355 | AAATTGTGGCATTAA[A/T]CATAACTTCAATTTA | 10138 |
rs565904174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42186738 | CACTAGGAGTAACCA[A/G]GAAGCAGATTAGTAT | 10138 |
rs565909393 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42172067 | TTATTCTTCCAATGC[G/T]CTATGCTCTTTCTAT | 10138 |
rs565950544 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42213835 | AACAGTAAGGTACAA[A/G]CTCATTCTCTTTTAT | 10138 |
rs566039401 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42215345 | GGAGGCTGAGGTGGA[A/T]CGCAAGAGCCCAGGA | 10138 |
rs566061339 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238586 | CTCGCGCTCCAGAGC[C/T]CCTCTGAGGAGGAAA | 10138 |
rs566159710 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42179082 | AAAAAATACACTTGT[C/T]TGGGCTCCACCTTTA | 10138 |
rs566186862 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | YAF2 | GRCh38.p7 | 12:42229528 | TGTAGGGCAGATAAG[C/T]GTCTAGACAATTATA | 10138 |
rs566188110 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42170014 | TAACTGGTACCACAG[G/T]CACGCATCACCACAC | 10138 |
rs566378800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42236613 | TTTAGAAATCTAACG[C/T]CTACTGAATATTTGT | 10138 |
rs566403053 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42177588 | TACCAGCCTTATCTC[C/G]AAATACAGTCACATA | 10138 |
rs566442076 | snp | A/C/G | 0.00557542 | 0.0525036 | intron-variant | YAF2 | GRCh38.p7 | 12:42227733 | CCCGGCAGCCACCCC[A/C/G]TCCGGGAGGGAGGTG | 10138 |
rs566471297 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42226590 | GACCACTTCAACCTG[A/G]GAGGTTGAGGCTGCA | 10138 |
rs566501829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42218932 | GAAAGAAAGCTTCAA[A/G]TCTCTCCTGCCACCC | 10138 |
rs566570884 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42219972 | GTTCCCTGGTAAAAT[A/T]AGACTGAGAACTGCT | 10138 |
rs566640911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42214022 | GCAGCCTGCCAGTCC[A/G]TTCTCCTTACAGAAG | 10138 |
rs566693263 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42169835 | AGGGTTAGAGATATA[C/T]AGTAGAAGAGTTTCC | 10138 |
rs566697985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42207631 | GGCACGGTGGCTCAT[A/G]CCTGTAATCCCAGCA | 10138 |
rs566740024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42206693 | TCCATTATAAATCAC[C/T]TCTTTAATGACAAAA | 10138 |
rs566749109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42176338 | GCTGGCCAGACTGGT[C/T]TCAAACTTCTGGCCT | 10138 |
rs566752641 | in-del | -/T | | | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42161379 | AAATCCAGACACAAA[-/T]TGTCTTCCAATCTCG | 10138 |
rs566758870 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42214608 | TGATTAAATGCCACC[C/G]ACTCAGAGAAGCCTC | 10138 |
rs566804265 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42199772 | ACTGTACTATTCTAA[C/T]ATTAAAAGACTATTA | 10138 |
rs566860146 | in-del | -/AAC | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42200499 | ATAAATGAAGATTAA[-/AAC]AACAAAGGTCAATCT | 10138 |
rs566909142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42205669 | TGAGCCACCGTGCCC[A/G]GTCATTGCTGATTAT | 10138 |
rs567001014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42204934 | TAGGAGAGATGAAAA[C/T]GTTCTAAAAATGACT | 10138 |
rs567060069 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42200715 | TAAGTGTGGGTAAAT[A/T]AGATCACATTGTACA | 10138 |
rs567088888 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42190629 | TCATTTTCTAGTAAT[C/G]AAATTCTTAGAAATA | 10138 |
rs567174343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42236067 | GAAAATAGAGAGGGA[A/G]CAACAAAAAGCAATA | 10138 |
rs567222448 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42225852 | CTTAGGACTGTTTTG[C/G]GTATACAGGCTCTTT | 10138 |
rs567279976 | snp | A/C | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42235397 | AAAAATATTAATATT[A/C]TGTGATGCAATCAAT | 10138 |
rs567367265 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42231019 | AAGTAAAGCCATTGC[A/G]TGTAGAAACCCAAGC | 10138 |
rs567381921 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42173309 | GCAGACCAGAACACA[A/G]TTTTCCCCCAACTCC | 10138 |
rs567516341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42173934 | AGTCTGACTTCCCTA[C/T]CCTTACTCTTAATTA | 10138 |
rs567523417 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42175497 | ACTTAACATATTGCA[G/T]GTTTTATGTGTGGTT | 10138 |
rs567544191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42186625 | GAGGTTGCGGTGAGC[C/T]GAGATCATGCCATTG | 10138 |
rs567551456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42166331 | TCTTGAAGAGACAGA[C/T]ATTCTCTCTGCTTCA | 10138 |
rs567622196 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42200901 | TGAGTAGGTTATTTA[C/T]CCCTCTATATTTCAG | 10138 |
rs567635174 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42200805 | CAAAAGGTAGCATGG[C/T]ATAGTGGACTCTGAA | 10138 |
rs567655060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42187287 | TCAGCCTTCCAAATA[A/G]CTGGTACTACAGGTG | 10138 |
rs567663892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42202708 | CAATGGCATGATCTC[A/G]GCTCACTGCAACCTC | 10138 |
rs567671914 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42214116 | TGTCATATCATTTAC[A/G]ACTAAATTGTGATCT | 10138 |
rs567684514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42222927 | GCTTATAATTTATTG[C/T]TGCCAAATTCTTTTT | 10138 |
rs567760842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42231742 | ATTGATACCACCACT[A/G]ATCTTCTCAGAAAAG | 10138 |
rs567771454 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42224438 | AACCTCCAGGTTTGT[C/T]ACATAGGTATACACG | 10138 |
rs567849313 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42169998 | ACCTCAGCCTCCAAA[C/G]TAACTGGTACCACAG | 10138 |
rs567897673 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42172451 | CATGTGTGATACAGT[A/G]GTGGATGAATTTAGA | 10138 |
rs567936799 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42217569 | ACACTGTGATGGGCA[C/T]TGAGAATTTTAAAAA | 10138 |
rs567960650 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42159889 | AATTATAAAGCTAAA[C/T]AATCAATGTTTTATT | 10138 |
rs567991096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42210204 | GCTCAGTATTTACTG[C/T]CCACACAATAATTTC | 10138 |
rs568040175 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42215302 | TAGGCTGGGTGCAAT[G/T]GCTAACACCTGTAAT | 10138 |
rs568084486 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42164844 | GGAGGCCAAGGCAGG[A/C/T]AGATCATTTGAGTCC | 10138 |
rs568097173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42172305 | ATAAAGGACAGAAGT[C/T]GTACAAAATTATAAA | 10138 |
rs568103896 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42207869 | GCACTCCAGCCTGGG[C/T]GACAGAGCGAGACTC | 10138 |
rs568145301 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42180365 | CAGGTCATCAGGAAC[G/T]AATGTCCTAGGTCCA | 10138 |
rs568209554 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42186950 | AGCGAACTATAATTT[C/T]AAATTAGCATAGGAG | 10138 |
rs568214650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42201212 | CCTCCTTGGGCAACT[A/G]TTCAAGTTTCTCTAG | 10138 |
rs568250489 | in-del | -/CAAA | 0.0651021 | 0.168264 | intron-variant | YAF2 | GRCh38.p7 | 12:42185176 | AGCCAGACTTTGTCG[-/CAAA]CAAACAAACAAACAA | 10138 |
rs568287665 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239731 | TAACATTTTTTGGCC[C/G]GTTGCGGTCGCTCAC | 10138 |
rs568293412 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157905 | GATTACTGGCATGAG[C/T]CATCACACCCGGCCT | 10138 |
rs568328461 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42223873 | CACACTGGGGCCTGT[C/T]GGGGGGTGGGGGGCA | 10138 |
rs568392830 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42194705 | TTTTTTGGTGTTGTA[C/T]AGTTACTCACTCACT | 10138 |
rs568403559 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42229495 | GGAATACCAAAGTGA[A/G]TAAGACGGTCTCTGC | 10138 |
rs568563267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42185326 | AGTGGTTTCTTGATA[C/T]GGAATCTACTCCTGG | 10138 |
rs568572007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42176538 | AACACTTAGAAGCAG[C/T]ATTTATTCCGTTTTT | 10138 |
rs568586864 | snp | A/C | 5.37793e-05 | 0.00518525 | intron-variant, synonymous-codon, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42237721 | CTTCGGCTGCCGCTT[A/C]GGCCTGCAGGACACA | 10138 |
rs568747666 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42163140 | CTAGTTTCCAAGTTA[C/T]GCTGATGTCTCTGGG | 10138 |
rs568761402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42191249 | TTTGTGCTTCATCTT[C/T]AAAAGGTAAAGATCT | 10138 |
rs568784417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42170435 | GATAACAAAGAATAC[C/T]TGATATCTGTGTTGG | 10138 |
rs568791161 | in-del | -/AAAT | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42167309 | CTTACAGTAAAATAA[-/AAAT]AAATAAAATAGTTCC | 10138 |
rs568820598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42183420 | GCCAGTTAGCTAAGA[C/T]GTGACTATAAAGAAA | 10138 |
rs568824285 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42190393 | TTAATACTGTTTATA[A/T]CTATAGTTACTTCTT | 10138 |
rs568879034 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | YAF2 | GRCh38.p7 | 12:42225730 | CTGTTCTGTTCTATC[A/G]GTCTATATGTCTGTT | 10138 |
rs568897589 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42235229 | TGCAGCTATCCAGTC[G/T]TGGCTTTAGTACTTG | 10138 |
rs568963303 | snp | A/G | 0.000162272 | 0.00900608 | intron-variant, synonymous-codon, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42235871 | ATTCCTTCTTCTTCC[A/G]GGTGCCAGGTATTCA | 10138 |
rs568963343 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42226527 | AAATTAGCCAGACAT[A/C]GTGGCACACCCCTGT | 10138 |
rs568973527 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42226911 | GGGGTCGGTGGCTTA[C/G]GGAGCCCGTCCGGCC | 10138 |
rs568997047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42219725 | ACCTCATTATCTTAT[C/T]CAGAAAAAATACAGC | 10138 |
rs569001120 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42229702 | ACAGCCTACTACATA[A/C]CTAGGCTATATGGTA | 10138 |
rs569007468 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157616 | TATCAACTTAGAAAG[A/G]CTGAAGTTTCTCTTC | 10138 |
rs569066917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42163683 | ATTCTATGATTATTT[C/T]ATCTGGTTCAATTCT | 10138 |
rs569073716 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42196797 | AAATTTCTTTGAAAC[A/G]TGGTGCAGGCTAACA | 10138 |
rs569099805 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42213880 | CAAACAGGGGTACTA[C/T]ACAGACCTCCATTTC | 10138 |
rs569112198 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42194239 | TTTATAAAATCTACA[A/G]TGGCATACAGTAATT | 10138 |
rs569113494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42212965 | TAAGTACATAGCACA[A/G]AGGTCTTATATGTTT | 10138 |
rs569149475 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42190594 | TTCTTGTATTAAATT[A/C]TTTTGTTGAGTGTTT | 10138 |
rs569158142 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42186685 | TCCATCTCAAAAAGG[-/A]AAAAAAGAAAGAAAA | 10138 |
rs569272996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42174829 | AATTTTATAAATAGA[A/G]TATTTGTAAAAATAA | 10138 |
rs569286156 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42168065 | CAAATATATCTTGAT[G/T]GCATAATATTTTTAA | 10138 |
rs569286913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42175342 | GCAGATCAGTAGTTG[C/T]CTAGCAACCAGAGAT | 10138 |
rs569314886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42218327 | CAACCACAATGATAT[A/G]CAAGTATACATTTCC | 10138 |
rs569326031 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42202569 | AAGTCTGGGAGAGAG[A/T]CATCCCATGTTATGC | 10138 |
rs569399154 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42179385 | TGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGA | 10138 |
rs569438061 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42226425 | CCCAACATTTTGGAG[A/G]CCAAGGTGAGAGGAT | 10138 |
rs569460549 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42208469 | TAAATTAAATTAAAA[G/T]TTAAAAATAGCAATA | 10138 |
rs569485876 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42204793 | ATAAACCTTAAACAC[A/T]TGCTAAGTGAAAGAA | 10138 |
rs569489475 | in-del | -/CTTGCGTAATGATCAGA | 0.00597247 | 0.0543191 | intron-variant | YAF2 | GRCh38.p7 | 12:42181451 | CCAGAGCTGTTACTT[-/CTTGCGTAATGATCAGA]TCTGTGGCTCTTTGA | 10138 |
rs569533361 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42211699 | GCAATGAGCCAAGTC[A/G]TGCCATTGCACTCCA | 10138 |
rs569543088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42231972 | TCAAGTAAAAATGAT[A/G]CTCTATGACAAAAAG | 10138 |
rs569598104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42197601 | TGCATGTGAGATTCC[A/G]CTGGAATAGAGGTGG | 10138 |
rs569604800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232845 | ACTCTTTTTACCTAA[C/T]CATAATAATAATACT | 10138 |
rs569619247 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233662 | GACCACAGGCATGCA[A/C]CACCACACCCAGCTA | 10138 |
rs569677340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42195424 | AGATTTCTAAAAAGT[A/G]TTACCAGAATTTAAA | 10138 |
rs569695063 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42158780 | TCATTTAAAATACAT[C/G]CTGAAAGTTATTTGA | 10138 |
rs569809119 | in-del | -/TACT | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42236324 | AATCATTTTAGCAAA[-/TACT]TTTTTTCTTTTTGGA | 10138 |
rs569822474 | snp | C/G | 0.0008 | 0.019984 | intron-variant | YAF2 | GRCh38.p7 | 12:42196032 | TTGGAGACCAGCCTG[C/G]CCAACATGGTGAAAC | 10138 |
rs569851051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42186468 | ATCACCTGAGGTCAG[A/G]AGTTTGAGATCAGCG | 10138 |
rs569852919 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42179170 | TGAAGTTTCCAAGAT[G/T]ATTCTAATGTGCAGT | 10138 |
rs569853619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42225136 | GACCAGTGATGAGTT[C/T]TTCACATTTGTTGGC | 10138 |
rs569889195 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42180827 | GTGGTGCGTGCCTAT[A/G]ATCCCAGCTACTCAA | 10138 |
rs569891648 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42179780 | TGAAGTGAGACCCTG[C/T]CTAAAAGGCAAAAAA | 10138 |
rs569927696 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42181473 | AATGATCAGATCTGT[C/G]GCTCTTTGAATAACT | 10138 |
rs570030260 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42187361 | GATGGGGTTCTGTTA[C/T]GTTGCCCAGGCTGGT | 10138 |
rs570037922 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42175027 | ATTTCCCTTTCAATA[C/T]ATGTACTCAAAGAAG | 10138 |
rs570040359 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42196210 | CCAGCCTGGGCGACA[A/G]AGCAAGAATCCATCT | 10138 |
rs570052950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42208624 | TACTGTATTAAATAA[A/G]TTCCATGAATTAATA | 10138 |
rs570093992 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238750 | GACTTTCCTGGCCTC[C/T]GCTGTCCTTAGCTAC | 10138 |
rs570119127 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42223680 | GTGCTTTATTAATAA[G/T]GGCCACATGCAGCCA | 10138 |
rs570154370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42216089 | TATAATCTAAAGTCA[C/T]TGTTAGAGGCATAGA | 10138 |
rs570155748 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239397 | AGGAAAGCTGCCTCC[C/T]GACAAAGAGTGCAGA | 10138 |
rs570155760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42230178 | AGGAGAATCGCTCAA[A/G]TCTGGGAGGCGGAGA | 10138 |
rs570166297 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42230768 | ACAAAGTAAAGAATA[C/T]ACAGATGCCAAGTTT | 10138 |
rs570190044 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42216027 | GACACCAACAAGTAC[C/T]CAATGTTTTGGGATT | 10138 |
rs570320406 | snp | C/G | 0.0501905 | 0.150254 | intron-variant | YAF2 | GRCh38.p7 | 12:42229221 | GAAGGCAGCATGCTC[C/G]TTAAGAGTCATCACC | 10138 |
rs570343725 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42156647 | TCATTGCCTGTGATA[A/G]GAGTGGGGCTTACTT | 10138 |
rs570369084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42216754 | AGATCTTCCCTCTCA[A/G]ATTTTCCCCAGGCAC | 10138 |
rs570403290 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42171216 | AGGCTGGTCTCAACT[C/G]CTGACCTCAAGTGAT | 10138 |
rs570440055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42170796 | GACTGCAGTGAGCCG[C/T]GATTGTGCCACTGCA | 10138 |
rs570478817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42163834 | TCTTTTTACAACATC[A/G]TAAGTCACTCAACTC | 10138 |
rs570486352 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42205069 | TTAAAAAAAAAAAAA[A/C]CACCTATTCCTCTTG | 10138 |
rs570540894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42214150 | ATTTTACCCACTTGC[C/T]CACCTTCATCTGATG | 10138 |
rs570558423 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42215463 | AGAGATAGCTGTTAC[C/T]TTATAGAACAAATGA | 10138 |
rs570596764 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42205738 | TCCTCTTCTTCCTTT[G/T]GCTCTACTCTTTTTT | 10138 |
rs570744911 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | YAF2 | GRCh38.p7 | 12:42207847 | AGTGAGCCGAGATCG[C/T]GCCACTGCACTCCAG | 10138 |
rs570762472 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42191277 | TCTGTGGCCCTCTTT[A/C]TATTAGAAACTATAC | 10138 |
rs570803188 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42236723 | TGGACTTTGTAATAT[C/G]AAAATACATATCTTC | 10138 |
rs570887877 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | YAF2 | GRCh38.p7 | 12:42162682 | TTTTAAAAAATCTTT[C/T]TTTCTCCTGTTCCTC | 10138 |
rs570910049 | in-del | -/TATC | 0.0360663 | 0.129354 | intron-variant | YAF2 | GRCh38.p7 | 12:42165884 | TTTAAATTCTATCTA[-/TATC]TATCTATCTATCTAT | 10138 |
rs570954543 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42219769 | CTTTAATGTGCATAT[A/T]AATAACCTAAAGATC | 10138 |
rs570978828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42192295 | GGAGGATCTCCTGAG[C/T]CCAGGAGATCAAGAC | 10138 |
rs571050053 | snp | C/T | 0 | 0 | intron-variant | YAF2 | GRCh38.p7 | 12:42182367 | AGTTGGAACAAAACA[C/T]AAATGTGAAAAAAAA | 10138 |
rs571129514 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | YAF2 | GRCh38.p7 | 12:42227764 | GGGGGGTCAGCCCCC[C/T]GCCTGGCCAGCGTGC | 10138 |
rs571201716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42184560 | GGTGATTGACTCACC[A/G]CAGCCTCTCAAAGTG | 10138 |
rs571244103 | in-del | -/TAAATAAATAAATAAA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42215963 | AAATAAATAAATAAA[-/TAAATAAATAAATAAA]GCTACTGTACATTTA | 10138 |
rs571268064 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42206017 | AATTAGACCTATATT[A/G]GAACTGCTCAATCTA | 10138 |
rs571330345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42175591 | TAATCAAATTAAAAC[A/G]GGAGGCCAGGCACGG | 10138 |
rs571348435 | in-del | -/TTATC | | | intron-variant | YAF2 | GRCh38.p7 | 12:42188020 | CTGCAGCCTCAGCTG[-/TTATC]TTAGTTGCACCCTCA | 10138 |
rs571356826 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42202003 | TATCCTAAAGTTGCA[C/T]ACTCATCTATACTAT | 10138 |
rs571356913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234032 | AAAAATTAGCCTGGT[A/G]TGGTGGCGGGCACCT | 10138 |
rs571385200 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42235172 | CAAATCCCATCTGTG[C/G/T]GTCACACAAACAAAT | 10138 |
rs571421344 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42203063 | CAGGAAGGTCATTTT[C/T]CACAAAAAAAAAAAA | 10138 |
rs571435924 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42223314 | CATCTTAAAAACAGC[A/G]GTTTCTTTAAAATAC | 10138 |
rs571451993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42226453 | GATTGCTTTGGCCCA[A/G]GAGTTCGAGACCAGA | 10138 |
rs571474269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42169231 | GTGTATCATGACATT[A/G]TTTAACATTCTCCTG | 10138 |
rs571498450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42167397 | TCCCGTTATATATGA[C/T]AGAAATATAAAAGGG | 10138 |
rs571530077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42180606 | TAAGTTCCGGGTAAT[C/T]TGTTATGCAGCAGTA | 10138 |
rs571537088 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42159956 | ATGTTTTGAAAAATA[A/G]GCAAACAAAAAAACC | 10138 |
rs571567440 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42174019 | CTGACCTCCTTTGTT[C/T]CCTGCTTAAACAATA | 10138 |
rs571574628 | snp | C/T | 1.6625e-05 | 0.00288309 | synonymous-codon, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160721 | AGCACTAGATGCAGG[C/T]GGTGACTTTGTTTTC | 10138 |
rs571635031 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42207885 | GACAGAGCGAGACTC[C/T]GTCTCAAAAAGACAA | 10138 |
rs571646567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232762 | ATTTCTACCAGATGA[C/T]AGTTGGTTTAAGCTT | 10138 |
rs571668819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42174691 | ACTCCTCTTGTTGAC[C/T]TCATTCAGTCCTCGG | 10138 |
rs571763839 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238433 | AAACGCGGCCAGCGC[G/T]GCCCAGCACCCGCGG | 10138 |
rs571765500 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42216936 | ACTTCCTGCCTCCCA[C/T]AACCATATCCAATCA | 10138 |
rs571827251 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238931 | CTCAAGAGAGATTAG[A/G]TGACTTCCTCTAGGC | 10138 |
rs571856874 | in-del | -/AGTCCA | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42213105 | TCCCAGCACTTTGGG[-/AGTCCA]AGGCGGGCCTTTCTC | 10138 |
rs572004444 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42236485 | AGCATGTCAAAACCA[A/G]CGAGCTTCACTGAGA | 10138 |
rs572059558 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42156822 | TTTCCTACATTCTTT[C/G]TTCCAGACAACTGAA | 10138 |
rs572079912 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42224711 | AGGACATGAACTCAT[C/T]CTTTTTACAGCTGCA | 10138 |
rs572112060 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42184829 | TCATGGATGACTGAA[C/T]GGTTCAAGATTTCAG | 10138 |
rs572150135 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42179315 | TCTCTACTAAAAATA[C/G]AAAAATTAGCAGAGC | 10138 |
rs572155618 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42193393 | AATAAATGACTGTTA[C/T]TAGTTTATGTATTTA | 10138 |
rs572176619 | in-del | -/T | 0.0379877 | 0.132479 | intron-variant | YAF2 | GRCh38.p7 | 12:42170990 | TCAGGAATTGTTTAG[-/T]TTTTTTTTTGTTTTT | 10138 |
rs572176926 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42230271 | GAAAGAAAAGAAAGA[A/G]AAGAAAGAGAAGAAA | 10138 |
rs572228594 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42221242 | AGAAGTTACTTGCTA[C/G]CAAATTTAATTAAAT | 10138 |
rs572231091 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42186143 | TTGCAGTGGCTGAGA[C/T]TGCGCCACTGTACTC | 10138 |
rs572242299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42223246 | CATATAGCGCCAGCA[C/T]ACTATGTAGGAAGTT | 10138 |
rs572263028 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42231255 | TTTTAAAAACTTATT[A/C]TTTTCCAAAACAAAG | 10138 |
rs572337299 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | YAF2 | GRCh38.p7 | 12:42222120 | ACCGTCTTAACAACC[A/T]TGAAAGCCAATAAAC | 10138 |
rs572337571 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42214380 | GGGCTCAAGCCATTC[A/T]CTTACCTCAGCCTTC | 10138 |
rs572387835 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42236319 | ACCACAATCATTTTA[C/G]CAAATACTTTTTTTC | 10138 |
rs572394398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42237015 | AACTAAAGATATAAA[A/G]GTACTTTCAGTAAAA | 10138 |
rs572400357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42214832 | AACACGGCGAAACCC[C/T]TTCTCTACTAAAAAT | 10138 |
rs572449179 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42227637 | GTTAGGAGCCCCTCC[A/G]CCCAGCAGCTGCCCC | 10138 |
rs572466661 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42209157 | TTTCATTACAAACAA[C/G]GAAGCGGTAAATAGA | 10138 |
rs572476711 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42159379 | GTACTGTGTGGTTTC[C/T]AGGTTGAAATTCTAA | 10138 |
rs572553805 | snp | A/G | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233748 | AAACTCCTGGCCTCA[A/G]GAAATCCTCCTGTCT | 10138 |
rs572616746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42171454 | ATGATCATACCTCTG[A/G]ATAGCCACTGGCATT | 10138 |
rs572697196 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42162849 | GACAGTCTGAACTAC[C/T]GAAAGGATATCCAGG | 10138 |
rs572759366 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42192732 | GAATGGATTTAAAGA[C/T]TTTGGTCAAGGTAGT | 10138 |
rs572766302 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42194517 | GGTGTGGTGGCAAGC[A/G]CCTGTAATCCCAGCT | 10138 |
rs572785224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42198699 | GCTCTGTAAAATTCC[A/G]AAATGGAGAGCGGGG | 10138 |
rs572839071 | in-del | -/T | 0.084728 | 0.187577 | intron-variant | YAF2 | GRCh38.p7 | 12:42205379 | CTGCTGCTTCTTCTC[-/T]TTTTTTTTTTTTTTG | 10138 |
rs572848615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42191645 | ACACTGAGCACCTAC[C/T]ATGTGCCAAGCATCA | 10138 |
rs572907581 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42219450 | GGATAAGAGATAGGA[A/G]GTATAACAGAGAAAG | 10138 |
rs572920959 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42206090 | ATTTTTCTGCATTTC[G/T]CTGTGCTTGTCCGGA | 10138 |
rs572927096 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42221793 | CTTAGCTGAAAATCC[A/C]AACAAGAAGGTTTTG | 10138 |
rs572980374 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42213071 | ATTAAGAGCCAGGCA[C/T]GGTGGCTCAAGCCTG | 10138 |
rs573120633 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | YAF2 | GRCh38.p7 | 12:42189736 | TCTGATTAGTATTAA[-/T]TAGTATTAATTAAAT | 10138 |
rs573182223 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42163727 | CACAAAACATAAATG[C/T]ATATAGTTCAATTAT | 10138 |
rs573186926 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160359 | AATGAATAATTCAAC[C/T]ACATTTTCATGGCAC | 10138 |
rs573255836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42195564 | CAATATTCCGTAAAA[C/T]AGAAACCACATAGGC | 10138 |
rs573389567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42182538 | ATCATTGGAAAAGAT[A/G]AGCTGGAATCACAAC | 10138 |
rs573397673 | in-del | -/CCT | 0.00199481 | 0.0315187 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239371 | CCCTACCTCTGCCTC[-/CCT]CTCCCATAAGGAAAG | 10138 |
rs573419465 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | YAF2 | GRCh38.p7 | 12:42197098 | TTTCGAAAATTAGTG[A/T]CATGACAACAGATAG | 10138 |
rs573421495 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42189059 | TTCCTGTAGAGATGA[C/T]TTTTAAACTGAGCTT | 10138 |
rs573425326 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | YAF2 | GRCh38.p7 | 12:42224628 | TGAGAATACGTGGTG[G/T]TTGGTTTTCTGATCC | 10138 |
rs573430349 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234660 | AAGAATTTGAACTTA[A/G]TATTATTTAAAGAAA | 10138 |
rs573501820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42183043 | ATAAAATGTTTTCGT[C/T]ATTATTATATCTGTT | 10138 |
rs573524276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42176017 | TCTGGGAGGCCAAGG[C/T]GGGTGGATCACTTGA | 10138 |
rs573537161 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42225215 | CTTTTTGATGGGGTT[G/T]TTTTTTTTCTTGTAA | 10138 |
rs573555618 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42166976 | TCTGTTTTCTTATTA[C/T]TTTGGTCTCTTTTTA | 10138 |
rs573561761 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42180275 | CTAGCTTCTACCCTC[A/T]CTCTCTCCCCTTGTT | 10138 |
rs573567950 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42163830 | ATGATCTTTTTACAA[C/T]ATCGTAAGTCACTCA | 10138 |
rs573597322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42217848 | ACTCTGACCTAGAGA[C/T]AAAGGAATGCTTAGC | 10138 |
rs573598534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42226608 | GGTTGAGGCTGCAGT[A/G]AGCTATATCCACACC | 10138 |
rs573598683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42218570 | ACATTTTTGGGATTT[C/T]GACCTTTCAGGATTG | 10138 |
rs573601856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42231436 | ACAGATATACAGTTG[A/G]AAAGAGGTAAGTAGT | 10138 |
rs573679755 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42171629 | GGGCCAGAACTGGGT[A/G]TATAACTCCTGATCA | 10138 |
rs573706793 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42193036 | TAGCACCTACCGGCC[A/G]GGCACGGTGGCTCAC | 10138 |
rs573725047 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42180941 | CGACACAGCAAGACT[A/G]TCTCAAAAAAATAAA | 10138 |
rs573779673 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42194898 | GTAACTCTCTAATAG[C/T]TCACATGTAAATAAA | 10138 |
rs573887007 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42210779 | TAACTATATATACAC[G/T]TATCAAAGTAAATAT | 10138 |
rs573965080 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42176416 | GTAAGCAACCATGCC[C/T]AACCAACAATATACT | 10138 |
rs574040756 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42195054 | TATGATAGATACGGT[G/T]TCAGCCCTTACAGTT | 10138 |
rs574146960 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157606 | ATAAACATGCTATCA[A/G]CTTAGAAAGGCTGAA | 10138 |
rs574149356 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42208788 | AAGAAAGTGAGAAAC[C/T]ACAAACCAAGTGTAA | 10138 |
rs574208699 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42158200 | ATTAATAAAAGTAAA[A/G]TAATTTCAAGTCAAC | 10138 |
rs574318399 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42206940 | CTACCCAGATTCAAA[A/C]TTGTTAACATTTACA | 10138 |
rs574417872 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | YAF2 | GRCh38.p7 | 12:42236494 | AAACCAGCGAGCTTC[A/C]CTGAGAAATTTTTCA | 10138 |
rs574444054 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42156745 | CGTATATTCTGTAAC[C/G]TTGTCTTTTTATTCT | 10138 |
rs574445838 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42198629 | AACATCACATTTTAT[C/G]TAAAGAAATTAAGTA | 10138 |
rs574552087 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42226718 | CTACAACTTAGAGAC[A/C]AAATAGTCTGATAAT | 10138 |
rs574556879 | in-del | -/AAAA | 0.0266694 | 0.112354 | intron-variant | YAF2 | GRCh38.p7 | 12:42171510 | CCATCTCTTTAAATT[-/AAAA]AAAAAAGAAAGAAAG | 10138 |
rs574564267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42200026 | CTTTAATTTGAGAGT[A/G]ACATCTGAAAGTGCA | 10138 |
rs574594282 | snp | A/C | 0.00874735 | 0.0655527 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238299 | AGGGGGCGGGGAAGG[A/C]CGCACCGCCGCGCTC | 10138 |
rs574615391 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | YAF2 | GRCh38.p7 | 12:42227564 | GGAGCGTCTCTGCCC[A/G]GCCGCCCTGTCTGAG | 10138 |
rs574636630 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238875 | AGATGCTCTAACAAG[G/T]AGGGATTGTCAACCC | 10138 |
rs574706688 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42186068 | TGGTGGTACATGCCT[A/G]TAATCCCAGCTACTC | 10138 |
rs574727401 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | YAF2 | GRCh38.p7 | 12:42227808 | GGTGGGGGGGTCAGC[C/T]CCCCGCCTGGCCAGC | 10138 |
rs574730719 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42190908 | TTTCTACTTTTTAGT[G/T]TTTTTTTCAGCTTTC | 10138 |
rs574784077 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42183166 | GGTAAGTGTTTGTGT[A/T]CTGGCTGCTCCACTG | 10138 |
rs574789324 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | YAF2 | GRCh38.p7 | 12:42221199 | CACTAGATCTAGGTA[C/T]AGGCAAAATTATAAG | 10138 |
rs574810130 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42222430 | CAGTAATCCAACAAC[A/C]CAGGTTTCAATCTAG | 10138 |
rs574829721 | in-del | -/TAAC | | | intron-variant | YAF2 | GRCh38.p7 | 12:42217609 | AATTATCATTATCAT[-/TAAC]TAAGAAATGTGCTGA | 10138 |
rs574878615 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42182459 | CTGTTTTATCACTTA[A/C]ATCAAAACTGAAAGA | 10138 |
rs574880331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42175196 | TACTACTCAGCAACA[C/T]AAAGAAATGAACCAC | 10138 |
rs574917212 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42175828 | AGGCTCAAATTTTTT[G/T]AAAGTTCTCAAGCTG | 10138 |
rs574945609 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42188791 | GTTCACTGTTGAGAC[A/G]CTATTCACTTCAAAG | 10138 |
rs575062798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42204512 | TAGAGATCATGTAAT[A/G]CATATGGGAGAATAT | 10138 |
rs575068807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42177316 | CTTAAACAGCAGATA[C/T]TTATTTTCTCACAGT | 10138 |
rs575174093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42205312 | TTCTTGGGTATTTCC[A/G]GAATCAACTGCAAAC | 10138 |
rs575191113 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42197932 | AAAATATTAAGTCAC[A/G]TATGTTATACCTTGG | 10138 |
rs575228263 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42207717 | CTAACACGGTGAAAC[A/C]CCGTCTCTACTAAAA | 10138 |
rs575236608 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42180729 | TGAGGCAGGTGGATC[A/G]CTTGAGGCCAGGAGT | 10138 |
rs575248280 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42219243 | CAATTTGAAACCACT[A/G]GGCCTCCTGAGGGAC | 10138 |
rs575288372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42218488 | TGTTGTTTTTATCTG[C/T]TTCTCAAATAAATCC | 10138 |
rs575345177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42169279 | TTCTACTTTCTTATT[C/T]CTCTTCCTACCTTCT | 10138 |
rs575378327 | in-del | -/TT | 0.00398564 | 0.0444627 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239259 | CAACCAGATTAATAA[-/TT]TAAAATGCTGTTAAT | 10138 |
rs575384998 | snp | A/G | 5.01174e-05 | 0.00500561 | intron-variant | YAF2 | GRCh38.p7 | 12:42161813 | ATTACAACTTAAAAC[A/G]TAAGTGCTTTATGAC | 10138 |
rs575395478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42161150 | ACAATGAAATAGTTG[C/T]ACCATGGAGGAAGGT | 10138 |
rs575551435 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42172504 | AACATGAGACCTGAA[-/T]TTTTTTTTAAGCGAC | 10138 |
rs575580431 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42181857 | ATGAATGAGAAGCGT[A/C]GTAATAAGTATCTGA | 10138 |
rs575591529 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42166551 | AATGACTACTTATAT[G/T]AGAAATCATATATAC | 10138 |
rs575621208 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160068 | CAAATTCTTTATTTA[A/G]TAACAATTTTCCTAT | 10138 |
rs575630135 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42159116 | TCTTACAAAAAAGAC[A/G]GTACCACTGTGCCTG | 10138 |
rs575670671 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239085 | CTTTTTAAATATAAG[C/G]AGTTTGCATGTCCCC | 10138 |
rs575677583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42209871 | TGGCACAATCTCAGC[C/T]CACCGCAACCTCTGC | 10138 |
rs575690679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42195754 | ACCAGTCATGGTGTG[C/T]TGAGACTGGGTTAAA | 10138 |
rs575748171 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | YAF2 | GRCh38.p7 | 12:42196223 | CAGAGCAAGAATCCA[A/T]CTGGAAAAAAAAAAA | 10138 |
rs575789089 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42203045 | TGAACCTTTAATTTT[G/T]CACAGGAAGGTCATT | 10138 |
rs575920730 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42207349 | ATCTTCTAAGATATT[C/T]AAACTGCAAAAATCA | 10138 |
rs575957580 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42204160 | AGATAATGAAAAGCA[C/T]TGGTGACATTACAGA | 10138 |
rs575961163 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233317 | AACCATTTAGACCAC[A/T]GTTTGAAACCCAAAC | 10138 |
rs575962513 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42186171 | CTCCAGCCTGGGCAC[A/C]AGAGCCAAACTCTGT | 10138 |
rs576002823 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42194931 | AGATGATCACGCCTA[C/G]CTTACTGACAACACT | 10138 |
rs576016533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42185533 | GGAAGAGTTAATCAA[C/T]GTGGAAAACTTTATT | 10138 |
rs576018113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42166166 | GATCCGCCTGTCTTG[A/G]CCTCCCAAAGTGCTG | 10138 |
rs576021589 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234352 | TACTGTTTCTCTCAC[A/C]AAAGCACAATGTAAA | 10138 |
rs576021752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42225468 | TAGTTTTTCAGGACA[C/T]AAAACCTTGCCTAGG | 10138 |
rs576052799 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | YAF2 | GRCh38.p7 | 12:42178523 | CATCTCTCCCCTCTC[A/T]AAAACACTACAGCCT | 10138 |
rs576114928 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42186828 | GCTCATCAAGGGTCT[A/G]AGGGTAAAAGAAACA | 10138 |
rs576186258 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42173469 | AATCATTAAATGACA[C/T]GACAGTTTGGCATTT | 10138 |
rs576253482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42179443 | CCACTGCAGTGCAGC[C/T]TCAGCAACAAAGCGA | 10138 |
rs576287715 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42217075 | TCAAAATGGTTTCTC[C/T]GCCTCTAGCTAAGAT | 10138 |
rs576290699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42180203 | GGTGCTTCTAATAAA[C/T]AGGATACAGCAAAAA | 10138 |
rs576304547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42208193 | AACACTTTGGGAGGC[C/T]GAGGCGGGCAGATCA | 10138 |
rs576304817 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42200911 | ATTTACCCCTCTATA[A/T]TTCAGTATTCCCATA | 10138 |
rs576326369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42173544 | CAAATAGGTCACTCT[C/T]AACTTTCCCTTCCTC | 10138 |
rs576366270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42201550 | CCTCCTAGGTATGTC[A/G]CATATCTTTTAGTTT | 10138 |
rs576378549 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42209361 | TTGAGTTCATGAGTT[C/T]GAGATCAGCCTGGGC | 10138 |
rs576409513 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42209095 | GGTACCTGAGGAAAT[C/G]AGGCAGCTCAAACTG | 10138 |
rs576410052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42221340 | TACTTTGGGAGGCTG[A/G]GGCAGGAGGGGTGCT | 10138 |
rs576443215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42206224 | TCAAGATTTTAATTG[A/G]TTATTTTACATAAAT | 10138 |
rs576447848 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42222247 | AACACTAAGGTTTCA[C/T]CAACTCCTTGAATGA | 10138 |
rs576460035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42214949 | GCAGAGGTTGCAGTG[A/G]GCTGAGATGGCACCA | 10138 |
rs576491584 | in-del | -/AT | 0.00478085 | 0.0486577 | intron-variant | YAF2 | GRCh38.p7 | 12:42169829 | GTAGCAGGGTTAGAG[-/AT]ATATATAGTAGAAGA | 10138 |
rs576533558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42229606 | TGCATCATTTAATGA[C/T]GGATATGTTCTGAAA | 10138 |
rs576558316 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42164939 | TGGCCAGTAAAGGTA[C/T]GCGCCTGTAGGAGGC | 10138 |
rs576600159 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | YAF2 | GRCh38.p7 | 12:42181053 | AGCTCTGGGCAACTG[A/C]ATCTTTATATATTAC | 10138 |
rs576637939 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42214191 | TCTGCCTCACTATGC[A/G]CTAGTCTTTGCTCAA | 10138 |
rs576725051 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42210944 | CACCAGGCTATTTCA[C/T]TTTGCTGAAACAATA | 10138 |
rs576741266 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42170064 | TTTGTAGAGATGAGG[A/G]TCTCACAACGTGGCC | 10138 |
rs576878206 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234849 | GAAAATTAGCCACAC[A/G]TGGTGGTGTGCATCT | 10138 |
rs576915640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42199933 | GTGTTCTCAGTCAAA[C/T]TACCTTAGTGCCTGA | 10138 |
rs577052843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42206835 | AGAAATTGAAGCACA[A/G]TAAAGTTCTCTTTAA | 10138 |
rs577161503 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42237104 | GGAATAAAAACACTA[A/C]ATAAAACCTTGATCT | 10138 |
rs577181587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42181030 | AGGATGGCTTCTTTG[A/G]TACACCTAGCTCTGG | 10138 |
rs577253469 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42197804 | TAAATTATAGAAAAT[G/T]TGGCTGCTATTGGGA | 10138 |
rs577322772 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42190041 | ACAATTTACTTTTGT[C/T]GTTTTATTAAGATTG | 10138 |
rs577323950 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42217923 | GGAGGATGGGGAAGT[A/T]GAGGGCAGAAGAAAC | 10138 |
rs577370531 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42176681 | CTTCATAACATCCCG[G/T]CCAGGTATGGTGGCT | 10138 |
rs577383785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42218468 | GTGTAAAGTGGCCTA[C/T]GAATTGTTGTTTTTA | 10138 |
rs577461181 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | YAF2 | GRCh38.p7 | 12:42227191 | GGCCCCACGGGGCCC[A/G]AGGGCAAGGAGCAGC | 10138 |
rs577476963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42183110 | CTGTCATTGTTTTGA[A/G]GAGCCAAGGCCCACA | 10138 |
rs577494099 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42211636 | TGTAATCCCAGCTAT[C/T]AGGGAGGCTGAGGCA | 10138 |
rs577566414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42174357 | CACTTCACTGAGTTT[A/G]TCACTCCTTCCCTTC | 10138 |
rs577613308 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42212566 | ATAAATGAAAGAAAA[A/C]AAAACAAACAAAAAA | 10138 |
rs577632849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42165978 | GCTGGAGTGCGGTGG[C/T]GTGATCTTGGCTCAA | 10138 |
rs577658058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42225330 | TGTTCACTCTGATGA[C/T]AGTTTCTTTTGCTGT | 10138 |
rs577708233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42175102 | AACTTCATTTGTAAT[A/G]GCCCAAAACTGAAAA | 10138 |
rs577728753 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | YAF2 | GRCh38.p7 | 12:42178924 | CAGGTGTGGTGGTGC[A/G]TGCCTGTAGTCTTAC | 10138 |
rs577742234 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | YAF2 | GRCh38.p7 | 12:42167712 | ATAAACGAAAAGCTG[C/T]TGAAAATTTCTGGCC | 10138 |
rs577787440 | snp | A/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42231315 | TTTTTGCAAACCTCT[A/T]ACATCTGGTTAGTAG | 10138 |
rs577790224 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157320 | CTGCAAGAGCGAATC[C/T]ATTCCAGAACTAACT | 10138 |
rs577813441 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | YAF2 | GRCh38.p7 | 12:42227803 | AGGGAGGTGGGGGGG[C/T]CAGCCCCCCGCCTGG | 10138 |
rs577837843 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42203976 | GGGAAATTGCTTGAG[A/G]CCAGTTTGAAGCTGC | 10138 |
rs577841327 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | YAF2 | GRCh38.p7 | 12:42198019 | CTAGGAAAAAAAGTT[-/A]AAAAAAAAATCAGTT | 10138 |
rs577925331 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160458 | AATTCTAACAAATTT[A/C]TATTTTATGTAAAAC | 10138 |
rs577931118 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42195700 | ACACAGTTTTGCCCT[C/G]AAAAAGGCTACAGAA | 10138 |
rs577948842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42173400 | CACAGACAAAACAGA[C/T]TACTTACATCATTTC | 10138 |
rs577962755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42160993 | TTTCAACTCATTAAC[A/G]TTAATCAAACCAATC | 10138 |
rs577966165 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42187799 | TTCCCACACTGAATA[C/T]GGCTGACTTGTATAA | 10138 |
rs577983511 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | YAF2 | GRCh38.p7 | 12:42207630 | GGGCACGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 10138 |
rs578042152 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | YAF2 | GRCh38.p7 | 12:42202241 | TAGTTTGTCTTTTCC[G/T]GTACTAATACTATAC | 10138 |
rs578060917 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42237297 | CCAACATTTTTATAC[C/T]CAGAATGGGGAGAGG | 10138 |
rs578095461 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42216341 | ACAAATACTACATGG[A/T]ACTTGAGAGAAAAAT | 10138 |
rs578169769 | snp | A/G | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239846 | CGAAACCCCATCTCT[A/G]TTAAAAAATACAAAA | 10138 |
rs578171108 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42164354 | TTTGGAGCTGGCTGA[C/T]CTTCTGTGTGAGCAG | 10138 |
rs578187301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | YAF2 | GRCh38.p7 | 12:42195680 | ATTAGAAATCAAAGG[C/T]GAAGACACAGTTTTG | 10138 |
rs578259789 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | YAF2 | GRCh38.p7 | 12:42201346 | ATTGATAGCTCGTAC[A/G]TTTTCAACTGCACTT | 10138 |
rs745336846 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42204110 | CTATCCCTTCTGACA[C/T]CACTTCACACAAACT | 10138 |
rs745360852 | in-del | -/ATTATAATTGAA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42219938 | CTCCACATGATCTAT[-/ATTATAATTGAA]AAACAAAGTTCCCTG | 10138 |
rs745402581 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42169491 | CAATCTCAGCTCACT[A/G]CAGCCTCTGCCTCCT | 10138 |
rs745408201 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42225575 | TGTAAGGAAGGGATC[C/T]AGTTTCAGTTTTCTG | 10138 |
rs745469422 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42168340 | TGCACCACCATGCCC[A/G]GCTAATTTTTTTTGT | 10138 |
rs745474366 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42219700 | GGGATGAATACCTCA[C/T]ACCCCGTCCACCTCA | 10138 |
rs745505112 | in-del | -/A | | | intron-variant | YAF2 | GRCh38.p7 | 12:42193318 | ATGAGACTCCCTCTC[-/A]AAAAAAAAAAAAAAA | 10138 |
rs745622673 | snp | A/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232357 | ACCTCATAGAAAGCT[A/T]CAACTAAAAAGATCT | 10138 |
rs745636350 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42213895 | CACAGACCTCCATTT[A/C]TAATTGGAATAAATA | 10138 |
rs745678917 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42178416 | ATCAGGATCTGCCAG[G/T]TGAAGCAAATTATTA | 10138 |
rs745698784 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42163681 | CAATTCTATGATTAT[G/T]TCATCTGGTTCAATT | 10138 |
rs745715886 | snp | C/T | 1.65121e-05 | 0.00287329 | missense, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42161704 | CTTTCTTTGACTGTG[C/T]AGGAGGCACAAACTG | 10138 |
rs745731844 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42192184 | GATAGGCAGACCAGG[A/C]CAAGAAGGGCTTTAT | 10138 |
rs745733793 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42176801 | ACCCCGTCACCACTA[A/T]AAATACAAAAAAAAA | 10138 |
rs745855424 | in-del | -/A | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234180 | CTCAAATTCTGCCTC[-/A]AAAAAAAAAAAGAGA | 10138 |
rs745948969 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42167593 | CATATTAAAACAATA[C/T]ACATATCCTGTAACT | 10138 |
rs745982584 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42185580 | TTGCTACAGCCACCC[A/C]AACCTTCAACAATCA | 10138 |
rs746025662 | snp | A/C | | | intron-variant, missense, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42199187 | GGCAGAGGCTTGAGC[A/C]AGCAGGATTGTTCCA | 10138 |
rs746118433 | snp | A/G | 1.7086e-05 | 0.00292279 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160567 | AGGACAGAAGTGACT[A/G]AGAAATTGGAGAAAA | 10138 |
rs746119148 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42164657 | ATGGTAAATTGAAGC[A/G]ATATGGTAAATCTCA | 10138 |
rs746137429 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42205932 | TTTTTTTAATTCTTG[A/G]AAATTCTTAATCATT | 10138 |
rs746141733 | in-del | -/A | | | intron-variant | YAF2 | GRCh38.p7 | 12:42189515 | GCAAGGAGAACCATT[-/A]GGGGCCTGAGAGCAT | 10138 |
rs746147084 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42198132 | AAAAAAAAAGTCATC[A/G]TGTAAGGAATCTTTC | 10138 |
rs746149095 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42214907 | TACTCAGGAGGCTAA[C/G]GCAGGAGAATCGTTT | 10138 |
rs746196697 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42193461 | TATTTATAACTTTAA[A/G]CAACCTCAGGCAGGC | 10138 |
rs746227408 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42207721 | CACGGTGAAACCCCG[C/T]CTCTACTAAAAATAC | 10138 |
rs746294402 | snp | C/T | 4.11311e-05 | 0.00453474 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42237762 | GACGCGGCGCGGGGT[C/T]ACCAGCAGGCCGCGC | 10138 |
rs746325186 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42208245 | CCTGGCTAACATGGT[A/G]AAATCCTGTCTCTAC | 10138 |
rs746362631 | snp | C/T | | | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42156814 | CTTCAGTTTTTCCTA[C/T]ATTCTTTGTTCCAGA | 10138 |
rs746426639 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42171336 | TGTAAAGTAGGTAAT[A/G]TACTATCCAGGCATA | 10138 |
rs746474717 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42192297 | AGGATCTCCTGAGCC[C/T]AGGAGATCAAGACCA | 10138 |
rs746498074 | snp | G/T | 2.93388e-05 | 0.00382996 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42237742 | GCAGGACACAACCCG[G/T]ACACGACGCGGCGCG | 10138 |
rs746499677 | snp | G/T | | | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42230955 | TAAACAACTAGGATA[G/T]TAGTTATCAGGCCTC | 10138 |
rs746516835 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42199541 | ATGAAATAGTACCAT[C/T]ACTTTTTATGCAGTA | 10138 |
rs746558476 | snp | A/G | 0.000207168 | 0.0101755 | intron-variant, synonymous-codon, missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | YAF2 | GRCh38.p7 | 12:42237610 | TCACCGGGTGGAGGT[A/G]CCCTTCCGCACATCG | 10138 |
rs746624982 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42205874 | TCAAATTTTGATACA[A/C]CACTTTTGTTGTGAT | 10138 |
rs746676383 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42221283 | CAAGGTTATAAAATG[A/G]GACTGGAGGCTAGGC | 10138 |
rs746716106 | in-del | -/AAT | | | intron-variant | YAF2 | GRCh38.p7 | 12:42168041 | TAAGTAATATTTATG[-/AAT]AATATACAAATATAT | 10138 |
rs746718893 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42169645 | CTCAAACTCCTGGAC[C/T]CAAGAGATCCACCTG | 10138 |
rs746740097 | in-del | -/AT | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157780 | ACTTTTTAAATATAC[-/AT]ATATATATATATGTA | 10138 |
rs746746408 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42216386 | ATGAAAGTAAAAGCC[A/T]TTGGAGATGGCTAAA | 10138 |
rs746819465 | in-del | -/ATGA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42218354 | TTCCCTTTTTGACTG[-/ATGA]ATATGGTTTGTCTGC | 10138 |
rs746902866 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42179576 | GGGCAAATCATTTGA[A/G]CTCAGGAGTTTGAGA | 10138 |
rs746908743 | snp | C/T | 1.76256e-05 | 0.00296859 | missense, nc-transcript-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42161637 | TTATGGCTATTCTTT[C/T]TGCTAGTTGTTTCCT | 10138 |
rs746911033 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42215072 | CTTGTTCTCCTCTGT[A/G]ACTCCATTACCTAGC | 10138 |
rs746912123 | in-del | -/AA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42230304 | AAGAAAGAAAGAAAG[-/AA]AGAAAGAAAAAGTAC | 10138 |
rs746957071 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42219423 | ACAGCTGTGTACAGA[C/T]ACTGGGAGCAGGGAT | 10138 |
rs746983325 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42178605 | AAATACAGTTTGCTC[C/T]CATTTTCATTTTTAT | 10138 |
rs747003455 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42190869 | TAACCTAAAATTTCA[C/T]TGTAGAGTATGTGGT | 10138 |
rs747049006 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42169673 | CTGCCTCAGCCTCCC[A/G]AAGTGCTGGGATTAG | 10138 |
rs747079468 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42207829 | CCAGGAGGCAGAGCT[C/T]GCAGTGAGCCGAGAT | 10138 |
rs747103472 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42224826 | TTTGTGAATAGTGCT[A/G]CAATAAACATACGTG | 10138 |
rs747111278 | in-del | -/GT | | | intron-variant | YAF2 | GRCh38.p7 | 12:42178912 | TACCCCTTTAGCCAG[-/GT]GTGGTGGTGCGTGCC | 10138 |
rs747117067 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42172859 | CATGGATGAGCCTAC[A/G]GCATTATGCTAAGTG | 10138 |
rs747166333 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42186795 | ATATTCAAACTGTTA[A/G]CATTTTAGAGGGACA | 10138 |
rs747253198 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42200523 | GGTCAATCTTTCCAG[G/T]GCTTCTTTTTGCAAA | 10138 |
rs747287021 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42185720 | TTAAATTAAGGTATA[C/T]ACATTGTTGTTTTTG | 10138 |
rs747312553 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42181694 | TCATAAAAGCAGAGA[C/T]GAAAATAATTCACAG | 10138 |
rs747351983 | in-del | -/TATT | | | intron-variant | YAF2 | GRCh38.p7 | 12:42229665 | GAACATCATAGAATG[-/TATT]TATACAAACCTAGAT | 10138 |
rs747358278 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42236204 | AAGTACTAACACAGA[C/T]ACACAAATATACTCT | 10138 |
rs747452690 | snp | C/G | 0.000162298 | 0.00900682 | intron-variant, utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42235786 | AATGTCAGGGGCCCC[C/G]ATGTGGGCCTCAAGC | 10138 |
rs747464590 | snp | A/G | 1.72323e-05 | 0.00293528 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160539 | CTTGGCATAATCTGT[A/G]TATTTGCATGGTAGG | 10138 |
rs747476621 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42195074 | CCCTTACAGTTCAGC[A/G]TGAGAAACAAGAAAC | 10138 |
rs747595490 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42158317 | CTGATATTACACTGA[A/G]AATTTAGTGAAATCT | 10138 |
rs747656335 | snp | G/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234611 | ACATGACCTACCATG[G/T]ATATAGCCAAAGGAA | 10138 |
rs747707253 | snp | A/C | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232611 | AGGAACCATGCATTT[A/C]TTTAAAAAGGACTTA | 10138 |
rs747744966 | snp | A/G | 0.000495663 | 0.0157349 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42237586 | CGGCGCGAGGGGCAG[A/G]CCCGGGACTCACCGG | 10138 |
rs747796773 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157980 | AAACATCCAAATTCT[A/T]TTTGTATGGAATTTG | 10138 |
rs747851878 | snp | A/G | | | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42156714 | CCTTCTGCTTCTGAA[A/G]AATGATCAGTAACAA | 10138 |
rs747859186 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42192465 | AGTGAGCTGTGATCG[C/T]GCCACTGCACTCTAG | 10138 |
rs747969106 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42193360 | AATTACGTATAGTCC[A/G]TAAAACTTGACAATG | 10138 |
rs748059209 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42217987 | AAAGACCATGACCAT[A/G]CTCAGACAATCCCAA | 10138 |
rs748072720 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42165701 | TGGTCTCGATCTCCT[A/G]ACCTCATGATCTGCC | 10138 |
rs748075932 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42200731 | AGATCACATTGTACA[C/T]ATCATTCTGAAATGA | 10138 |
rs748100427 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42166397 | ACCTACCTTTAGCAT[C/T]TGTCCACTAACGAAC | 10138 |
rs748108103 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42216758 | CTTCCCTCTCAAATT[A/T]TCCCCAGGCACCCCA | 10138 |
rs748125735 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42181142 | TACAGCACATTCAGA[A/G]TGGGACAAGCTGTCC | 10138 |
rs748160220 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42211628 | CATGCGCCTGTAATC[C/T]CAGCTATTAGGGAGG | 10138 |
rs748201427 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42185856 | TATTTGCTTTACTGC[A/T]ATGTTCTAGATATAG | 10138 |
rs748256105 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42160894 | TGAGCATATAATAAA[G/T]AATAAAAGTGGTAAA | 10138 |
rs748262269 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42176567 | TTCCTCTCATACTCA[C/T]ATCTAAGTCACCATC | 10138 |
rs748269027 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42209829 | TTGAGACAGAGTTTC[A/G]CTCTTGTTGCCCAGG | 10138 |
rs748307531 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42174540 | ATACCTCTTATCTAC[A/G]CTAACCCTCCAGACC | 10138 |
rs748335731 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42203353 | TTAATACAAACAGTA[C/G]TTTCATTTCTTTTAA | 10138 |
rs748389442 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42189105 | TTTCAACAGATGGAG[C/G]TGAAAAGCAGGGCAA | 10138 |
rs748443768 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42187535 | TGTTCCAAGAATACT[A/G]AAGATTGAGATACAA | 10138 |
rs748491991 | snp | C/G | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232228 | GAAGATAGCAATTTG[C/G]TGCCACTGCTTTGAT | 10138 |
rs748522199 | in-del | -/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42185456 | AAATTTTGAAAGAAG[-/T]TTTGCTGTGAGTAAA | 10138 |
rs748773852 | in-del | -/A | | | intron-variant | YAF2 | GRCh38.p7 | 12:42226488 | GCAACATAGGGAGAC[-/A]CCCCCTCTCTACCAA | 10138 |
rs748851401 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42236033 | TCTTCTAGTTTCAGT[A/C]TTTTTCTAATGGCTA | 10138 |
rs748856676 | in-del | -/ACAAATCCAGAC | | | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42161363 | ACAAAACAAAACAAA[-/ACAAATCCAGAC]ACAAATGTCTTCCAA | 10138 |
rs748862873 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42219841 | GCCTGAGATTGTACA[C/T]TTCTAACAAGCTCCC | 10138 |
rs748864585 | in-del | -/AA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42206299 | ATATGCTCTTAGTTA[-/AA]AAAAAAAAAAAAAAA | 10138 |
rs748882018 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42181197 | TAATACTTGATTTGC[C/T]CTTCACTTATCATTC | 10138 |
rs748924154 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42217055 | ACTGCCTCTTGCCTA[C/G]ACTATCAAAATGGTT | 10138 |
rs748943865 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42222583 | TGTGCTTACATAAAA[C/T]GGCAGGATTGTTAAA | 10138 |
rs748975392 | snp | C/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234966 | GCAACCCAGCCTGGG[C/T]AACAGAATGAGATCT | 10138 |
rs749110822 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42198572 | GCCTGGGCAATACAG[C/G]GAGACCCTGTTTCAA | 10138 |
rs749118765 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42190431 | ATCCTAGTTTTGCCC[C/T]TTGTTAAAAAAAGAT | 10138 |
rs749173776 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42189201 | TTTTTCAGAAAACCT[G/T]CTAGTAAATAATCAA | 10138 |
rs749175370 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42203948 | TATTCCTTCATACTT[A/G]AGATGCTGAGGAGGG | 10138 |
rs749301257 | snp | C/T | 5.77328e-05 | 0.00537244 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42161581 | ATGGTTTTATTATTT[C/T]AAAAATGTCATAAAA | 10138 |
rs749383634 | snp | C/T | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239051 | GCTTTTGAAAGAAAC[C/T]CCTATATACTCATAA | 10138 |
rs749434961 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42196677 | CCAACTAAATGGTGC[A/G]AACTGTTGCAATGAA | 10138 |
rs749438975 | snp | C/G | 1.65932e-05 | 0.00288034 | missense, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160707 | TGATCTGCAGAAGCA[C/G]CACTAGATGCAGGCG | 10138 |
rs749455739 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42163324 | CAGTCTGATTTTATC[C/T]TTAAGTGATGATAAG | 10138 |
rs749472888 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42213689 | CATGCAAATCATTCT[G/T]CTTTAACATAATTTC | 10138 |
rs749526358 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42230642 | AAAGGAAAAAGGATA[C/G]ATTTAAGAGACAATC | 10138 |
rs749628575 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42167234 | ACAGTTACAGCAAAC[C/T]ACCATGACACATGTC | 10138 |
rs749633479 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42223413 | CCAGCAATGAAGTGC[C/T]AGCTGTTTCAAAGAA | 10138 |
rs749637972 | in-del | -/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42170045 | TGGGTAATTTTTTTA[-/T]TTTTTTGTAGAGATG | 10138 |
rs749692741 | in-del | -/GGCCGCGGG/GGCCGCGGTGGCCGCGGG | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238485 | GGGGGTGGCCGCGGT[-/GGCCGCGGG/GGCCGCGGTGGCCGCGGG]GGCCGCGGCTGCCTC | 10138 |
rs749701052 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42185300 | GTTGCTTATTACAGA[C/T]AAACACACAAAGTGG | 10138 |
rs749714820 | snp | C/G | 1.7139e-05 | 0.00292732 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238106 | CGAAGCCCTGCACGA[C/G]GGCCCTGCCGCCCGC | 10138 |
rs749772572 | snp | C/T | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42240084 | CCCTGCGCATAGATG[C/T]ATATTTTAAAGGACT | 10138 |
rs749865478 | snp | C/T | 1.67944e-05 | 0.00289775 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238226 | CCGCCGCGACCGCTC[C/T]GTTTGTCAATAAGGA | 10138 |
rs749899716 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42220936 | ATACTTACTGGTATT[G/T]CTCCTGAGAAACACT | 10138 |
rs749931252 | in-del | -/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42186817 | GAGGGACAAAGCTCA[-/T]TCAAGGGTCTGAGGG | 10138 |
rs749976720 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42185121 | AGGCAAAGGCTGCAG[C/T]GGGCCAAGATCGCGC | 10138 |
rs749982143 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42183817 | TGAAAGAAGATGCCA[C/T]CTAGGACTTTCAGAG | 10138 |
rs750040860 | snp | C/T | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239826 | GACCAGCCTGGCCAA[C/T]GTGGCGAAACCCCAT | 10138 |
rs750104354 | in-del | -/GCAAACAAACAA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42185176 | GAGCCAGACTTTGTC[-/GCAAACAAACAA]ACAAACAAACAAACA | 10138 |
rs750188056 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42204337 | ATATCCATGGGTTCT[A/G]CATCCATAGATTCAA | 10138 |
rs750202078 | in-del | -/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233522 | TGACTCAGAATTTTG[-/T]TTTTTTTGAGACAAG | 10138 |
rs750208687 | snp | A/C | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234812 | AGGCAACATAGAGAT[A/C]CCCCATCTCTACAAA | 10138 |
rs750235361 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157473 | TATCCAAACCATAGC[A/G]GGAAGTTTAAAAAAG | 10138 |
rs750257280 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42207022 | ACCCAAATATCCACA[C/T]ACTTTTTTTTCTGAA | 10138 |
rs750327100 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42171835 | CAGGTGTACTGGTGC[A/G]TGCCTGTAGTCCCAG | 10138 |
rs750327898 | snp | C/T | 0.000204311 | 0.0101051 | intron-variant | YAF2 | GRCh38.p7 | 12:42212507 | AACAAAGAAAGTGTA[C/T]AGTTTTTCCTTTAAG | 10138 |
rs750381294 | in-del | -/AACT | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157328 | GCGAATCCATTCCAG[-/AACT]AACTGAGCCTCATGA | 10138 |
rs750415280 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42222695 | TATTTAGTGTCTGTT[C/T]CATAAGTTACCTATT | 10138 |
rs750428372 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42170742 | TCCCAGCTACTGGGA[G/T]TAAGGGACAGGAGGA | 10138 |
rs750478157 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42200436 | TCTGCTGCTCCACTA[C/T]ATCAGAACCAAGCCA | 10138 |
rs750501357 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42221546 | CCTGGGTGACAGAGC[A/G]AGACTCTATCTCTTT | 10138 |
rs750519390 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42195193 | CTGGCTAGATGTCCA[A/G]GTTCTCTGTAAATGA | 10138 |
rs750561372 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42197632 | TGTAACAAAGAGGTA[C/G]GCTGAGAAAAACTAG | 10138 |
rs750565603 | snp | A/G | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42235411 | TCTGTGATGCAATCA[A/G]TATCTTCTCTAGTAA | 10138 |
rs750600882 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42216189 | TATCTTCCTACCTAC[C/T]AATATTAACCTCCTT | 10138 |
rs750687110 | in-del | -/AG | 1.65523e-05 | 0.00287678 | frameshift-variant, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160666 | TCTCTCTGTGTTATC[-/AG]AGAGCTAGAGCCGCT | 10138 |
rs750694790 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42194287 | CATTCATTCACTACT[C/T]ACTCACTCACCCAGA | 10138 |
rs750761529 | snp | C/G | 4.98252e-05 | 0.004991 | intron-variant | YAF2 | GRCh38.p7 | 12:42161789 | ATGTTAAAAAGAAAG[C/G]TATTTTAAATTACAA | 10138 |
rs750799911 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42226141 | TCTCCTTGTAGCAAT[A/G]GAATATACAATATAT | 10138 |
rs750816882 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42190056 | CGTTTTATTAAGATT[A/G]TTTTTGCTGGATGTG | 10138 |
rs750918784 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42213253 | TGAGGCCTGACAATA[C/G]ACATGTGAGTTAACT | 10138 |
rs750994321 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42201734 | GTGCCACCACGCCTG[C/G]CTAATTTTTGTATTT | 10138 |
rs750998752 | in-del | -/TAAATGTATAATT | | | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42210101 | GCAAGCCCGGCCAAC[-/TAAATGTATAATT]TTTTAGAAGCAGCTA | 10138 |
rs751046385 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42224484 | CTGCATCCATCAACC[C/T]GTCATCTACATTAGG | 10138 |
rs751074376 | in-del | -/TG | | | intron-variant | YAF2 | GRCh38.p7 | 12:42183007 | TGTAAAAGTTGTCTC[-/TG]TGTCGCATTTTGGTA | 10138 |
rs751081810 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42172035 | ACTACATTTCAAACA[A/T]TAATGCTATCTGTTT | 10138 |
rs751083341 | snp | A/G | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42235248 | CTTTAGTACTTGCCA[A/G]CCTTACTCTGGAAAT | 10138 |
rs751114629 | snp | C/G | 1.69775e-05 | 0.0029135 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238138 | CAGTCCGGGCCCCGG[C/G]GCCCGGGCGCTGTTA | 10138 |
rs751155603 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42170920 | CTTTCCCCTAATATC[C/T]GCTCTAAATGTTGAA | 10138 |
rs751172998 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42223101 | ATGAGACTGGTGAAG[A/T]AGGTAGAAATCCAGT | 10138 |
rs751185068 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42166641 | AGGATATTGTCATCT[G/T]AAGACTCATGGTCTG | 10138 |
rs751314329 | in-del | -/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42223191 | ACTATCATAGTTGGG[-/T]GAAAGGTTTCTTTGC | 10138 |
rs751334588 | in-del | -/TATC | | | intron-variant | YAF2 | GRCh38.p7 | 12:42165888 | AATTCTATCTATATC[-/TATC]TATCTATCTATCTAT | 10138 |
rs751345321 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42177970 | ATTATTAATAGTTTA[C/T]CATCTGTTTTCCTCT | 10138 |
rs751379150 | snp | A/G | | | intron-variant, utr-variant-3-prime, utr-variant-5-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42235678 | CTTCAGTTTCAATCC[A/G]AATGACAATGCTTCT | 10138 |
rs751397182 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42194404 | ATCCTAACAGTTCGG[A/G]AGGCTGAGACAGGCA | 10138 |
rs751404649 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42195431 | TAAAAAGTATTACCA[A/G]AATTTAAAGAAGGAA | 10138 |
rs751421238 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42158700 | TCTTCCCACCTATGT[A/G]GAAATATGAGTATGC | 10138 |
rs751437384 | snp | C/G | 3.2128e-05 | 0.00400786 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238215 | GCCGAGAGTCGCCGC[C/G]GCGACCGCTCTGTTT | 10138 |
rs751463420 | in-del | -/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42229415 | TTATCAATAAAAAAA[-/T]TAAATTAAAAAAAAA | 10138 |
rs751491347 | snp | C/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233832 | TGATCCTTAATTTCC[C/T]AAAGTTTCTTGCATT | 10138 |
rs751611974 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42203244 | ATGTTGGGTACTATA[C/T]TGAATTTCATATAAA | 10138 |
rs751658144 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42189041 | AAATGTGTCAGGAAA[A/G]CCTTCCTGTAGAGAT | 10138 |
rs751678032 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42198006 | TCAAATAGTATCTAC[C/T]AGGAAAAAAAGTTAA | 10138 |
rs751687608 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42174555 | GCTAACCCTCCAGAC[A/C]AGTGCTACTCAAAAA | 10138 |
rs751696553 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42200883 | ATTTACTAGCTATGA[C/G]AGTGAGTAGGTTATT | 10138 |
rs751751815 | snp | C/G | 0.000162747 | 0.00901926 | intron-variant | YAF2 | GRCh38.p7 | 12:42236025 | ATATAGGCTCTTCTA[C/G]TTTCAGTATTTTTCT | 10138 |
rs751838921 | snp | C/T | 3.31175e-05 | 0.00406911 | missense, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160678 | TATCAGAGCTAGAGC[C/T]GCTTTGACTGTGTTG | 10138 |
rs751860995 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42182329 | TTAACACTATTACAT[G/T]GTAACAGGTATTTTT | 10138 |
rs751864871 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42217740 | TGGTACAGCCCTCAG[A/G]AAGGAAACAAATATA | 10138 |
rs751949379 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42212849 | TAAATGACCCATTCA[A/C]ACAGGGGTACTACAC | 10138 |
rs751961241 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42162893 | ATACAACTTAAAAAA[C/T]AGGACTGACATAGAG | 10138 |
rs752062859 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42230370 | AGGATTGGGATAAGC[A/T]GCAGGAAATGAAGCT | 10138 |
rs752098066 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42190192 | TACAAAAAATTTTAG[A/C]AATGAGCTGGGCATG | 10138 |
rs752115406 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42168938 | GCTCATACCACCCCT[C/T]CCATCATAAGAACAC | 10138 |
rs752206712 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42161897 | AATTCCTCATATGTA[A/C]GGTAATTTAAATATA | 10138 |
rs752213231 | in-del | -/AT | | | intron-variant | YAF2 | GRCh38.p7 | 12:42166310 | AACCCTTGACAACTC[-/AT]AATTTCTTGAAGAGA | 10138 |
rs752259988 | snp | C/T | 1.65499e-05 | 0.00287657 | synonymous-codon, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160652 | TGACCTGGACATTCC[C/T]CTCTCTGTGTTATCA | 10138 |
rs752277504 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42210502 | AGAAAGTTTGGGGGA[A/G]GGGATTTGGGAGATG | 10138 |
rs752330457 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42225775 | ATACTGTTTTGGTTA[C/T]TGTAGACTTGTGGTA | 10138 |
rs752357023 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42209002 | AGAACCTAGTAATAA[C/T]ACAAAATGAGTGGGA | 10138 |
rs752364452 | in-del | -/A | 0.000188661 | 0.00971057 | intron-variant, frameshift-variant, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42199146 | CTTACCAGACTGTCC[-/A]AAAAAGAGAATGACC | 10138 |
rs752393002 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42173616 | TATTATTCCAACTGT[A/T]CCTCTTTATCATACC | 10138 |
rs752445892 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42172306 | TAAAGGACAGAAGTC[A/G]TACAAAATTATAAAT | 10138 |
rs752467811 | snp | A/G | 4.21683e-05 | 0.00459155 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238131 | GCCCGCACAGTCCGG[A/G]CCCCGGGGCCCGGGC | 10138 |
rs752494433 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42183557 | AGATCAAACCAGTCA[A/C]AACATTTCATTAAAC | 10138 |
rs752558173 | snp | A/G | 2.7212e-05 | 0.00368853 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42237730 | CCGCTTCGGCCTGCA[A/G]GACACAACCCGGACA | 10138 |
rs752562706 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42221982 | AAACACTTCAAAGGT[C/T]CCTTTTAGCTCTAAA | 10138 |
rs752720075 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42224684 | TTTCCAGCTTCATCC[A/C]TGTCCCTGCAAAGGA | 10138 |
rs752755035 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42191895 | GAGTGTTCAAGACCA[C/G]CCTGGTCAACATGGT | 10138 |
rs752796478 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42204174 | ATTGGTGACATTACA[A/G]AAAAGTGTGAACCTT | 10138 |
rs752811250 | in-del | -/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42170016 | CTGGTACCACAGGCA[-/C]CGCATCACCACACCT | 10138 |
rs752889382 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42177357 | GGAAAGTCCAAGACC[A/G]AGGTCCAGTAGGGTT | 10138 |
rs752994271 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42189601 | ATATGTGACTGTGCA[C/T]AGGTACACACACATA | 10138 |
rs753036682 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42203687 | TACAATTTTCAAATA[C/T]TGAACTGTCCTAAAC | 10138 |
rs753036766 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42220364 | CCATCCCCCACACCC[A/G]GATTCTTTACATTAG | 10138 |
rs753113160 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42192421 | GGCTGAGTTGATAGG[A/T]TCACTTGAGCCTGGG | 10138 |
rs753113777 | in-del | -/AAAAAAAAAA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42175749 | TCTGTCTCAAAAAAA[-/AAAAAAAAAA]AAAAAAAAAAAAATT | 10138 |
rs753182868 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42214460 | TACTTTTTGTAGAGA[C/T]GGGGTTTTGCCACGT | 10138 |
rs753197465 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42164303 | TATAATGTAAGAAAA[C/G]GGGGAACATTTTATT | 10138 |
rs753200864 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42213534 | AATTTTTCCAACATC[A/G]CAAATTTCAATTGTC | 10138 |
rs753201157 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42167136 | ACACACCGGGGCCTG[C/T]TGGGGAGTGGGGGGA | 10138 |
rs753244312 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42179077 | GAAAGAAAAAATACA[C/T]TTGTCTGGGCTCCAC | 10138 |
rs753290498 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42184605 | ATGAACCACCACGCC[C/T]GACCCTCAAGTCTCA | 10138 |
rs753305603 | snp | A/G | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42231638 | TTTGTAAAATCATAC[A/G]TCGGTAACTAGGAAC | 10138 |
rs753364567 | snp | C/T | | | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42237633 | GCACATCGCACATCA[C/T]GCACTTGAAGGCCTC | 10138 |
rs753376417 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42195883 | ATTAACTAAACTGGT[G/T]GTGGGGAAGAGTGGA | 10138 |
rs753378096 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42182680 | CAATGAGGTCAGAAC[A/G]GTTGTAATGTTTTTT | 10138 |
rs753382569 | snp | C/T | | | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42156677 | TTTTATCACCCTCAA[C/T]GGCCAGGGAGGGCAT | 10138 |
rs753399848 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42212762 | AATTTAAGATACAAA[C/T]TGCCTTGGGTAAATG | 10138 |
rs753577244 | in-del | -/TTTTT | | | intron-variant | YAF2 | GRCh38.p7 | 12:42165774 | CTGCGCCCGGCCAGG[-/TTTTT]TTTTTTTTTTTTTTT | 10138 |
rs753594303 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42159732 | AACTATCATTAAGTT[A/G]AAGCTTTTCTAAAAT | 10138 |
rs753598383 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42230312 | AAAGAAAGAGAAAGA[A/G]AAAGTACCATATGAT | 10138 |
rs753635384 | snp | C/T | 2.32772e-05 | 0.00341146 | intron-variant, utr-variant-5-prime | YAF2 | GRCh38.p7 | 12:42237567 | TCGCCACCCCGCCGG[C/T]CGGCGGCGCGAGGGG | 10138 |
rs753636353 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42170662 | TAAAAACAAACAAAC[A/G]AACAAAAAACTATAC | 10138 |
rs753656039 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42220689 | TTCTGGGTTGACTGT[A/C]CCTAGTATGTTCTAT | 10138 |
rs753711620 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42205024 | ACCAGGTAAATAATA[C/T]GGTATGTGAATATCT | 10138 |
rs753759958 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42184906 | ATTAGGCCGGTGTGG[G/T]GGCTTACGCCTATAA | 10138 |
rs753763704 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42169437 | TCTTTTTTTTCGGAG[A/T]CATAGTCTCACTGTC | 10138 |
rs753782308 | snp | A/G | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239401 | AAGCTGCCTCCTGAC[A/G]AAGAGTGCAGATGAA | 10138 |
rs753813082 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42183742 | AAGATCTAGCTAAGA[C/G]AGTTGATAGAGGTGG | 10138 |
rs753894457 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42214640 | CCTCTTCACCCATTT[C/G]AAATAATTCCTGTTG | 10138 |
rs753922005 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42179643 | AAAATATAAAAATGA[A/G]CCAGGCGTGGTGGCA | 10138 |
rs753923326 | in-del | -/TTTT | | | intron-variant | YAF2 | GRCh38.p7 | 12:42165775 | TGCGCCCGGCCAGGT[-/TTTT]TTTTTTTTTTTTTTT | 10138 |
rs753962194 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42176601 | TGCTTTCCATCCCCA[C/T]CTTCAAAATAAGTCT | 10138 |
rs753963790 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42221426 | AAATTTTAAAATTAC[C/T]TGGGTGTGATGGAGC | 10138 |
rs754022303 | snp | A/G | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232102 | AGACAGAATATTTTT[A/G]AAAATATGAGATGTA | 10138 |
rs754045464 | snp | C/T | 0.00038956 | 0.0139509 | intron-variant | YAF2 | GRCh38.p7 | 12:42199280 | AACACTATGTACACA[C/T]GGAACAGAATTTGAC | 10138 |
rs754054539 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42192842 | CATATAGTCACACGT[C/T]GCATAACAACATTTT | 10138 |
rs754154934 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42192119 | AAGAAATTTAGTAAG[G/T]CTGGAGAATATTGAA | 10138 |
rs754158467 | snp | C/T | 0.000315159 | 0.0125491 | intron-variant, nc-transcript-variant, missense | YAF2 | GRCh38.p7 | 12:42210677 | TGATCCAGCTTTTTC[C/T]TCTCTATCAGAATAA | 10138 |
rs754187163 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42201530 | TAAAGACATTGTGTG[C/T]GTCTCCTCCTAGGTA | 10138 |
rs754313450 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42200246 | GACATTTCCTCCTTC[C/T]CCTATTTGTATTTGG | 10138 |
rs754342626 | snp | C/T | 0.00032803 | 0.0128026 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238710 | GTCTGGACAGAAGTG[C/T]CAGCCCGGGATCTCC | 10138 |
rs754366576 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42166047 | CCTCAGCCTCCCGAG[C/T]AGCTGGGATTACAAG | 10138 |
rs754423894 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157770 | AATTATATTCACTTT[C/T]TAAATATACATATAT | 10138 |
rs754468149 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42193141 | CCAACATGGTGAAAC[C/G]CTGTCTCTCCTAAAA | 10138 |
rs754470679 | snp | C/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42235310 | AATTATTTCTTCCAA[C/T]TACTGAAACTTTTGC | 10138 |
rs754580056 | in-del | -/AAAAGAAAAGAAAA | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234215 | AAAAGAAAAGAAAAG[-/AAAAGAAAAGAAAA]GAAAGAAAAGAAACT | 10138 |
rs754603572 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42204709 | AAATGTGGTATATCC[A/G]CATACGATGATGTAT | 10138 |
rs754615110 | snp | A/T | | | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42156622 | CACTTTTTTTTTCCA[A/T]CCCTGTCCTTCATTG | 10138 |
rs754635082 | snp | C/T | | | intron-variant, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42172190 | TCTTGGGAAGCTCTT[C/T]AATTAAAGTAATTTA | 10138 |
rs754671504 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42217778 | TTCAATACACTGTGT[A/G]AATATATCATCACTT | 10138 |
rs754680681 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42223151 | CCCACATTGACACCC[A/G]AGTTGTTTGAAAGAG | 10138 |
rs754692060 | snp | C/G | 0.000144791 | 0.00850733 | intron-variant, utr-variant-5-prime | YAF2 | GRCh38.p7 | 12:42237568 | CGCCACCCCGCCGGC[C/G]GGCGGCGCGAGGGGC | 10138 |
rs754916377 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42194459 | GACCAGTCTGGCCAA[C/G]ACGGTGAAAACCCGT | 10138 |
rs754942581 | snp | A/G | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234056 | GGCACCTGTAATCCC[A/G]GCTACCACAGAGGCT | 10138 |
rs754953739 | in-del | -/AC | | | intron-variant | YAF2 | GRCh38.p7 | 12:42223335 | TTAAAATACATACAC[-/AC]ACACACACACACACA | 10138 |
rs755032658 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42221631 | TCAACTACTGACCCA[A/C]GTCACAATACTTCCA | 10138 |
rs755047598 | snp | C/T | 1.89453e-05 | 0.00307771 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42161589 | ATTATTTCAAAAATG[C/T]CATAAAACACTCTTC | 10138 |
rs755050040 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42174480 | GATTCCCTTCCAGTG[C/T]CCCAAATTTCTAAAC | 10138 |
rs755084328 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42190245 | GATACTTTGGAAGTT[C/G]AGGAAGGATGATCTC | 10138 |
rs755092139 | in-del | -/A | | | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42156769 | TTATTCTGATCAGTG[-/A]TTTTTGTCATTGGTA | 10138 |
rs755172994 | snp | C/G | 0.000198708 | 0.00996568 | intron-variant | YAF2 | GRCh38.p7 | 12:42205833 | AGATTATAAATTTAT[C/G]CCCAAGTACCATTTT | 10138 |
rs755233664 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42214257 | TGCCGTTAACTACAA[C/T]TCTTTCACAAATACC | 10138 |
rs755291223 | snp | C/G | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238790 | GCCTGCAGTATACCG[C/G]GGGGAAGGCGGGAAC | 10138 |
rs755323372 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42187425 | TTGGCCTCCCAAAAT[A/G]CTGGGATTACAGCCC | 10138 |
rs755368300 | in-del | -/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42185269 | AATCTCATGACCAAG[-/C]TTTCACAGATGAGGA | 10138 |
rs755396067 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42162980 | TAATGGCTGAGGTTA[A/G]AAAAGAAAAGGGTTA | 10138 |
rs755493565 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42176471 | TTCCAATCTTCAACA[A/G]TCTTTTTATCTCTCA | 10138 |
rs755617739 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42195721 | GGCTACAGAACACTG[C/T]AGAGAATAGACCATC | 10138 |
rs755643648 | snp | A/G | 0.00016384 | 0.0090495 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238613 | GAAAACGTCTGTCCC[A/G]CCGACTGGCAGGGGA | 10138 |
rs755670919 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42194662 | ATCTAATTATGTCCT[A/G]TAATATTCTAAATCA | 10138 |
rs755696253 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42209043 | AAGCAAGAAACTATA[C/T]AGTAACATTTACAAA | 10138 |
rs755736255 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42180905 | GTAAGCTGAGATTGT[A/G]CCACTGCACTCCAGC | 10138 |
rs755794200 | in-del | -/CA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42192343 | AAGACCTCATCTCCA[-/CA]CACACACACACAAAA | 10138 |
rs755822699 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42209316 | CACCTGTAATCCCAA[C/T]ACTTAGGGAGGCCAA | 10138 |
rs755842424 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42169355 | CTCTTAGAACTTCCT[C/T]TTCCAGCCCCTTTAA | 10138 |
rs755879360 | in-del | -/ACACA | 0.000193517 | 0.00983469 | intron-variant | YAF2 | GRCh38.p7 | 12:42199275 | AAAGAAACACTATGT[-/ACACA]TGGAACAGAATTTGA | 10138 |
rs756011660 | in-del | -/AAC | | | intron-variant | YAF2 | GRCh38.p7 | 12:42226295 | CACAAATGAGATCAT[-/AAC]AATATTATACAACTT | 10138 |
rs756037924 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42167967 | TCCCAAGATTACTGG[A/G]TAAGCCAAATAAAAT | 10138 |
rs756060529 | snp | C/G | 0.0001628 | 0.00902073 | intron-variant | YAF2 | GRCh38.p7 | 12:42236031 | GCTCTTCTAGTTTCA[C/G]TATTTTTCTAATGGC | 10138 |
rs756061608 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42182532 | TACAATATCATTGGA[A/G]AAGATGAGCTGGAAT | 10138 |
rs756096987 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42224780 | CCAGTCTATCATTGA[C/T]GGGCATTTGGGTTGG | 10138 |
rs756106035 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42237300 | ACATTTTTATACCCA[A/G]AATGGGGAGAGGGGC | 10138 |
rs756143921 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42217998 | CCATGCTCAGACAAT[C/T]CCAACCTTGAAAACA | 10138 |
rs756151943 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42163108 | TTGAAGTAGAGCCCA[A/G]GAAACTGTATTTCTA | 10138 |
rs756162923 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42213559 | ATTGTCTCAAGCCAA[C/G]TTGAGTGGCTCTAAG | 10138 |
rs756189635 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42178171 | TTTTAATGAATGAAC[A/G]TTAAACCATCCTACA | 10138 |
rs756193137 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42177544 | TTAGGACTCCACTTT[C/T]ACGAGTTCATTTAAT | 10138 |
rs756245060 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42176600 | ATGCTTTCCATCCCC[A/G]CCTTCAAAATAAGTC | 10138 |
rs756253939 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42230553 | GATCATGTTAGTAGC[A/G]TTCCAAAGGAGAGAC | 10138 |
rs756298522 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42190377 | AAATGAAAAAGAATT[A/G]TTAATACTGTTTATA | 10138 |
rs756309298 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42217285 | GAAAATGGTTTTATT[C/T]CTAATTTTTAGTTCC | 10138 |
rs756311390 | snp | A/G | 3.86056e-05 | 0.00439332 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42161564 | AAGGTTAAAAAAATT[A/G]AATGGTTTTATTATT | 10138 |
rs756312056 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42191926 | GAAACCCTGTCTCTA[A/C]TAAAAATACAAAAAT | 10138 |
rs756331542 | snp | G/T | 1.65652e-05 | 0.0028779 | synonymous-codon, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160697 | TTGACTGTGTTGATC[G/T]GCAGAAGCAGCACTA | 10138 |
rs756399162 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42218975 | TAATAGCTCTTCTTT[C/T]TGAAATGTGAGGGTA | 10138 |
rs756399172 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42189793 | GTTTCATAAGTACCA[A/G]TTGATGGTGTATGCT | 10138 |
rs756403033 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42221328 | CTGTAATCTCAATAC[C/T]TTGGGAGGCTGAGGC | 10138 |
rs756413819 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42204832 | CTCCCAAAACACATG[C/T]TGTATAATTCCATTT | 10138 |
rs756445012 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42165186 | GGCCCTGCCCTCATG[C/T]GCTAAAAATTAAAAA | 10138 |
rs756468187 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42167172 | GAGGGAGAGTATTAG[C/G]ACAAATACCTAATGC | 10138 |
rs756663348 | snp | A/G | 3.64465e-05 | 0.00426871 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238147 | CCCCGGGGCCCGGGC[A/G]CTGTTACCTGGTGGG | 10138 |
rs756666032 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42219622 | CATACAACCCTGCCT[G/T]CACACACACATGCAC | 10138 |
rs756670738 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42164369 | CCTTCTGTGTGAGCA[C/G]GAGGTCAATACATGT | 10138 |
rs756671941 | snp | C/G | 3.06828e-05 | 0.00391669 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42237747 | ACACAACCCGGACAC[C/G]ACGCGGCGCGGGGTC | 10138 |
rs756685269 | snp | A/G | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239456 | CCTTCATGCACATGG[A/G]TTACTTCTGCATAAA | 10138 |
rs756691798 | snp | C/G | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238556 | CCCTTGGTACCCCCG[C/G]CTGCCGGGGACTGCC | 10138 |
rs756715099 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42183794 | CAATGTAGACAAAAA[A/G]GCATTATTGAAAGAA | 10138 |
rs756730390 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42185009 | TGGCGCAACCCTGTC[G/T]CTACCAAAAATGCAA | 10138 |
rs756784097 | in-del | -/AGAAAA | | | intron-variant, cds-indel | YAF2 | GRCh38.p7 | 12:42234218 | AGAAAAGAAAAGAAA[-/AGAAAA]GAAAAGAAAGAAAAG | 10138 |
rs756821996 | snp | C/T | | | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42156770 | TATTCTGATCAGTGA[C/T]TTTTGTCATTGGTAA | 10138 |
rs756838823 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42182695 | GGTTGTAATGTTTTT[C/T]CCACAGAAAGAAAAC | 10138 |
rs756936825 | snp | A/C | 0.000191142 | 0.00977418 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238142 | CCGGGCCCCGGGGCC[A/C]GGGCGCTGTTACCTG | 10138 |
rs756957942 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42198736 | ACTACAATTGATTAA[C/T]AGTTAAGATAAGAGC | 10138 |
rs756981223 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42230713 | AGCTGAGACAATGAC[A/G]GTTTCTAGCTGAGGT | 10138 |
rs757113145 | in-del | -/AG | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42159198 | ATATCACAACTGTTA[-/AG]GGGTCTACAGTTTTA | 10138 |
rs757231982 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42219299 | GTTTGTTACTTGATT[C/G]TAACAGGCAAACCTC | 10138 |
rs757329563 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42165213 | AAAACAAAAAAACTG[C/T]GTGTTGTGATAGAGA | 10138 |
rs757347474 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42199104 | ACATCTTCAACAAGA[C/T]GATTTTAAGGTGAAA | 10138 |
rs757373902 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42164552 | GGAAAGAAAGAAAAA[C/G]AGTATTAAAAACAAT | 10138 |
rs757495718 | snp | C/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232194 | CTGCATGCATGTACA[C/T]GGTGGTGAATATTAC | 10138 |
rs757555900 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42192964 | CACATAGTACTCATG[A/T]GTTTGCAGTGATGCT | 10138 |
rs757585643 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42224553 | CCGCGACAGGCCCCC[A/G]TGTGTGATGTTCCCC | 10138 |
rs757656683 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42186482 | GGAGTTTGAGATCAG[C/T]GTGACCAACGTGGTG | 10138 |
rs757711618 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42200318 | TTTGCATGTATCAAC[C/T]GAATCAAAATTATTT | 10138 |
rs757785431 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42205463 | TCACTGCAACCTCCA[C/T]CTCCTGTGTTCAAGC | 10138 |
rs757788249 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42185339 | TATGGAATCTACTCC[C/T]GGTGAAGATGCTGTG | 10138 |
rs757820160 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42170838 | AGATCCACCTCTCCA[A/C]TAGTATCATTATTAC | 10138 |
rs757843913 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42222840 | ATTAAATGATAAAGC[C/T]ATTATCACAGTGGCT | 10138 |
rs757968316 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42221211 | GTATAGGCAAAATTA[C/T]AAGAAGAAATCTTTA | 10138 |
rs758033816 | snp | A/G | 2.74699e-05 | 0.00370597 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42237731 | CGCTTCGGCCTGCAG[A/G]ACACAACCCGGACAC | 10138 |
rs758050949 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42201624 | GAGCCCAGGCTGGAG[A/G]GCAGTGGCACAATCT | 10138 |
rs758071965 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42184074 | ATTTAAAATATTCAG[C/T]TCACCGTTAAGACCT | 10138 |
rs758126162 | in-del | -/A | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42235536 | TCTTAGGTTTAACTT[-/A]AGAGCCAAAATCAAA | 10138 |
rs758243828 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42177689 | TGGCTTTCTACTTCT[A/G]CCCGAGGGTTTCCCC | 10138 |
rs758260221 | in-del | -/CT | | | intron-variant | YAF2 | GRCh38.p7 | 12:42212916 | GGGTCATCTAGGTAA[-/CT]CTGCTAGTTTACTAG | 10138 |
rs758261193 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42179507 | AGTTGGGAACCAGTG[A/C]CTGAAACACATCAAA | 10138 |
rs758284663 | snp | A/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232364 | AGAAAGCTTCAACTA[A/T]AAAGATCTCAGGGAC | 10138 |
rs758324942 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42176747 | TGGGTGGATCACCTG[A/C]GGTCAGAAGTTCAAG | 10138 |
rs758332145 | in-del | -/TT | | | intron-variant | YAF2 | GRCh38.p7 | 12:42165777 | CGCCCGGCCAGGTTT[-/TT]TTTTTTTTTTTTTTT | 10138 |
rs758459366 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42201772 | AGACAGGGTTTCACC[A/G]TGTTGATCAGGCTGG | 10138 |
rs758491199 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157135 | ATTTATTTTGGCTTA[-/T]GAGTCCAAAGGCTGA | 10138 |
rs758511113 | snp | C/T | 0.00038956 | 0.0139509 | intron-variant, nc-transcript-variant, missense | YAF2 | GRCh38.p7 | 12:42212477 | TTATGATTTCATGAT[C/T]CTTCATTCTATGGAA | 10138 |
rs758512472 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42200484 | ACACCAGTATCAAGA[A/G]TAAATGAAGATTAAA | 10138 |
rs758542779 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42217689 | AATATAAATGTCAAG[A/G]AGGGGATTTAAACTG | 10138 |
rs758660304 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160151 | AACCTGTTGCAGCAA[C/T]AGTTAAGTTGTTCTT | 10138 |
rs758704082 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42180863 | TGAGGCATGAGAATC[A/G]CTTGAATCCAAGAGA | 10138 |
rs758755861 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42176286 | ACCATCACGCCAGCT[A/G]ATTTTTGTATTTTAA | 10138 |
rs758775571 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42210915 | GCTATATTTTAATAT[A/C]CAAAAATATCAGCCA | 10138 |
rs758784899 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42174254 | GTCAGGCTCTTGTCC[G/T]TCCACTCCAGCAAAA | 10138 |
rs758797995 | in-del | -/A | | | intron-variant | YAF2 | GRCh38.p7 | 12:42203665 | CCTAAATTTTCTTAT[-/A]AATTGATACAATTTT | 10138 |
rs758827289 | snp | A/G | 1.65488e-05 | 0.00287647 | missense, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160659 | GACATTCCTCTCTCT[A/G]TGTTATCAGAGCTAG | 10138 |
rs758850966 | in-del | -/CA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42188681 | GTGAGCCACAGTGCC[-/CA]GTCAGAATTTTTTTT | 10138 |
rs758895055 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42226216 | AGTCAAGAAACACTT[C/T]GTTTTTAGCTATATT | 10138 |
rs758909996 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42188947 | ACTCAGAACGTAGTA[C/T]ACTTTCAAGCATTTG | 10138 |
rs759001425 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42224675 | AAATGATGGTTTCCA[A/G]CTTCATCCATGTCCC | 10138 |
rs759088783 | snp | C/T | | | intron-variant, missense | YAF2 | GRCh38.p7 | 12:42237417 | GCCTCTTCAATTACC[C/T]CTCACCGCAAACCAT | 10138 |
rs759110956 | snp | C/G | | | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42237965 | GCGGCCGCTCCGGTC[C/G]CCGCCGCCATCGCGG | 10138 |
rs759125572 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42201449 | CTTTATATCCATTGT[C/T]CATTTTATGTGTATC | 10138 |
rs759198704 | snp | G/T | 1.66233e-05 | 0.00288295 | missense, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160789 | CAGTAACTTCCAAAT[G/T]CTGAGCACTACTCCG | 10138 |
rs759277493 | in-del | -/AG | | | intron-variant | YAF2 | GRCh38.p7 | 12:42173789 | TTCTAAGTACTGGGA[-/AG]AGAGCACTGAACAAA | 10138 |
rs759286570 | snp | A/G | 1.65449e-05 | 0.00287614 | missense, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160638 | CCTCTGGGTGAAGAT[A/G]ACCTGGACATTCCTC | 10138 |
rs759337990 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42237004 | CCATTTAATCAAACT[A/G]AAGATATAAAGGTAC | 10138 |
rs759352752 | in-del | -/ATC | | | intron-variant | YAF2 | GRCh38.p7 | 12:42181206 | ATTTGCCCTTCACTT[-/ATC]ATTCTAATACAACTG | 10138 |
rs759390195 | snp | G/T | 3.41361e-05 | 0.00413121 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238125 | CCTGCCGCCCGCACA[G/T]TCCGGGCCCCGGGGC | 10138 |
rs759423352 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42195591 | AGGCTCAGAATTAAT[G/T]ATTATTAAAAGAGCT | 10138 |
rs759521559 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42185999 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGACCA | 10138 |
rs759531261 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42204514 | GAGATCATGTAATGC[A/C]TATGGGAGAATATGC | 10138 |
rs759555729 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42170032 | CGCATCACCACACCT[G/T]GGTAATTTTTTTATT | 10138 |
rs759612664 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42184606 | TGAACCACCACGCCC[A/G]ACCCTCAAGTCTCAT | 10138 |
rs759734612 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42169224 | GACTTCTGTGTATCA[C/T]GACATTATTTAACAT | 10138 |
rs759739448 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42220130 | TTTTTCCCATTCTTC[C/T]AATGAGAGATACTTC | 10138 |
rs759799904 | snp | G/T | 0.000186968 | 0.00966691 | intron-variant | YAF2 | GRCh38.p7 | 12:42210709 | AAGATTATTTCATTT[G/T]ATTTGAGATTATTAT | 10138 |
rs759859489 | snp | A/C | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239165 | CATACTAAAGGTCCT[A/C]ATACTCCAGACTCCA | 10138 |
rs759868384 | snp | A/G | 0.000162272 | 0.00900608 | intron-variant, missense, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42235873 | TCCTTCTTCTTCCAG[A/G]TGCCAGGTATTCAGC | 10138 |
rs759888468 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42177197 | AGTCTCTATGTGATA[C/T]AGGCTCTTCCTATCT | 10138 |
rs759972167 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42179062 | TCTCTCTTTCAAAAA[A/G]AAAGAAAAAATACAC | 10138 |
rs759976670 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42191797 | GTGAATAAGAATCAA[C/G]AAAGATTTGGCCATG | 10138 |
rs759985565 | snp | A/G | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42231297 | GAAGAGTGGCATCGT[A/G]TATTTTTGCAAACCT | 10138 |
rs760018587 | in-del | -/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42230297 | GAAAGAGAAGAAAGA[-/G]AAGAAAGAGAAAGAA | 10138 |
rs760051390 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42192649 | GAGAGACTAAGTAGC[A/C]CACTATTAGAGTAGC | 10138 |
rs760059485 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42218696 | CTGGCTCCCAAAATA[A/G]TCTTATTAAATGTTA | 10138 |
rs760099074 | in-del | -/CT | | | intron-variant | YAF2 | GRCh38.p7 | 12:42170637 | CAATATGGTGAAACC[-/CT]GTCTCTACTAAAAAC | 10138 |
rs760151191 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42192290 | AGGCAGGAGGATCTC[C/T]TGAGCCCAGGAGATC | 10138 |
rs760191155 | in-del | -/ACTAATA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42202243 | TTTGTCTTTTCCTGT[-/ACTAATA]ACTAATACTATACTT | 10138 |
rs760241916 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42162057 | ATTTTAAATGTATAT[A/C]AAAAAAAATGGGATG | 10138 |
rs760279200 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42225860 | TGTTTTGGGTATACA[G/T]GCTCTTTTTTGGTTC | 10138 |
rs760284460 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42230201 | GGCGGAGATTGCAGT[G/T]AGCCAAGATCGCGCT | 10138 |
rs760317748 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42215321 | AACACCTGTAATTCC[A/T]GCACTTTGGGAGGCT | 10138 |
rs760430848 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42184862 | GAGGAAGTAACAGCA[A/G]ATGTGGTAGAAATAG | 10138 |
rs760434327 | snp | C/T | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239224 | CTCCACTTCTACCTC[C/T]CCAATGTATTCAGTA | 10138 |
rs760479190 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42198370 | GGTGGATCACTTTGA[A/G]CTCAGGAGTTTGAGA | 10138 |
rs760530640 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42214186 | CACCCTCTGCCTCAC[C/T]ATGCACTAGTCTTTG | 10138 |
rs760621073 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42197009 | GCAGTGTCTGTTTTG[C/T]TCACTTCTCAGAAAG | 10138 |
rs760738946 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42206334 | TGACGTCTGGCTGGG[A/C]GCAGTGGCTCACGCC | 10138 |
rs760794588 | snp | A/C/T | 6.41977e-05 | 0.00566529 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238202 | GCTATCACCGCACGC[A/C/T]GAGAGTCGCCGCCGC | 10138 |
rs760856829 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42179244 | GGAGGCCACAGTGGC[C/T]GTATCACCTGAGGTC | 10138 |
rs760968325 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42220840 | ACACATCCAGTCATT[C/T]ACACATTCACATATT | 10138 |
rs760981497 | in-del | -/AT | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157781 | TTTTTAAATATACAT[-/AT]ATATATATATATGTA | 10138 |
rs761056288 | in-del | -/AAAT | | | intron-variant | YAF2 | GRCh38.p7 | 12:42224039 | CCAGAAGTTAAAGTA[-/AAAT]AAATAAATAAATAAA | 10138 |
rs761101631 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42200108 | ACTAAATTTTGGAGA[C/T]AAAATAGTGAAGAAG | 10138 |
rs761145080 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42179152 | CTCTTATTTGTTTAG[C/T]TGTGAAGTTTCCAAG | 10138 |
rs761150982 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42215845 | GAGAATCACTTGAAA[C/G]CAGGAGGCAGAGGTT | 10138 |
rs761195334 | snp | C/G | 0.000147612 | 0.00858978 | intron-variant, nc-transcript-variant, missense | YAF2 | GRCh38.p7 | 12:42210642 | GATTACCCAATAGGA[C/G]AACTCCAGTTACTGG | 10138 |
rs761203545 | snp | A/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233336 | TGAAACCCAAACCAA[A/T]AATTCTATCATTTTC | 10138 |
rs761215750 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42196483 | GTCCCTTTGGCTATA[C/T]CAGAAGTTTCATAAT | 10138 |
rs761291975 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42169177 | CCAAGTATGCCAAAA[C/T]CAAAAGACAGCTTTC | 10138 |
rs761357783 | snp | G/T | 0.000193314 | 0.00982973 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238218 | GAGAGTCGCCGCCGC[G/T]ACCGCTCTGTTTGTC | 10138 |
rs761358756 | snp | C/T | 0.000282805 | 0.0118879 | intron-variant, synonymous-codon, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42210586 | CGGTTCCTTGGTCCT[C/T]GAGGCACTCACAATA | 10138 |
rs761377590 | in-del | -/CA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42192342 | GCAAGACCTCATCTC[-/CA]CACACACACACAAAA | 10138 |
rs761404585 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42164804 | ACCAAGCGTGGTGGC[G/T]CACACCTGTAATCCC | 10138 |
rs761427154 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42177289 | CATAACAAAATACCA[C/T]AGACTGGGTAGCTTA | 10138 |
rs761465890 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42178939 | GTGCCTGTAGTCTTA[C/T]GTACTCAGAAGGCTG | 10138 |
rs761469350 | in-del | -/TT | | | intron-variant | YAF2 | GRCh38.p7 | 12:42209833 | GACAGAGTTTCGCTC[-/TT]GTTGCCCAGGTTGGA | 10138 |
rs761496882 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42206974 | TTTGCTTTACCTTTT[C/T]TCTCTCTCTCTCCAT | 10138 |
rs761577496 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42171741 | GGTGGATTATTTGAG[A/C]TCAGGAGTTCAAGAC | 10138 |
rs761584779 | snp | C/G | 1.65888e-05 | 0.00287996 | missense, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160602 | CTTTAATGAGATTCT[C/G]CATTCAATGATGAGG | 10138 |
rs761585192 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42212741 | TCTGTGATAGATTCT[C/T]ACTTAAATTTAAGAT | 10138 |
rs761587079 | snp | C/T | | | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42231106 | CTTAAAATTTAAGAG[C/T]TTTTGTTTTTTGTTT | 10138 |
rs761627907 | snp | A/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234277 | CAGCATCTTGAAAAT[A/T]ATGTGTCACCGTGGC | 10138 |
rs761653561 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42223973 | GATGGAGCAAACCAC[C/T]GTGGCACATGTATAT | 10138 |
rs761711593 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42204180 | GACATTACAGAAAAG[G/T]GTGAACCTTTGTACA | 10138 |
rs761790973 | snp | A/G | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42235291 | TAATAAGTCAATTAT[A/G]GAGAATTATTTCTTC | 10138 |
rs761836237 | snp | C/T | 5.76834e-05 | 0.00537014 | intron-variant, synonymous-codon, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42237697 | CCAGTAACCCTCATC[C/T]GAGGACGGCTTCGGC | 10138 |
rs761925005 | snp | A/C | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233576 | GAGTGCAGTGGTATG[A/C]TCACAGCTCACTGCA | 10138 |
rs761958080 | in-del | -/A | 0.458454 | 0.138011 | intron-variant, utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42235761 | CTTAGATGTACTGGT[-/A]AAAAAAAAAAATGTC | 10138 |
rs761997661 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42224510 | TTAGGCAATTCTTCT[A/G]ATGCTATCCCTCCTC | 10138 |
rs762062386 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42221459 | GCCTGTAGTCCTAGC[A/T]ACTTGGGAGGTTGAG | 10138 |
rs762093383 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42172993 | CTCAGGGTTAGGACA[C/T]TAAGGAACAAAATGG | 10138 |
rs762099155 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42197271 | GTTCTTCCTTTGGCT[A/G]TGAACCCTCCTCTAA | 10138 |
rs762121052 | snp | A/C | 4.5468e-05 | 0.0047678 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238115 | GCACGAGGGCCCTGC[A/C]GCCCGCACAGTCCGG | 10138 |
rs762158403 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42202661 | TCTATTTTTTGAGAT[A/G]GAGTGTCGTTCTTGT | 10138 |
rs762184937 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42171083 | CTGCAACCTCCGTCT[C/T]CTGGGTTCAAGCAAT | 10138 |
rs762209823 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42218859 | ATGTGTCTAAGAAGA[C/T]GAGTGGGGGGAAAAA | 10138 |
rs762260212 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42200352 | TTGTCTCTTTATCTG[C/T]AAAGCTGAACTCCTT | 10138 |
rs762285951 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42166067 | GGGATTACAAGCGTG[C/T]GCCACCATGCCTGGC | 10138 |
rs762301563 | snp | A/G | 0.000116053 | 0.00761661 | intron-variant | YAF2 | GRCh38.p7 | 12:42161782 | TGTGTGCATGTTAAA[A/G]AGAAAGGTATTTTAA | 10138 |
rs762346449 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42173511 | AATTTGAAAGACTAA[A/G]GACAATCTTCAAGAC | 10138 |
rs762466100 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42182007 | ATAGTGGCATGAAAC[A/T]TCAAAGTTTTTGAAT | 10138 |
rs762523652 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42201049 | ACAAGGAGTTTCTTA[A/C]GTTGAAATAAATACT | 10138 |
rs762532690 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42165878 | TCTTGGTTTTAAATT[C/T]TATCTATATCTATCT | 10138 |
rs762533300 | snp | C/T | 1.65586e-05 | 0.00287733 | intron-variant | YAF2 | GRCh38.p7 | 12:42161773 | GAGGTTTCCTGTGTG[C/T]ATGTTAAAAAGAAAG | 10138 |
rs762564691 | snp | C/T | 1.77672e-05 | 0.00298048 | intron-variant | YAF2 | GRCh38.p7 | 12:42160854 | AAATGAAATTTTAAA[C/T]TAGCTTTTCCCTCTA | 10138 |
rs762586054 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42191659 | CTATGTGCCAAGCAT[C/T]ACACTTAGTGTTAGG | 10138 |
rs762647191 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42194302 | CACTCACTCACCCAG[A/G]GCAACCTCCAGCCTT | 10138 |
rs762673890 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42158655 | ATCTCCATGCTACAC[C/T]GTGTTCCCGTCTATG | 10138 |
rs762678828 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42236850 | AAGAATGCCACTGAC[G/T]GAATTTCCTGGATGA | 10138 |
rs762704472 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42208952 | AGCAGGACACCACTA[C/T]GAGCTCTTTATATTT | 10138 |
rs762728986 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42173168 | CACAGTCATAGACAC[G/T]GCAGCCTCAAACTCC | 10138 |
rs762768516 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42206536 | ATCGCTTGAACCCAG[C/G]GGGTGGAGGTTGAAG | 10138 |
rs762768647 | snp | A/C | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42240022 | GCCTCTAAGTAAATA[A/C]ATAAATAACATTTTT | 10138 |
rs762778857 | snp | C/T | 4.21647e-05 | 0.00459136 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238132 | CCCGCACAGTCCGGG[C/T]CCCGGGGCCCGGGCG | 10138 |
rs762785202 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42225504 | TTCCAGGGATTTTAT[C/G]GTTTTAGGTCTTATG | 10138 |
rs762889816 | snp | A/C/G | 0.000191331 | 0.0097793 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238205 | ATCACCGCACGCCGA[A/C/G]AGTCGCCGCCGCGAC | 10138 |
rs762908043 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42224371 | ATTTAGGTGAAGAAT[A/T]CAATATATTTCTTTT | 10138 |
rs762915082 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42219208 | GCCAATTCCATGAAA[A/C]CTTAGGAATCCACTC | 10138 |
rs762927572 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42219021 | ATTAACCTAGCCTGT[A/G]CTGAACAGAATTTGA | 10138 |
rs762927990 | in-del | -/A | | | intron-variant | YAF2 | GRCh38.p7 | 12:42182591 | TATAGAAGAGGTTGC[-/A]AAAGATTGCCTAATC | 10138 |
rs762936764 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42208336 | GAGGCTGAGGCAAGG[G/T]AATTGCTTGAACCTG | 10138 |
rs762973144 | in-del | -/TT | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42231659 | ACTAGGAACCATTTG[-/TT]TTTGCTGAGTTATGC | 10138 |
rs762993704 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42236633 | TGAATATTTGTATAT[C/G]TCAATATTACATGTG | 10138 |
rs763000900 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42171918 | GCAGTAAGCCATGAC[C/G]GTTCCACTGCACTCC | 10138 |
rs763084414 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42158232 | TAATTCATTTCTCCA[A/G]TCTCATAGTGCACAC | 10138 |
rs763107338 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42167515 | TCTATAGGTAGAACC[A/C]CTTGAAAAAGGACTC | 10138 |
rs763107485 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42183085 | TGATTGGTGATCTTT[A/G]ATGTTACTGCTGTCA | 10138 |
rs763144846 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42200419 | CTAGCACCTAGTGCT[A/T]ATCTGCTGCTCCACT | 10138 |
rs763175867 | in-del | -/TCTG | | | intron-variant | YAF2 | GRCh38.p7 | 12:42221900 | CTGAAGACGCTCTTA[-/TCTG]TCTATCATTAAGGTT | 10138 |
rs763223031 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42182274 | AACATATGATGTGGC[C/T]GGGTATTTTATAATG | 10138 |
rs763262003 | snp | C/T | 1.66186e-05 | 0.00288254 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42237659 | GCCTCGGCGCTGTTC[C/T]GGAAGGTGCAGACGC | 10138 |
rs763269693 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42191472 | GTTTCTAAACACTAA[A/G]TGCATAGGTGGGCTT | 10138 |
rs763274735 | snp | C/T | | | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42161303 | ATTATCTGTTCGGTA[C/T]GTTGAAAACCACTCC | 10138 |
rs763282136 | snp | C/G | 0.000162272 | 0.00900608 | intron-variant, missense, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42235962 | CCAAGACTGGCTGTG[C/G]AGTAGGACACCAGCT | 10138 |
rs763312315 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42202531 | TACGTAATCCTTGTG[C/T]CTCACTAATTTCATT | 10138 |
rs763395386 | in-del | -/A | 1.72372e-05 | 0.0029357 | intron-variant | YAF2 | GRCh38.p7 | 12:42160834 | TCTTGGCCTAAACAT[-/A]AAAAAAATGAAATTT | 10138 |
rs763454627 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42202753 | AAGCAATTCTCCCAC[C/T]TCAGCCTCCCAAGTA | 10138 |
rs763470320 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42197074 | GTGATGAGCTTAAAA[A/G]GGGAATTTTTTCGAA | 10138 |
rs763520847 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42219912 | TAGCAACATCCTACA[C/T]AACAACACATCTCCA | 10138 |
rs763523356 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42212645 | AAATGTAATTCTAAT[G/T]AAAATCTTTTATTTC | 10138 |
rs763541805 | snp | C/T | 1.82151e-05 | 0.00301782 | intron-variant | YAF2 | GRCh38.p7 | 12:42160867 | AACTAGCTTTTCCCT[C/T]TACCAAATTTCTGAG | 10138 |
rs763593721 | in-del | -/C | 5.64637e-05 | 0.00531306 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42237738 | GCCTGCAGGACACAA[-/C]CCGGACACGACGCGG | 10138 |
rs763618056 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42168768 | GATCTAAGGGCATAT[C/T]TGCACATTTACATGT | 10138 |
rs763665447 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42186495 | AGCGTGACCAACGTG[A/G]TGAAACCCCGTCTCT | 10138 |
rs763712997 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42209618 | AATATAAAACTATCC[C/T]TGCTGGTCAGTACTA | 10138 |
rs763738677 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42162195 | TATCTGTTCTTTAAA[A/G]CTTTTCATTTATTCA | 10138 |
rs763761517 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42222470 | TTAATTATTTGACTA[A/G]CGGACCATCTTCCTC | 10138 |
rs763762957 | in-del | -/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42175048 | TCAAAGAAGGAAATA[-/T]TATGTCCATACAAAA | 10138 |
rs763774168 | snp | A/G | | | intron-variant, missense, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42210608 | CTCACAATAACTTCA[A/G]ACAATGTGGATCTGT | 10138 |
rs763800897 | in-del | -/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42184587 | AGTGCCGGGATTACA[-/G]GCATGAACCACCACG | 10138 |
rs763820010 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42170251 | CTCCTGAAGGATTGT[C/G]TCTTTTCATTTTTGA | 10138 |
rs763906011 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42188355 | GTCCTTAGCTATATG[C/T]TCTGAACTTTGAAAT | 10138 |
rs763909684 | snp | C/T | 4.10922e-05 | 0.0045326 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238133 | CCGCACAGTCCGGGC[C/T]CCGGGGCCCGGGCGC | 10138 |
rs763942664 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42184877 | GATGTGGTAGAAATA[C/G]CAAGAGAACTAGAAT | 10138 |
rs763976642 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42237392 | TCTCTTGGCAGCAAA[A/C]AACGTTACAGCCTCT | 10138 |
rs763995817 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42183741 | GAAGATCTAGCTAAG[A/G]GAGTTGATAGAGGTG | 10138 |
rs764022607 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42230140 | CACACGTCTGTAATC[C/T]CAGCTACTCAGGAGG | 10138 |
rs764069539 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42198409 | AGCAACATGGTGAAA[C/T]TCTGTCTCTACAAAA | 10138 |
rs764075979 | snp | A/G | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239308 | TAAAGAACCACTAAC[A/G]ACTTGCCCACACTCC | 10138 |
rs764153949 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42201470 | TATGTGTATCATCTT[A/C]TTCTTTTGATCTTTA | 10138 |
rs764165653 | snp | G/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42231936 | CCAAGTCTGAATAAC[G/T]ATGGTATTTCAGGTA | 10138 |
rs764202897 | snp | C/T | 0.000162324 | 0.00900755 | intron-variant, missense, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42235992 | TTCCCCCCTTCCTTG[C/T]TGTCCCTGCAAATAA | 10138 |
rs764229363 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42219077 | CAAAAATGTTTTGCA[A/C]AACACCCTTATAAAA | 10138 |
rs764338744 | in-del | -/CT | | | intron-variant | YAF2 | GRCh38.p7 | 12:42166731 | GCTTTACACCATCCC[-/CT]GATTCATCTAGTAAC | 10138 |
rs764389200 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42192080 | ATTAGATTTAAATAA[A/T]ACAAAAAGTGTTATA | 10138 |
rs764391338 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42206868 | CACTTTCTCCTCATC[G/T]TTTTTTAAAATTTCA | 10138 |
rs764406509 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42166044 | CTACCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 10138 |
rs764424846 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42200225 | GCTTCCCGTGCTCCA[A/G]ATCAAGACATTTCCT | 10138 |
rs764464792 | snp | C/T | 2.95652e-05 | 0.0038447 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42237689 | CTACAGTCCCAGTAA[C/T]CCTCATCCGAGGACG | 10138 |
rs764478482 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42194461 | CCAGTCTGGCCAACA[C/T]GGTGAAAACCCGTCT | 10138 |
rs764480317 | snp | A/C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42215879 | GTGAGCCCAGATTGC[A/C/G]CCACTGCACTCCAGC | 10138 |
rs764667495 | in-del | -/AC | | | intron-variant | YAF2 | GRCh38.p7 | 12:42170673 | AACAAACAAAAAACT[-/AC]ATACACACACACACA | 10138 |
rs764692985 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42164991 | GCCCAGGAGGTGGAG[C/G]TTGCAGTGAGCCACG | 10138 |
rs764708247 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42198710 | TTCCGAAATGGAGAG[C/T]GGGGTTTCAGACTAC | 10138 |
rs764753800 | snp | A/G | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239513 | TCTGTCCATCTTTCT[A/G]GGTTTACATCAAGTC | 10138 |
rs764783779 | snp | C/T | 1.65496e-05 | 0.00287655 | missense, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160651 | ATGACCTGGACATTC[C/T]TCTCTCTGTGTTATC | 10138 |
rs764879598 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42186765 | GTATTAAATTTGCCA[A/G]TGCCTCAATTTGGAA | 10138 |
rs764896619 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42208700 | AATATACTAGCATAA[A/T]AGGACTGATAAAAGG | 10138 |
rs764951262 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42214420 | GGGAAACCAGGCTCA[C/T]GCTACCATGCCCGGC | 10138 |
rs764951769 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42224011 | ACAAATCTTCAAGTT[C/T]TGCACATGTATCCCA | 10138 |
rs764975374 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42163928 | TATTTGATGAGAAAA[A/T]TCAGGATAGGAGGAA | 10138 |
rs765006726 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157308 | ATTCATCCATTCCTG[A/C]AAGAGCGAATCCATT | 10138 |
rs765068353 | snp | C/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234465 | CCCACCACTCTGCAA[C/T]ATACCCAAGTAACAA | 10138 |
rs765084064 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42193031 | AAGTATAGCACCTAC[C/T]GGCCGGGCACGGTGG | 10138 |
rs765184724 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42170685 | AACTATACACACACA[A/C]ACACACACAAATTAG | 10138 |
rs765189703 | in-del | -/TT | | | intron-variant | YAF2 | GRCh38.p7 | 12:42174520 | CCTCAGGACTGAGTC[-/TT]TGGATACCTCTTATC | 10138 |
rs765212581 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42204268 | CAAAAGTTTAAACAC[A/G]AAGTATCACACGACC | 10138 |
rs765217498 | snp | C/T | 4.29489e-05 | 0.00463385 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238128 | GCCGCCCGCACAGTC[C/T]GGGCCCCGGGGCCCG | 10138 |
rs765249946 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42217489 | AAAGCAGTTTAAAGC[A/C]GCAACAGAATCAGAT | 10138 |
rs765306209 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42166106 | TATATTTTTAGGGGG[A/T]TTCACCATGTTGGCC | 10138 |
rs765350859 | in-del | -/AACAC | | | intron-variant | YAF2 | GRCh38.p7 | 12:42218185 | ATCAGGCTACTAGGA[-/AACAC]ACACACACACACACA | 10138 |
rs765373157 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42195159 | ATGGATAAAGAAATC[G/T]AGAGAGAGAGAAAAA | 10138 |
rs765375940 | snp | C/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42235368 | ATCTTGTTTTTTTAA[C/T]ATTACCAGAGAGGAA | 10138 |
rs765377380 | snp | A/C | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233583 | GTGGTATGATCACAG[A/C]TCACTGCAACCTCGA | 10138 |
rs765437682 | snp | C/T | 0.000216802 | 0.0104093 | intron-variant | YAF2 | GRCh38.p7 | 12:42212408 | AGATACAGATATATT[C/T]TAATACCCTTTACCA | 10138 |
rs765477077 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42180687 | GCACAGGTGGCTCAC[A/G]CCTGTAATCTCAGCA | 10138 |
rs765508587 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42197396 | CAGTGGATGGGAGAA[G/T]AAGAAGAATATTCTT | 10138 |
rs765534064 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42194270 | TCCTAGGCCTTCCTT[C/T]ACATTCATTCACTAC | 10138 |
rs765570169 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42189951 | AATAGCAAAAGCAGC[C/T]ACGTTTAATTCTGAA | 10138 |
rs765644953 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42202669 | TTGAGATGGAGTGTC[A/G]TTCTTGTCTCCCAGG | 10138 |
rs765651878 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42225910 | TTTTTCTAATTCTGT[A/G]AAGAAAGTCAATGGT | 10138 |
rs765669026 | in-del | -/A | | | intron-variant | YAF2 | GRCh38.p7 | 12:42209258 | TTAAGAAGTGCTAGG[-/A]AAAAAAAAAAAAAGT | 10138 |
rs765727694 | in-del | -/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42188384 | ATATATATATTTTGC[-/T]TTTTTTTTTTTTTTT | 10138 |
rs765745026 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42171933 | CGTTCCACTGCACTC[C/T]AGAATGGGAGACAGA | 10138 |
rs765805791 | in-del | -/TAAACT | 1.68105e-05 | 0.00289914 | cds-indel, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160583 | AGAAATTGGAGAAAA[-/TAAACT]TTAATGAGATTCTCC | 10138 |
rs765865859 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42212981 | AGGTCTTATATGTTT[A/G]TAGTGATAAAACAGA | 10138 |
rs765933201 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42187672 | CTGAGGAGTAAAATA[C/T]ATATAGCATGAAAAT | 10138 |
rs765954890 | in-del | -/AAAAGAAAAGAAA | 0.00451465 | 0.0472963 | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234195 | CAAAAAAAAAAAGAG[-/AAAAGAAAAGAAA]AGAAAAGAAAAGAAA | 10138 |
rs766024634 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42195376 | CTTCAATTTAAAGTA[A/T]CATACAGGAAACAAA | 10138 |
rs766028157 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42191830 | CAGTGGCTCATGCCT[A/G]TAATCCCAGCAGTTT | 10138 |
rs766042214 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42237264 | CCTTGATCCCCACAC[A/T]CTAACACAACAATGC | 10138 |
rs766058855 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42186107 | GAGGCAAGAGAATTG[C/T]TTGAACCCAGGAGGC | 10138 |
rs766111964 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42185167 | TGGGCAACAGAGCCA[C/G]ACTTTGTCGCAAACA | 10138 |
rs766120236 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42166353 | TCTGCTTCAGAATTA[C/T]CATTTTCATTTGTAG | 10138 |
rs766201993 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42206674 | ACTGTTCTTTGAAAA[A/G]TTCTCCATTATAAAT | 10138 |
rs766241712 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42182874 | TGAAAATCTTGAATA[A/G]CATGAACACAAGAGC | 10138 |
rs766266945 | in-del | -/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42163871 | CTATTAAAAATAAAG[-/C]CCTTCTATCTCCAGG | 10138 |
rs766274157 | snp | C/T | 4.761e-05 | 0.0048788 | intron-variant, utr-variant-5-prime | YAF2 | GRCh38.p7 | 12:42237564 | TGGTCGCCACCCCGC[C/T]GGCCGGCGGCGCGAG | 10138 |
rs766324496 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42179820 | AAAAAGAAATCAGTA[A/G]TATTAAAAGATGTTA | 10138 |
rs766421144 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42197792 | GAGGATTTGAAATAA[A/G]TTATAGAAAATTTGG | 10138 |
rs766440898 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42202768 | CTCAGCCTCCCAAGT[A/G]GCTGGGATTACAGGC | 10138 |
rs766505417 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42217728 | TAATGGGACCAATGG[C/T]ACAGCCCTCAGGAAG | 10138 |
rs766521856 | in-del | -/AAAAG | | | intron-variant | YAF2 | GRCh38.p7 | 12:42171516 | CTTTAAATTAAAAAA[-/AAAAG]AAAGAAAGAAAGAAA | 10138 |
rs766536357 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42182275 | ACATATGATGTGGCC[A/G]GGTATTTTATAATGC | 10138 |
rs766551473 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42169002 | AGTCTCTCCCATCTA[A/G]AAGGAAAAAACTCCT | 10138 |
rs766616146 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42176828 | AAAATGTAGCTAGGC[A/G]TGGTGCTGGGCGTCT | 10138 |
rs766656725 | in-del | -/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42174100 | TTCATACCTCAAAAA[-/G]AAAAAAAAAAAAAAA | 10138 |
rs766668547 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42177293 | ACAAAATACCATAGA[C/G]TGGGTAGCTTAAACA | 10138 |
rs766710762 | snp | A/C | 0.000148181 | 0.00860631 | intron-variant, nc-transcript-variant, missense | YAF2 | GRCh38.p7 | 12:42210647 | CCCAATAGGAGAACT[A/C]CAGTTACTGGTAAGT | 10138 |
rs766714767 | snp | C/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42231253 | TATTTTAAAAACTTA[C/T]TATTTTCCAAAACAA | 10138 |
rs766750020 | snp | C/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42235602 | GAGAGGGTCGTGGTG[C/T]AGAACACTTACTTTC | 10138 |
rs766793232 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42176315 | AAATAGAGATGGGGT[C/T]TCACCATGCTGGCCA | 10138 |
rs766793266 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42191569 | CAAGCATGTTTGGTC[C/T]TGTTTTCATGTTTTC | 10138 |
rs766826527 | in-del | -/A | 1.75336e-05 | 0.00296082 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42237765 | CGGCGCGGGGTCACC[-/A]AGCAGGCCGCGCCCG | 10138 |
rs766846633 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42190168 | GGCAACACAGCAAGA[C/T]CACATCTCTACAAAA | 10138 |
rs766859544 | in-del | -/CTGG | | | intron-variant | YAF2 | GRCh38.p7 | 12:42213130 | GGCCTTTCTCTCACT[-/CTGG]GTCCAGATATCTTGC | 10138 |
rs766916721 | in-del | -/A | 1.72372e-05 | 0.0029357 | intron-variant | YAF2 | GRCh38.p7 | 12:42160835 | TCTTGGCCTAAACAT[-/A]AAAAAATGAAATTTT | 10138 |
rs766975224 | snp | C/T | | | intron-variant, nc-transcript-variant, missense | YAF2 | GRCh38.p7 | 12:42210449 | CCTGATGGGCATCCA[C/T]TGGAACTGAGGGGGC | 10138 |
rs767007322 | in-del | -/AAACA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42192509 | GTGAGACCCTGTCTC[-/AAACA]AAACAAAACAAAACA | 10138 |
rs767015207 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42168692 | AGAACACTCCATTCA[C/G]AGGAACAAGCCACTG | 10138 |
rs767016786 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42189090 | AGAGTGTGTGTAGAA[C/T]TTCAACAGATGGAGC | 10138 |
rs767028673 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42209186 | GACTTGCAACATATC[A/C]TATATTATTTTTCAA | 10138 |
rs767160919 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42183500 | AAGGAAGCAAAACAG[A/C]CTTACTACTGGGATA | 10138 |
rs767175920 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42173567 | CCTTCCTCTTAGCCA[A/G]CTAAACATTTAAGCC | 10138 |
rs767221630 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42187983 | GAAGAAAATGTTCCA[A/G]CTGAGTCAAGCCTTC | 10138 |
rs767282732 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42167770 | CAGCACTTTGGGAGG[A/C]CAACGCGGGCAGACT | 10138 |
rs767372428 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42219250 | AAACCACTGGGCCTC[C/T]TGAGGGACAGCCAGG | 10138 |
rs767380301 | snp | C/G | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239176 | TCCTCATACTCCAGA[C/G]TCCAGCAACAGCCAT | 10138 |
rs767415882 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42182461 | GTTTTATCACTTACA[A/T]CAAAACTGAAAGAAA | 10138 |
rs767424802 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42195652 | TTTACAATGTACCTA[A/T]TTTATGATGGGCATT | 10138 |
rs767433525 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42237291 | ATGCAGCCAACATTT[G/T]TATACCCAGAATGGG | 10138 |
rs767571089 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42191814 | AAGATTTGGCCATGC[A/T]CAGTGGCTCATGCCT | 10138 |
rs767595113 | snp | C/G | | | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42161493 | AAACCTTTCCTGATA[C/G]CTTATAATAAAGGAG | 10138 |
rs767663261 | snp | A/G | 2.86143e-05 | 0.00378237 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42237698 | CAGTAACCCTCATCC[A/G]AGGACGGCTTCGGCT | 10138 |
rs767685319 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42170074 | TGAGGGTCTCACAAC[A/G]TGGCCCAGGCTAGTC | 10138 |
rs767786053 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42214435 | TGCTACCATGCCCGG[A/C]TAATTTTTATACTTT | 10138 |
rs767800880 | snp | C/T | 1.83812e-05 | 0.00303154 | intron-variant | YAF2 | GRCh38.p7 | 12:42160871 | AGCTTTTCCCTCTAC[C/T]AAATTTCTGAGCATA | 10138 |
rs767819749 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42220139 | TTCTTCCAATGAGAG[A/G]TACTTCAAGTTTCAA | 10138 |
rs767905436 | snp | C/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42231448 | TTGAAAAGAGGTAAG[C/T]AGTTGAATAGCATTT | 10138 |
rs767921942 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42218721 | ATGTTATCATAATGT[A/G]TACTTTGATAGCATT | 10138 |
rs767923707 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42166974 | TTTCTGTTTTCTTAT[A/T]ATTTTGGTCTCTTTT | 10138 |
rs767932093 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42192650 | AGAGACTAAGTAGCA[C/G]ACTATTAGAGTAGCC | 10138 |
rs767951255 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42198756 | AAGATAAGAGCCCAC[A/G]AACAAGTGAAGCAAT | 10138 |
rs767992835 | in-del | -/TTCCCTC | | | intron-variant | YAF2 | GRCh38.p7 | 12:42216608 | ATGGTAGGCAATCTA[-/TTCCCTC]CCTGATCTGTCTTAC | 10138 |
rs768011924 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42220624 | TGCACCAAGAGCTTT[A/C]CCTGTTGAGCAGCTA | 10138 |
rs768089164 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42177142 | GGCAACCAGAGTATA[C/T]GGCAATCAACAAAAT | 10138 |
rs768103097 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42229034 | GTGTAGAAAGAAGTA[C/G]ACATGGGAGACTTTT | 10138 |
rs768105872 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42173297 | AACACTTCTGCAGCA[A/G]ACCAGAACACAATTT | 10138 |
rs768105931 | in-del | -/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42202104 | GCAGAGATCTAGTTT[-/C]CCCCCCCCATCTAGA | 10138 |
rs768117525 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42230514 | GACCAACATAATCAC[A/T]TAGGTTTCAAAAAAG | 10138 |
rs768153992 | snp | G/T | 1.65669e-05 | 0.00287805 | intron-variant | YAF2 | GRCh38.p7 | 12:42161776 | GTTTCCTGTGTGCAT[G/T]TTAAAAAGAAAGGTA | 10138 |
rs768237674 | snp | G/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232498 | TGAGTCCTCTTACAG[G/T]ACAAAAAACAAACAA | 10138 |
rs768244618 | in-del | -/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42217265 | GGGTATAATTTTTTT[-/T]ATAAGAAAATGGTTT | 10138 |
rs768248349 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42192383 | GCATGGTGGCACACA[C/T]CTGTGAACCCACCTA | 10138 |
rs768257019 | snp | C/T | 0.000561167 | 0.0167412 | intron-variant | YAF2 | GRCh38.p7 | 12:42210494 | TATATGTAAGAAAGT[C/T]TGGGGGAGGGGATTT | 10138 |
rs768290739 | snp | A/G | | | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42230976 | ATCAGGCCTCACACT[A/G]TAAAGGAAATAAAAA | 10138 |
rs768402001 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42199585 | CAAAAGGCACTGGAA[C/T]TCTCACATTATAAAC | 10138 |
rs768436291 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42200581 | AGTATTTTAAAAGCT[A/G]TACAGCAATATACAT | 10138 |
rs768452843 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42215080 | CCTCTGTAACTCCAT[C/T]ACCTAGCCCAGCACC | 10138 |
rs768474393 | in-del | -/A | | | intron-variant | YAF2 | GRCh38.p7 | 12:42179789 | CCCTGTCTAAAAGGC[-/A]AAAAAAAAAAAAAAA | 10138 |
rs768529163 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42218053 | CAGTAAAAAATTCTG[C/T]TTTTACTGGCTTAAT | 10138 |
rs768644003 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42165976 | AGGCTGGAGTGCGGT[A/G]GCGTGATCTTGGCTC | 10138 |
rs768670041 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42165564 | TGCCTCCTGGGTTCA[C/T]GCCATTCTCCTGCCT | 10138 |
rs768671914 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42224882 | TTTATAATCCTTTGG[A/G]TATATACCCAGTAAT | 10138 |
rs768684407 | in-del | -/TAATG | | | intron-variant | YAF2 | GRCh38.p7 | 12:42191499 | GCTTTGTATTTAATC[-/TAATG]TAAATCTTGCTTAAT | 10138 |
rs768740896 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42208104 | AAAATAAAATAATAA[A/T]TTTTTTAAAAAGAGC | 10138 |
rs768775199 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42172910 | ACCACATATTCTTGC[A/G]TGGTTCTGTTTATAT | 10138 |
rs768825290 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42185808 | TATATGAACTAGGAA[A/G]CCAAAAACTTCGTAT | 10138 |
rs768886457 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42182802 | AGAAAGCATCCTAAA[A/T]GATCATATATAATTT | 10138 |
rs768888039 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42223902 | CAAGGGGAAGGAGAG[A/C]ATTAGGACAAATACC | 10138 |
rs768899741 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42171547 | GAAATATGTTACTTG[C/T]AGAATTACTTTTAAA | 10138 |
rs768900081 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42182722 | AAACATTATTGAATA[G/T]ATTGAATTTTCCATC | 10138 |
rs768913306 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42208586 | CACTAGCCAATAAGG[A/G]TATTAACTGGGTGCT | 10138 |
rs768946642 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42218536 | TGTCTTTTAAAAAAT[G/T]TATTATTTTTTCCAG | 10138 |
rs768966525 | snp | G/T | 4.62931e-05 | 0.00481086 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238107 | GAAGCCCTGCACGAG[G/T]GCCCTGCCGCCCGCA | 10138 |
rs769053610 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42167326 | ATAAATAAAATAGTT[C/G]CTAGGATGTAATAGC | 10138 |
rs769071483 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42236278 | TCAAAATACTTAAAT[C/T]ACAAATCACGGGTCC | 10138 |
rs769091113 | snp | C/T | 3.24165e-05 | 0.00402582 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238166 | TTACCTGGTGGGGCT[C/T]TTCTTGTCTCCCATG | 10138 |
rs769223015 | snp | A/G | 6.65126e-05 | 0.00576644 | missense, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160722 | GCACTAGATGCAGGC[A/G]GTGACTTTGTTTTCT | 10138 |
rs769245228 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42178312 | CAATTGAATAAAAGA[C/T]CTCCAGGAATGAAGC | 10138 |
rs769258739 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42161156 | AAATAGTTGCACCAT[A/G]GAGGAAGGTGATAAA | 10138 |
rs769299221 | snp | A/C | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232640 | TATGTAGATGGTCCT[A/C]AATTTTTTTCTCCCA | 10138 |
rs769301151 | in-del | -/A | | | intron-variant | YAF2 | GRCh38.p7 | 12:42215071 | CTTGTTCTCCTCTGT[-/A]AACTCCATTACCTAG | 10138 |
rs769359201 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42199706 | ATAACAGTTTCACAA[C/G]CTAGCACTAACCAAA | 10138 |
rs769361170 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42216767 | CAAATTTTCCCCAGG[A/C]ACCCCAAATTCAACA | 10138 |
rs769403273 | snp | A/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234792 | CAAGAGTTTGAGACT[A/T]GCCTAGGCAACATAG | 10138 |
rs769420260 | in-del | -/TTTA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42187135 | TTACTATTTTATATT[-/TTTA]TTTATTTATTATTCT | 10138 |
rs769436808 | in-del | -/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42222937 | ATTGCTGCCAAATTC[-/T]TTTTTTTTTTTTTTG | 10138 |
rs769471838 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42178986 | TGAGGCCAGGAGTTT[C/G]AGGTTATAATGAGCT | 10138 |
rs769539177 | snp | A/G | 1.65081e-05 | 0.00287293 | missense, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42161707 | TCTTTGACTGTGTAG[A/G]AGGCACAAACTGCTG | 10138 |
rs769556023 | in-del | -/AG | | | intron-variant | YAF2 | GRCh38.p7 | 12:42218183 | CATCAGGCTACTAGG[-/AG]AAACACACACACACA | 10138 |
rs769584434 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42219654 | CACAAAAATGTGAGG[A/G]AAAAGCTCTTTGGAA | 10138 |
rs769590933 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42225400 | TTTGGCTTTTGTTGC[C/T]ACTGCTTTTGGTGTT | 10138 |
rs769619928 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42189120 | CTGAAAAGCAGGGCA[A/G]TTAAGGTAGAGAGAG | 10138 |
rs769630995 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42166502 | GCTCCAAGTTCTTTT[C/T]GCAAAATATTGCATG | 10138 |
rs769661984 | snp | C/T | 0.000140105 | 0.00836857 | intron-variant, nc-transcript-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42210406 | ACAGATCCACCTCTC[C/T]TGCCCTTCTGTTCAG | 10138 |
rs769719995 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42236687 | AGATTAGTATGCTTA[C/T]TGTTATAGTTTAGTT | 10138 |
rs769813724 | snp | A/G | 1.69312e-05 | 0.00290952 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160576 | GTGACTAAGAAATTG[A/G]AGAAAATAAACTTTA | 10138 |
rs769829669 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42212049 | CAAAAAAAAAAAAGT[A/C]TTTAACCATTTGTCA | 10138 |
rs769871774 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42200927 | TTCAGTATTCCCATA[C/T]GCAAAATGAAGATAA | 10138 |
rs769930117 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42226808 | ATAGTCAAATTTGAA[A/G]AAACATTAATTGAAA | 10138 |
rs769993656 | snp | G/T | 1.66416e-05 | 0.00288453 | intron-variant, synonymous-codon, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42237649 | GCACTTGAAGGCCTC[G/T]GCGCTGTTCCGGAAG | 10138 |
rs770058246 | in-del | -/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42190943 | TAATACAATGTAACC[-/T]ACTTAACAATGTTTA | 10138 |
rs770096596 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42200355 | TCTCTTTATCTGTAA[A/G]GCTGAACTCCTTAAA | 10138 |
rs770143330 | in-del | -/A | 0.458454 | 0.138011 | intron-variant, utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42235760 | CTTAGATGTACTGGT[-/A]AAAAAAAAAAAATGT | 10138 |
rs770200321 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42219852 | TACATTTCTAACAAG[C/T]TCCCAGGTGATGCTA | 10138 |
rs770247985 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42168474 | GATGTGAGCCACCAT[A/G]CCTGGCCGAAAGACA | 10138 |
rs770275074 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42169821 | TTTTAGGAAGTAGCA[G/T]GGTTAGAGATATATA | 10138 |
rs770295129 | in-del | -/A | | | intron-variant | YAF2 | GRCh38.p7 | 12:42236540 | ACCATTCCTGTCTCT[-/A]AATTTTAAACTTAAT | 10138 |
rs770334686 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42184336 | TGTTTTTGAGACAGA[A/G]TCTTGCTCTGTCACC | 10138 |
rs770451314 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42182933 | TTACTTTTTACAAAT[C/T]GAAGGTTTGTGGCAA | 10138 |
rs770468440 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42217067 | CTAGACTATCAAAAT[C/G]GTTTCTCTGCCTCTA | 10138 |
rs770489706 | snp | C/T | 4.42468e-05 | 0.00470334 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42237764 | CGCGGCGCGGGGTCA[C/T]CAGCAGGCCGCGCCC | 10138 |
rs770521159 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42166889 | TACACTTTTGTACTT[C/T]CTGGGAAGATGATAA | 10138 |
rs770574336 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42165955 | CGGAGTCTCACACTG[C/T]CACCCAGGCTGGAGT | 10138 |
rs770626173 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42196205 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGAATC | 10138 |
rs770627707 | snp | A/C | | | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42161333 | CTGGTTCAAATAGCT[A/C]TTCTTAAGGGAAAAA | 10138 |
rs770647836 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42212270 | ATTTATCTTCAAGCT[C/G]ATATGAAGATATTAC | 10138 |
rs770682899 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42175074 | CAAAAACTTGTACAC[A/G]AATGTTCATAGCAAC | 10138 |
rs770760471 | snp | G/T | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42240166 | AAGGGGATACTTCCC[G/T]ATAAATCCACCTTAA | 10138 |
rs770802516 | snp | A/G | 1.66217e-05 | 0.0028828 | missense, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160731 | GCAGGCGGTGACTTT[A/G]TTTTCTCCTTAAAGT | 10138 |
rs770825439 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42225538 | AAGTCTTTAATCCAT[C/T]TTGAGTCAATTTTGT | 10138 |
rs770858167 | in-del | -/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42213322 | AGTGAGCTTGCAAAT[-/G]GATCCTTCCTCAGTT | 10138 |
rs770875274 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42220031 | CCTTCTCAGAGACTG[C/G]AGGACTTCTCAGAGA | 10138 |
rs770939092 | in-del | -/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42228787 | CGTCCGGGAGGGAGG[-/T]TGGGGGGTCAGCCCC | 10138 |
rs770950574 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42162053 | AATTATTTTAAATGT[A/G]TATCAAAAAAAATGG | 10138 |
rs770998921 | snp | C/T | 1.76145e-05 | 0.00296765 | missense, nc-transcript-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42161640 | TGGCTATTCTTTTTG[C/T]TAGTTGTTTCCTTTT | 10138 |
rs771023654 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42189204 | TTCAGAAAACCTGCT[A/G]GTAAATAATCAACTA | 10138 |
rs771086174 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42183124 | AGGAGCCAAGGCCCA[C/T]ACCTGTATATGACAG | 10138 |
rs771109798 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42165672 | GAGACGGGGTTTCAC[C/T]GTGTTAGCTAGGATG | 10138 |
rs771196882 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42163446 | GAGACTAGTGGTCTA[A/C]TAAATGATCATGTAA | 10138 |
rs771210971 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42196694 | ACTGTTGCAATGAAC[A/G]AAGTGTTGCTACATC | 10138 |
rs771230365 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42192500 | GGCAACACAGTGAGA[A/C]CCTGTCTCAAACAAA | 10138 |
rs771288919 | snp | A/G | | | intron-variant, missense, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42235872 | TTCCTTCTTCTTCCA[A/G]GTGCCAGGTATTCAG | 10138 |
rs771386066 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42213858 | TCTTTTATCTAATCT[C/T]AAAATTCAAACAGGG | 10138 |
rs771386997 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42205847 | TCCCCAAGTACCATT[G/T]TTGTGCATCCCTCAA | 10138 |
rs771406420 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42181706 | AGATGAAAATAATTC[A/G]CAGATGCCAGAATTC | 10138 |
rs771448043 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42221807 | CCAACAAGAAGGTTT[C/T]GAAAACAATAGTAGT | 10138 |
rs771448224 | snp | A/G | 0.000186864 | 0.0096642 | intron-variant, synonymous-codon, missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | YAF2 | GRCh38.p7 | 12:42237622 | GGTGCCCTTCCGCAC[A/G]TCGCACATCATGCAC | 10138 |
rs771523265 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42189905 | AAAACAGGTCAATAG[C/T]GTATGTATTCACTAC | 10138 |
rs771534765 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42225676 | CAGGTTTGTCGAAGA[C/T]TAGATGGTTGTAGAT | 10138 |
rs771550469 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42190760 | AGTTTTTTCTTTTTT[C/T]AGGGACAATAATTTT | 10138 |
rs771572959 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42230069 | GGAGACCATCCTGGC[C/T]AACATGGTGAAACCC | 10138 |
rs771647834 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42202566 | ATTAAGTCTGGGAGA[C/G]AGTCATCCCATGTTA | 10138 |
rs771853903 | in-del | -/A | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234181 | CTCAAATTCTGCCTC[-/A]AAAAAAAAAAGAGAA | 10138 |
rs771885094 | snp | C/T | 1.65924e-05 | 0.00288027 | missense, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160711 | CTGCAGAAGCAGCAC[C/T]AGATGCAGGCGGTGA | 10138 |
rs771885140 | snp | A/C | | | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42230795 | GTTTGGGGAGGCAGA[A/C]ATGGGTTTCAGAGAT | 10138 |
rs771890104 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42162001 | TCTAAGATATATGCT[C/G]AAACATTAGAATACT | 10138 |
rs771895002 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42214882 | GGTGGCAGGCGCCTG[C/T]GGTCCCAGCTACTCA | 10138 |
rs771978549 | snp | C/G | | | intron-variant, nc-transcript-variant, missense | YAF2 | GRCh38.p7 | 12:42212474 | AACTTATGATTTCAT[C/G]ATTCTTCATTCTATG | 10138 |
rs771979070 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42206537 | TCGCTTGAACCCAGG[G/T]GGTGGAGGTTGAAGT | 10138 |
rs771989432 | snp | C/T | 4.49045e-05 | 0.00473817 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238118 | CGAGGGCCCTGCCGC[C/T]CGCACAGTCCGGGCC | 10138 |
rs771990206 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42164661 | TAAATTGAAGCGATA[C/T]GGTAAATCTCATCAA | 10138 |
rs772039440 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42178585 | ACATATATAACTATA[C/T]CATCAAATACAGTTT | 10138 |
rs772041511 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42163720 | AAAGAAGCACAAAAC[A/G]TAAATGTATATAGTT | 10138 |
rs772110525 | snp | C/T | 1.65573e-05 | 0.00287721 | synonymous-codon, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160613 | TTCTCCATTCAATGA[C/T]GAGGCTTCTCCTCTG | 10138 |
rs772166092 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42176831 | ATGTAGCTAGGCGTG[A/G]TGCTGGGCGTCTGTA | 10138 |
rs772178716 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42185599 | CTTCAACAATCACCA[A/G]CATGATCACTCAGCA | 10138 |
rs772277612 | in-del | -/AAAT | | | intron-variant | YAF2 | GRCh38.p7 | 12:42215940 | AAAAAATAAATAAAT[-/AAAT]AAATAAATAAATAAA | 10138 |
rs772301528 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42199308 | GACCAATAGTTTAAA[C/T]CCATCAAACATAATA | 10138 |
rs772311819 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42184731 | CTTCGCCATTCTAGA[C/T]GTCATTAAGAACATT | 10138 |
rs772312093 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42195050 | TTAATATGATAGATA[C/T]GGTTTCAGCCCTTAC | 10138 |
rs772337696 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42221924 | CATTAAGGTTTCAAG[C/T]AATAAAAACTTGTCT | 10138 |
rs772399878 | snp | C/T | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42240183 | TAAATCCACCTTAAA[C/T]AGAAAATATTGTAAA | 10138 |
rs772408966 | snp | A/G | 3.18264e-05 | 0.00398901 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238187 | GTCTCCCATGGCTTG[A/G]CTATCACCGCACGCC | 10138 |
rs772413543 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42180226 | AGCAAAAACCGATTG[A/G]ATGTCATTTCCAAAA | 10138 |
rs772424622 | in-del | -/A | | | intron-variant | YAF2 | GRCh38.p7 | 12:42207736 | CTCTACTAAAAATAC[-/A]AAAAATTAGCCGGGC | 10138 |
rs772424705 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42179108 | CTTTAAGAACTTGAT[G/T]TACTTAGACTGGGAT | 10138 |
rs772463036 | snp | C/T | | | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42156913 | TATTTTCCTTACATA[C/T]GCACTCACTTTTCTG | 10138 |
rs772512017 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42182142 | AGAAGGTTAAAACTA[C/T]AAAAGCATCATTTAT | 10138 |
rs772526961 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42193562 | AGGCTAGAATCCAAT[G/T]GTGTGATCATTGTTC | 10138 |
rs772659778 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42208312 | ATGCTTGTAATCCCA[A/G]CTACTTGGGAGGCTG | 10138 |
rs772877777 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42199722 | CTAGCACTAACCAAA[A/G]ACACAGAATACGGTA | 10138 |
rs772983777 | snp | A/G | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232882 | AGTTATAAACAACAT[A/G]TATTTTTAATGAAGA | 10138 |
rs772996614 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42236813 | AGAATCAAGGAGCTC[G/T]ATAACTAAGTGCTGA | 10138 |
rs773005250 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42227528 | CGCCTCTGCCCTGCC[A/G]AGACCCCGTCTGGGA | 10138 |
rs773113233 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42193595 | TGCAGCTGCCTTGAC[C/T]TCCTGGGCTCAAGTG | 10138 |
rs773156618 | snp | A/G | 9.56099e-05 | 0.00691345 | utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238198 | CTTGGCTATCACCGC[A/G]CGCCGAGAGTCGCCG | 10138 |
rs773215199 | in-del | -/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42176522 | CCAGTTGCTTAGACC[-/G]AACACTTAGAAGCAG | 10138 |
rs773224087 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42158082 | GGTTCTGAATCTTTC[A/G]CATATTTTAACGTCA | 10138 |
rs773245712 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42185948 | CTCACGCCTGTAATC[C/T]CAACACTCTGGGGAG | 10138 |
rs773290385 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42195289 | TTTTAGCTGGCAATA[C/T]ACTATCACGTAAAGC | 10138 |
rs773342398 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42187559 | GATACAATGGCATAA[C/T]GTTTAAGAGCTTGGC | 10138 |
rs773343859 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42196573 | AAGTTGAATTATCTA[C/G]AGAGACTAAATAAGT | 10138 |
rs773350049 | snp | G/T | 4.49974e-05 | 0.00474307 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238120 | AGGGCCCTGCCGCCC[G/T]CACAGTCCGGGCCCC | 10138 |
rs773381464 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42182987 | GCGCCATTTTTCCAA[C/T]AGCATGTAAAAGTTG | 10138 |
rs773426669 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42182150 | AAAACTACAAAAGCA[C/T]CATTTATAGTTGTAT | 10138 |
rs773517297 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42202471 | CTCTATCACTATAGA[C/T]TATTTCTACTTGTTT | 10138 |
rs773531660 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42219870 | CCAGGTGATGCTAAC[C/G]CCACTGGTCTGTGGA | 10138 |
rs773646919 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42202700 | TTGGAGTGCAATGGC[A/G]TGATCTCGGCTCACT | 10138 |
rs773652077 | snp | C/T | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239000 | TGTTTTAATTCCAAA[C/T]GCGCCCTTTTGGCCT | 10138 |
rs773688239 | in-del | -/ATT | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232320 | AAATAACATCTTCAA[-/ATT]ATTATTATAAAAACA | 10138 |
rs773695259 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42173802 | GAAGAGAGCACTGAA[C/T]AAAACTTGCTTTTAT | 10138 |
rs773735698 | snp | A/G | 6.62899e-05 | 0.00575678 | intron-variant | YAF2 | GRCh38.p7 | 12:42161779 | TCCTGTGTGCATGTT[A/G]AAAAGAAAGGTATTT | 10138 |
rs773741974 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42202419 | TCACGATCCTTACCA[A/G]TCAGTACCATGCTTC | 10138 |
rs773764716 | in-del | -/C | 0.000162298 | 0.00900682 | intron-variant, utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42235782 | AAAAAATGTCAGGGG[-/C]CCCCATGTGGGCCTC | 10138 |
rs773820929 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42168475 | ATGTGAGCCACCATG[C/T]CTGGCCGAAAGACAG | 10138 |
rs773832501 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42218915 | AGAGAAAGGGCTTTC[A/C]AGAAAGAAAGCTTCA | 10138 |
rs773891912 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42220281 | TTATACTTCCTTAAA[C/T]CTTTAATGTATACAT | 10138 |
rs773950316 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42163607 | ACACAACTATTCCAT[C/T]TTTATTCTTATTTTA | 10138 |
rs773963460 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42166893 | CTTTTGTACTTTCTG[G/T]GAAGATGATAAAACA | 10138 |
rs774004414 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42187732 | TTAATAAATAATAAC[G/T]ATTTGTTCTTATTCT | 10138 |
rs774039824 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42201253 | TGAATAGTAATCAAC[C/T]GCTAGATAACAGAGT | 10138 |
rs774138829 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42208630 | ATTAAATAAATTCCA[C/T]GAATTAATAGTCTTA | 10138 |
rs774160847 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42193828 | TATCACAGCAGATGA[C/T]GGCTCCATGCATGTT | 10138 |
rs774180197 | in-del | -/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42170037 | ACCACACCTGGGTAA[-/T]TTTTTTTATTTTTTG | 10138 |
rs774434876 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42183396 | CAGACCAAAAGCTAG[A/G]CCTTTTGTGCCAGTT | 10138 |
rs774490898 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42196763 | AGTGAAAGCTCTTGA[C/T]TTTTTAATGATAGCC | 10138 |
rs774540247 | in-del | -/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42209810 | ATGCATAATTTTTTG[-/T]TTTTTGAGACAGAGT | 10138 |
rs774546623 | snp | A/G | 1.6654e-05 | 0.00288561 | intron-variant, synonymous-codon, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42237694 | GTCCCAGTAACCCTC[A/G]TCCGAGGACGGCTTC | 10138 |
rs774551532 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42198106 | AGTGAAATGTTGGGC[C/T]TCACCTTATAAAAAA | 10138 |
rs774557084 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42229779 | GAATGTTGCAGGTAA[C/T]TGTAACACCATGGTA | 10138 |
rs774573516 | snp | C/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233364 | TTCATTTCTAAATAT[C/T]TGCTATCTGAATTAA | 10138 |
rs774583675 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42169222 | TTGACTTCTGTGTAT[C/T]ATGACATTATTTAAC | 10138 |
rs774603912 | snp | A/C/G | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42240167 | AGGGGATACTTCCCG[A/C/G]TAAATCCACCTTAAA | 10138 |
rs774640036 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42179040 | CCTGTGAAACAAAGC[A/G]AGACCCTCTCTCTTT | 10138 |
rs774657183 | snp | C/T | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239155 | TCTACGTCAACATAC[C/T]AAAGGTCCTCATACT | 10138 |
rs774669248 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42203674 | TCTTATAAATTGATA[A/C]AATTTTCAAATATTG | 10138 |
rs774671597 | snp | C/T | 1.71384e-05 | 0.00292727 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238109 | AGCCCTGCACGAGGG[C/T]CCTGCCGCCCGCACA | 10138 |
rs774683032 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42218608 | GGGGATTTTAGACTT[C/T]AAGGATGTTGATTTT | 10138 |
rs774760935 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42221886 | TCAAGATCTTCCCTC[C/T]GAAGACGCTCTTATC | 10138 |
rs774764843 | in-del | -/AAAC | | | intron-variant | YAF2 | GRCh38.p7 | 12:42170650 | CCCTGTCTCTACTAA[-/AAAC]AAACAAACAAACAAA | 10138 |
rs774829285 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42191728 | ATTACAAACTGTGGT[A/G]TTCATTTTTCCCCAC | 10138 |
rs774838790 | snp | G/T | 3.38656e-05 | 0.00411481 | synonymous-codon, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160823 | CACATTTTTCAATCT[G/T]GGCCTAAACATAAAA | 10138 |
rs774867190 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42191168 | CATTGCTGTTAATGT[C/T]TAAAGTACTCCCATT | 10138 |
rs774887742 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42230130 | GGTATGGTGGCACAC[C/G]TCTGTAATCCCAGCT | 10138 |
rs774920835 | snp | C/T | | | downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42156777 | ATCAGTGATTTTTGT[C/T]ATTGGTAACTGTTCT | 10138 |
rs775035187 | in-del | -/AAATAAATAAAT | | | intron-variant | YAF2 | GRCh38.p7 | 12:42215932 | TCCAGCTCAAAAAAT[-/AAATAAATAAAT]AAATAAATAAATAAA | 10138 |
rs775122242 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42170410 | GCTCATTTATCTTGC[A/G]TATCTTAATGATAAC | 10138 |
rs775143712 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42175334 | GACAGAAAGCAGATC[A/T]GTAGTTGCCTAGCAA | 10138 |
rs775168969 | snp | C/T | 3.30808e-05 | 0.00406686 | intron-variant | YAF2 | GRCh38.p7 | 12:42161769 | GGTCGAGGTTTCCTG[C/T]GTGCATGTTAAAAAG | 10138 |
rs775182133 | in-del | -/TC | | | intron-variant | YAF2 | GRCh38.p7 | 12:42197015 | TCTGTTTTGTTCACT[-/TC]TCAGAAAGTACTTCA | 10138 |
rs775217665 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42184817 | TGATGCCAATTATCA[C/T]GGATGACTGAATGGT | 10138 |
rs775269526 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42198231 | AATTATAATCCTACC[A/T]ACTCTAGCCCTCATA | 10138 |
rs775333725 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42212492 | TCTTCATTCTATGGA[A/G]ACAAAGAAAGTGTAT | 10138 |
rs775345138 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42188274 | AATAGAATAAATCAA[G/T]GTATTCAAAAATATT | 10138 |
rs775377376 | in-del | -/AC | | | intron-variant | YAF2 | GRCh38.p7 | 12:42191423 | TTTGACCATCCATTT[-/AC]TTCCAATCCCCCTAG | 10138 |
rs775394244 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42196953 | GAATGGAGAGTTACT[A/G]AAGATTTAAGGAGGG | 10138 |
rs775487352 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42164709 | AAATCCATACATATT[A/G]TGAATCTGTTGATAC | 10138 |
rs775488299 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42214153 | TTACCCACTTGCTCA[C/T]CTTCATCTGATGCCA | 10138 |
rs775497222 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42206103 | TCTCTGTGCTTGTCC[A/G]GAGGAGTACTCATTT | 10138 |
rs775538720 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42163725 | AGCACAAAACATAAA[C/T]GTATATAGTTCAATT | 10138 |
rs775541839 | snp | A/C | | | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42230942 | TGGGCCACTGAGTTA[A/C]ACAACTAGGATATTA | 10138 |
rs775557728 | snp | A/G | 1.6777e-05 | 0.00289624 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160584 | GAAATTGGAGAAAAT[A/G]AACTTTAATGAGATT | 10138 |
rs775654072 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42171496 | AACGTGGTATGACCC[C/T]ATCTCTTTAAATTAA | 10138 |
rs775732242 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42180230 | AAAACCGATTGGATG[C/T]CATTTCCAAAATTAG | 10138 |
rs775747091 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42206816 | ATTCCCATTTTAGAA[C/T]TGGAGAAATTGAAGC | 10138 |
rs775747236 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42223784 | ACGGGAACAGAAAAC[C/G]TAACACCGCATGTTC | 10138 |
rs775804349 | snp | A/G | 0.000324412 | 0.0127319 | intron-variant, synonymous-codon, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42235949 | GGTTCCTCTAACCCC[A/G]AGACTGGCTGTGGAG | 10138 |
rs775808104 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42194322 | CCTCCAGCCTTGCAA[C/G]CTCTATGATACAAGT | 10138 |
rs775857776 | snp | A/C | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42235154 | AGTCTGACCCAAAGG[A/C]TTCAAATCCCATCTG | 10138 |
rs775886057 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42182335 | CTATTACATGGTAAC[A/C]GGTATTTTTGCTTTA | 10138 |
rs776000784 | snp | C/T | 5.212e-05 | 0.00510463 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42237654 | TGAAGGCCTCGGCGC[C/T]GTTCCGGAAGGTGCA | 10138 |
rs776060567 | in-del | -/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42213812 | AAACATACATCAAGG[-/T]TATTAGTAACAGTAA | 10138 |
rs776191195 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42208373 | GGAGGTTGCAGTGAA[C/T]GGATATCATGCCACT | 10138 |
rs776235689 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42187112 | ATTATTTTAAGTACT[A/T]ATTATTATTACTATT | 10138 |
rs776301406 | snp | C/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232590 | CAGATAGACAGGAGG[C/T]GGCTCAGGAACCATG | 10138 |
rs776310714 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42191439 | CTTCCAATCCCCCTA[A/G]TAATTTTGTTCTAGT | 10138 |
rs776352129 | in-del | -/TG | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42235199 | AAATCATTAGCAAAC[-/TG]CATCCTTCTGCTCTG | 10138 |
rs776386278 | snp | C/T | 0.000215088 | 0.0103681 | synonymous-codon, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160631 | GGCTTCTCCTCTGGG[C/T]GAAGATGACCTGGAC | 10138 |
rs776487420 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42185978 | GTCCGAAGCAGGTGG[C/G]TAATCTGAGGTCAGG | 10138 |
rs776516428 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42222499 | TCACCAGCCATATAG[G/T]GGCGGTTTGATGAGC | 10138 |
rs776540853 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42208196 | ACTTTGGGAGGCCGA[A/G]GCGGGCAGATCACTT | 10138 |
rs776547239 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42191225 | TATATCGTTTTCACT[A/C]TAAACACTTTTGTGC | 10138 |
rs776564080 | snp | G/T | 1.70921e-05 | 0.00292331 | missense, nc-transcript-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42161661 | GTTTCCTTTTCACTT[G/T]TTTCTTTTTCTACTT | 10138 |
rs776582702 | snp | A/G | 1.66194e-05 | 0.00288261 | synonymous-codon, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160757 | AAAGTCTGTAATAAT[A/G]ACTGTCAGATCTCCA | 10138 |
rs776679285 | in-del | -/ACAC/ACACAC | | | intron-variant | YAF2 | GRCh38.p7 | 12:42218191 | TACTAGGAAACACAC[-/ACAC/ACACAC]ACACACACACACACA | 10138 |
rs776757367 | in-del | -/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42179156 | TATTTGTTTAGTTGT[-/G]AAGTTTCCAAGATGA | 10138 |
rs776806096 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157240 | ACTGAGGAGGGCAAA[A/G]AGAACAGAACACAAG | 10138 |
rs776857052 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42185820 | GAAACCAAAAACTTC[C/G]TATGACTTGCTTTGT | 10138 |
rs776997236 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42181816 | AATTTATAACTGTGA[C/T]GTCTATGCCAAGTAC | 10138 |
rs777018261 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42168399 | GTTGGTTAGGCTCGT[C/G]TTGAACTCCTGACCT | 10138 |
rs777045990 | snp | A/G | 0.000166653 | 0.00912681 | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42237632 | CGCACATCGCACATC[A/G]TGCACTTGAAGGCCT | 10138 |
rs777064203 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42199903 | CTTTGGCACATAACA[A/G]TTCAAGGTTATACAG | 10138 |
rs777067965 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42217221 | TGCAGGTAGCTTAGA[C/T]TGATGTAAGTTCTTC | 10138 |
rs777196655 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42166516 | TTGCAAAATATTGCA[C/T]GATAAAATCCTTTCT | 10138 |
rs777198689 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42182627 | GTTGCTTTAAACCTC[A/C]GTATGTAATTGGCAA | 10138 |
rs777199618 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42181143 | ACAGCACATTCAGAG[C/T]GGGACAAGCTGTCCT | 10138 |
rs777233919 | snp | A/G | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234883 | GTTTCAGCTACTTGG[A/G]AGGCTGAGGTGGGAG | 10138 |
rs777262139 | snp | A/G | 0.000111588 | 0.00746872 | intron-variant, synonymous-codon, missense, nc-transcript-variant, upstream-variant-2KB, utr-variant-5-prime | YAF2 | GRCh38.p7 | 12:42237601 | GCCCGGGACTCACCG[A/G]GTGGAGGTGCCCTTC | 10138 |
rs777323650 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42181180 | GAGGTTACTGAAGTA[A/C]ATAATACTTGATTTG | 10138 |
rs777326445 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42195146 | GGAGAAGTCCAAAAT[A/G]GATAAAGAAATCTAG | 10138 |
rs777363556 | snp | A/G | | | intron-variant, missense, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42235951 | TTCCTCTAACCCCAA[A/G]ACTGGCTGTGGAGTA | 10138 |
rs777366099 | in-del | -/TTCTT | 0.000194951 | 0.00987104 | intron-variant | YAF2 | GRCh38.p7 | 12:42199279 | AACACTATGTACACA[-/TTCTT]TGGAACAGAATTTGA | 10138 |
rs777401187 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42195736 | TAGAGAATAGACCAT[C/T]GAACCAGTCATGGTG | 10138 |
rs777451764 | snp | C/T | 2.89691e-05 | 0.00380575 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42237740 | CTGCAGGACACAACC[C/T]GGACACGACGCGGCG | 10138 |
rs777484845 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42224905 | CCAGTAATGAGACTG[C/T]TGGATCAAATGGTAT | 10138 |
rs777543437 | in-del | -/TA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42168024 | AAGTTATAAAATACT[-/TA]TTAAGTAATATTTAT | 10138 |
rs777556866 | in-del | -/ACACAC | | | intron-variant | YAF2 | GRCh38.p7 | 12:42218186 | TCAGGCTACTAGGAA[-/ACACAC]ACACACACACACACA | 10138 |
rs777595722 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42222472 | AATTATTTGACTAGC[C/G]GACCATCTTCCTCAC | 10138 |
rs777612894 | in-del | -/AGAAA | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234203 | AAAAGAGAAAAGAAA[-/AGAAA]AGAAAAGAAAAGAAA | 10138 |
rs777722003 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42213597 | TTTTCCTTCCTTAGG[A/G]AAAGTCATCCTTTTT | 10138 |
rs777729086 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42203923 | TAATTACAAATATCA[C/G]CATTAAAACTATTCC | 10138 |
rs777783455 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42178214 | GGATCTGTGATCCTA[C/T]CGCACTTGTTTTCAA | 10138 |
rs777788729 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42198538 | TTGCAGTGAGCTGAG[A/G]TCGTACCACTGCACT | 10138 |
rs777803140 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42214606 | TCTGATTAAATGCCA[C/T]CCACTCAGAGAAGCC | 10138 |
rs777876339 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42171661 | TTTCTCATTACAAAA[A/G]TCTCATATCTGGCTG | 10138 |
rs777894024 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42163146 | TCCAAGTTATGCTGA[C/T]GTCTCTGGGGACCAC | 10138 |
rs777959288 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42230591 | TCCAATAGTTCATGA[C/T]AGAAGTGATATGGGC | 10138 |
rs778009962 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42226589 | GGACCACTTCAACCT[A/G]GGAGGTTGAGGCTGC | 10138 |
rs778176978 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42207621 | GTGTAGGCTGGGCAC[A/G]GTGGCTCATGCCTGT | 10138 |
rs778214607 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42170922 | TTCCCCTAATATCCG[C/T]TCTAAATGTTGAATG | 10138 |
rs778229650 | in-del | -/AAA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42206298 | AATATGCTCTTAGTT[-/AAA]AAAAAAAAAAAAAAA | 10138 |
rs778277408 | snp | G/T | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42240035 | TAAATAAATAACATT[G/T]TTTTGAGCACTATGT | 10138 |
rs778316415 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42199023 | TGTTTAATTTCATGT[A/G]ACTATTTTAACATTT | 10138 |
rs778329740 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42169465 | GTCCCCCAGGCTGGA[A/G]TGCATTGGCACAATC | 10138 |
rs778363976 | snp | A/G | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238775 | AGCTACCCAGCCCCC[A/G]CCTGCAGTATACCGG | 10138 |
rs778396868 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42184456 | CTGGGACTACAGGCA[G/T]GTGCCACCACGCCTG | 10138 |
rs778419948 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42218453 | ATTGCCTATTTTATT[A/G]TGTAAAGTGGCCTAT | 10138 |
rs778440909 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42204080 | TCTAAAAAAACCAAC[C/G]AAACAAAAAAAAATC | 10138 |
rs778454360 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42168332 | TACAAGTGTGCACCA[A/C]CATGCCCAGCTAATT | 10138 |
rs778467174 | snp | A/T | 0.000166293 | 0.00911694 | intron-variant, utr-variant-3-prime, utr-variant-5-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42235716 | CTCCTCAAGTAATGT[A/T]TCCACCACTAAAAAT | 10138 |
rs778565791 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42225404 | GCTTTTGTTGCCACT[A/G]CTTTTGGTGTTTTAG | 10138 |
rs778606310 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42230716 | TGAGACAATGACAGT[C/T]TCTAGCTGAGGTTCC | 10138 |
rs778691185 | in-del | -/TTAT | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234663 | AATTTGAACTTAATA[-/TTAT]TTAAAGAAAAAAAAT | 10138 |
rs778818702 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42185528 | TGAAAGGAAGAGTTA[A/C]TCAATGTGGAAAACT | 10138 |
rs778862753 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42192147 | GAATATGGAGAAAAA[C/T]TACATGAGATAAAAC | 10138 |
rs778884199 | snp | A/C | 0.000220706 | 0.0105026 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42161606 | ATAAAACACTCTTCA[A/C]ATTTACCTGGTTTTC | 10138 |
rs778919527 | in-del | -/AAGAAAGAG | 0.000848536 | 0.0205803 | intron-variant | YAF2 | GRCh38.p7 | 12:42230262 | TCCTTCAAGAAAGAA[-/AAGAAAGAG]AAGAAAGAGAAGAAA | 10138 |
rs778926462 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42200379 | CCTTAAAGAGAGAGG[C/T]TGAAAACTATTCACC | 10138 |
rs778929090 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42165229 | GTGTTGTGATAGAGA[A/C]AACAGGAGGAGGAGT | 10138 |
rs778964786 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42190658 | TAATTTTATTTGTAT[A/C]CTGTATGTTATTCAT | 10138 |
rs778979538 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42199124 | TTAAGGTGAAAAACA[C/G]TGACAGCTTACCAGA | 10138 |
rs778986773 | snp | A/G | 0.000584852 | 0.0170905 | intron-variant | YAF2 | GRCh38.p7 | 12:42205876 | AAATTTTGATACAAC[A/G]CTTTTGTTGTGATTT | 10138 |
rs778987179 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42175690 | GACCATCCTGGCCAA[C/T]GAGATCGCACCACTA | 10138 |
rs779075583 | snp | C/G | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233170 | ATACTAGTGTAACAT[C/G]TAGCACTCTTTCTAC | 10138 |
rs779095182 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42193172 | ATACAAAAATTAGCC[A/G]GGTGTGGTGGTGCAT | 10138 |
rs779102846 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42209470 | TCAGGAGGCTGAAGT[A/G]GGAGGATGGCTTGTG | 10138 |
rs779116777 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42169406 | GTTCTTAATCTCTTC[A/T]CTTTAATTTTTCTTT | 10138 |
rs779223139 | in-del | -/AC | | | intron-variant | YAF2 | GRCh38.p7 | 12:42212539 | ATAGTCTAGTAACTA[-/AC]TCACCACTGAATAAA | 10138 |
rs779268680 | in-del | -/ATG | | | intron-variant | YAF2 | GRCh38.p7 | 12:42214671 | TTGCCACACTCTGCA[-/ATG]ATTTTTTTTTGGTAT | 10138 |
rs779339622 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42207911 | GACAAACAAAAAACT[G/T]GTAAGTTTATTCATA | 10138 |
rs779351841 | snp | C/T | 6.39386e-05 | 0.00565378 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238171 | TGGTGGGGCTCTTCT[C/T]GTCTCCCATGGCTTG | 10138 |
rs779355236 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42158049 | ATGAAACAGAGAAAA[A/T]CATGTACCCTAAACC | 10138 |
rs779383020 | in-del | -/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42176140 | TATCCCACTTACTCA[-/G]GAGGCTGAGGCAGGA | 10138 |
rs779454719 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42186483 | GAGTTTGAGATCAGC[A/G]TGACCAACGTGGTGA | 10138 |
rs779550613 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42223576 | TATGTTGCCCAGGCT[A/G]GTCTTGAACCCTAGG | 10138 |
rs779567224 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42192260 | TGCCTGTAATCCCAA[C/T]AGTTTGGGAAGCTGA | 10138 |
rs779613394 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42201900 | TTAAACTCAAGTTTT[C/G]CTTTTTGAGGCAACA | 10138 |
rs779678135 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42170857 | TATCATTATTACCCA[C/T]ATTCTTCAAGAATAA | 10138 |
rs779725640 | snp | A/G | 0.000280191 | 0.0118329 | intron-variant, nc-transcript-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42210408 | AGATCCACCTCTCTT[A/G]CCCTTCTGTTCAGCA | 10138 |
rs779730625 | snp | C/T | 0.000163359 | 0.00903619 | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238692 | GTTCGGAGGCCTGTC[C/T]AGGTCTGGACAGAAG | 10138 |
rs779742148 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42214978 | CACTGCACTCCAGCC[C/T]GGGCAACAGAGTGAG | 10138 |
rs779768566 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42179519 | GTGACTGAAACACAT[C/G]AAATCTGAAGGTCTA | 10138 |
rs779793369 | snp | A/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232468 | TAAAATTTACCCATA[A/T]ACAATTAACCAGTGT | 10138 |
rs779927478 | snp | C/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42233736 | CAGGTTGGTCTCAAA[C/T]TCCTGGCCTCAAGAA | 10138 |
rs779958993 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42172841 | TACTGACAGATACTA[A/C]AACATGGATGAGCCT | 10138 |
rs779968033 | in-del | -/A | | | intron-variant | YAF2 | GRCh38.p7 | 12:42203067 | AAGGTCATTTTCCAC[-/A]AAAAAAAAAAAAAAT | 10138 |
rs780068808 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42219396 | GGATGAGCTGTATGG[A/T]TGAAGGAATGTACAG | 10138 |
rs780105637 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42178604 | CAAATACAGTTTGCT[A/C]CCATTTTCATTTTTA | 10138 |
rs780116391 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42201808 | CACTCCTGACCTCAA[C/G]TGAACCATCTGCCTT | 10138 |
rs780120053 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42186768 | TTAAATTTGCCAATG[C/T]CTCAATTTGGAATAT | 10138 |
rs780137858 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42171617 | CTACAAGCAAAAGGG[C/T]CAGAACTGGGTATAT | 10138 |
rs780231182 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42195930 | GGCAGAGACAGAGAA[C/T]GGGAGGACAGGCCAG | 10138 |
rs780235760 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42158146 | GTGTGGAAGTGTACT[C/T]GAAGTAGGGTGAAAC | 10138 |
rs780249567 | snp | A/G | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42239505 | GTGCTGTTTCTGTCC[A/G]TCTTTCTAGGTTTAC | 10138 |
rs780250002 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42200488 | CAGTATCAAGAATAA[A/T]TGAAGATTAAAACAA | 10138 |
rs780307219 | snp | A/C | 1.92911e-05 | 0.00310566 | intron-variant, downstream-variant-500B | YAF2 | GRCh38.p7 | 12:42161566 | GGTTAAAAAAATTAA[A/C]TGGTTTTATTATTTC | 10138 |
rs780404212 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42158295 | TTTCTGCATCCAGAG[A/G]AAACATCTGATATTA | 10138 |
rs780470180 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42195073 | GCCCTTACAGTTCAG[C/T]GTGAGAAACAAGAAA | 10138 |
rs780535408 | snp | C/T | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42235335 | TTTTGCTTCTCAACA[C/T]CGTTCTGCAGTCCTT | 10138 |
rs780537969 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160441 | TGCAATAAAATCTAA[A/C]AAATTCTAACAAATT | 10138 |
rs780548997 | snp | A/C | 1.83199e-05 | 0.00302648 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42237775 | GTCACCAGCAGGCCG[A/C]GCCCGGTGCCCGGGC | 10138 |
rs780563600 | snp | A/G/T | 0.000113391 | 0.00752892 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238143 | CGGGCCCCGGGGCCC[A/G/T]GGCGCTGTTACCTGG | 10138 |
rs780590926 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42174378 | CCTTCCCTTCCTGAA[A/G]AACTTTTTTCACTCA | 10138 |
rs780614243 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42185368 | TGAACACAGTTTAAA[C/T]GACAACAAAGGATTT | 10138 |
rs780690041 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42226217 | GTCAAGAAACACTTC[A/G]TTTTTAGCTATATTA | 10138 |
rs780690220 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42209672 | ATATGACATCTGCAT[A/G]AATTTTACAATATAA | 10138 |
rs780698256 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157271 | AAGCATCCTCACTTC[A/G]TAACAACCCACTCTT | 10138 |
rs780717643 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42179697 | GCTGAGGTGGGAGAA[C/T]TGCTTGAGCCCAGGA | 10138 |
rs780738596 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42204922 | AGGATAGAGGGTTAG[A/G]AGAGATGAAAATGTT | 10138 |
rs780742989 | snp | C/G | 3.59861e-05 | 0.00424167 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238148 | CCCGGGGCCCGGGCG[C/G]TGTTACCTGGTGGGG | 10138 |
rs780764777 | snp | C/G | 3.32187e-05 | 0.00407532 | intron-variant, upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42237754 | CCGGACACGACGCGG[C/G]GCGGGGTCACCAGCA | 10138 |
rs780913305 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42166356 | GCTTCAGAATTACCA[C/T]TTTCATTTGTAGATG | 10138 |
rs780972594 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42181055 | CTCTGGGCAACTGAA[G/T]CTTTATATATTACAT | 10138 |
rs780989532 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42202165 | CCTCCCGCCAAGGAA[C/T]GCCATTTCTAGCCTT | 10138 |
rs781064674 | in-del | -/A | | | intron-variant | YAF2 | GRCh38.p7 | 12:42207319 | CTTCCTTCATTTCTG[-/A]AAAAGAAAGCAATAA | 10138 |
rs781073465 | in-del | -/GCAA | | | intron-variant | YAF2 | GRCh38.p7 | 12:42185176 | GAGCCAGACTTTGTC[-/GCAA]ACAAACAAACAAACA | 10138 |
rs781137835 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42217780 | CAATACACTGTGTAA[A/C]TATATCATCACTTTT | 10138 |
rs781149205 | in-del | -/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42218806 | AGTCGATTATGTAGC[-/T]TCTGAGCCTTACTAA | 10138 |
rs781163670 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42165641 | GCTAATTTTTTTTTA[C/T]TTTTTATTTTTAATA | 10138 |
rs781184857 | snp | C/T | | | missense, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160768 | TAATGACTGTCAGAT[C/T]TCCAACAGTAACTTC | 10138 |
rs781189785 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42190300 | AGTGAGCTGTGACAG[A/C]ACCATGGCACTCCAC | 10138 |
rs781217933 | snp | C/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42221868 | CTCTCTACTTACAAT[C/G]TCTCAAGATCTTCCC | 10138 |
rs781222842 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42195343 | ATCTTAAGAATGAAA[C/T]TGTGGCATTAAACAT | 10138 |
rs781262583 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42216639 | TCTTACCCACTCCTA[C/T]AGCTTCAACTCAAAT | 10138 |
rs781300806 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42187468 | TTATTGAAGATGTAA[C/T]CTTTTTTTTTTTAAA | 10138 |
rs781312211 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42174539 | GATACCTCTTATCTA[C/T]GCTAACCCTCCAGAC | 10138 |
rs781317651 | snp | A/T | 0.00020949 | 0.0102324 | intron-variant | YAF2 | GRCh38.p7 | 12:42205916 | TATTTTGTAATTTCC[A/T]TTTTTTTAATTCTTG | 10138 |
rs781431037 | snp | G/T | 3.43277e-05 | 0.00414278 | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160558 | TTGCATGGTAGGACA[G/T]AAGTGACTAAGAAAT | 10138 |
rs781557695 | snp | C/T | 1.65611e-05 | 0.00287755 | missense, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42160686 | CTAGAGCCGCTTTGA[C/T]TGTGTTGATCTGCAG | 10138 |
rs781571902 | snp | A/G | | | upstream-variant-2KB | YAF2 | GRCh38.p7 | 12:42238798 | TATACCGGGGGGAAG[A/G]CGGGAACCAACACGC | 10138 |
rs781640869 | in-del | -/ATG | | | intron-variant | YAF2 | GRCh38.p7 | 12:42236450 | ATATACAAAAAGCAT[-/ATG]ATGATTTACAAAAAA | 10138 |
rs781651875 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42184157 | AGATAAAAAGATTCC[C/T]TTCAAAATATTACTG | 10138 |
rs781677268 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42163040 | CAGAATCACCAAGAA[A/G]GCTTGTTTAGCTTGC | 10138 |
rs781682660 | snp | A/G | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42232129 | TGTAATAAAATTAGT[A/G]AATTTTTCTGCTTCA | 10138 |
rs781697848 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42197686 | TAAACAATAATCAAC[A/G]TAAGAAAACATGTAA | 10138 |
rs781719488 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42213045 | TGGTATAAGCTAATA[C/T]AAAAGATGTCATTAA | 10138 |
rs781762396 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42196332 | GCACATCACCTATAA[A/G]TGGGTGGCAAATATG | 10138 |
rs796075307 | snp | A/C | | | intron-variant | YAF2 | GRCh38.p7 | 12:42175719 | TACACTCCAGCCTGG[A/C]GACAGAGCAAGACTC | 10138 |
rs796095908 | in-del | -/A | | | intron-variant | YAF2 | GRCh38.p7 | 12:42212046 | TCTCAAAAAAAAAAA[-/A]GTCTTTAACCATTTG | 10138 |
rs796118048 | in-del | -/TTG | | | intron-variant | YAF2 | GRCh38.p7 | 12:42205918 | TTTGTAATTTCCATT[-/TTG]TTTTTAATTCTTGAA | 10138 |
rs796126593 | in-del | -/A | | | intron-variant | YAF2 | GRCh38.p7 | 12:42171814 | CAAAAAAAAAAAAAA[-/A]TTGGCCAGGTGTACT | 10138 |
rs796134440 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42179638 | TACAAAAAATATAAA[A/G]ATGAGCCAGGCGTGG | 10138 |
rs796162997 | in-del | -/A | | | intron-variant | YAF2 | GRCh38.p7 | 12:42229436 | TAAAAAAAAAAAAAA[-/A]CATTTAAATATCTAC | 10138 |
rs796196597 | in-del | A/GAG | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234192 | CTCAAAAAAAAAAAG[A/GAG]AAAGAAAAGAAAAGA | 10138 |
rs796230181 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42159127 | AGACAGTACCACTGT[A/G]CCTGTAAAAAGTACT | 10138 |
rs796300352 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42192483 | CACTGCACTCTAGCC[C/T]GGGCAACACAGTGAG | 10138 |
rs796370971 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42204916 | TGCCTAAGGATAGAG[A/G]GTTAGGAGAGATGAA | 10138 |
rs796480963 | in-del | AG/GAGAAAAGAAAAGAAA | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234192 | CTCAAAAAAAAAAAG[AG/GAGAAAAGAAAAGAAA]GAAAAGAAAAGAAAA | 10138 |
rs796501596 | in-del | -/CTTT | | | intron-variant | YAF2 | GRCh38.p7 | 12:42169874 | TTTTCTCTCTCTCTC[-/CTTT]CTTTTTTTTTTAAGA | 10138 |
rs796502948 | in-del | -/TTTCCCATTC | | | intron-variant | YAF2 | GRCh38.p7 | 12:42220117 | GAAAAAGTCTACTTT[-/TTTCCCATTC]TTCCAATGAGAGATA | 10138 |
rs796517496 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42203375 | TTCTTTTAATATTTC[C/T]AGGGAGCATCTCATC | 10138 |
rs796531013 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42211942 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 10138 |
rs796659751 | in-del | -/AGAGAAAAGAAAAG | | | intron-variant, utr-variant-3-prime | YAF2 | GRCh38.p7 | 12:42234191 | GCCTCAAAAAAAAAA[-/AGAGAAAAGAAAAG]AAAAGAAAAGAAAAG | 10138 |
rs796688830 | multinucleotide-polymorphism | AA/TG | | | intron-variant | YAF2 | GRCh38.p7 | 12:42188729 | TCTAAGTATTCACAT[AA/TG]ACAATTTTATTATGT | 10138 |
rs796711790 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42175876 | AAAACAATTGATCTA[C/T]ACACAGATATTAAAA | 10138 |
rs796810538 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42182973 | CAGCAAGGCTATTGG[C/T]GCCATTTTTCCAACA | 10138 |
rs796823149 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42236952 | TAAAGTCTGAAAATA[A/G]GCAGAGATCTTTTCA | 10138 |
rs796831787 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | YAF2 | GRCh38.p7 | 12:42157115 | GCAATTTATAAAGAA[A/C]ACAGATTTATTTTGG | 10138 |
rs796910096 | snp | C/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42162021 | ATTAGAATACTGTTA[C/T]GTAAATCAACATAAG | 10138 |
rs796938812 | snp | G/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42209591 | AAAAAAAAAAAAAAG[G/T]GCTAGACAATTAATA | 10138 |
rs796956610 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42164262 | GCCCAAATAGAAGGT[A/G]TAAGTTTTGCAGTCT | 10138 |
rs796962743 | in-del | -/A | | | intron-variant | YAF2 | GRCh38.p7 | 12:42176229 | AAAAAAAAAAAAAAA[-/A]TCCACCTGGATGTCT | 10138 |
rs796980551 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42163776 | TGCTCTCTAGGAGCT[A/G]AAGAGCTTTCACTGA | 10138 |
rs796988954 | snp | A/T | | | intron-variant | YAF2 | GRCh38.p7 | 12:42176978 | GTCTCAAAAAATAAA[A/T]AAATAACATCCCTCA | 10138 |
rs797018589 | snp | A/G | | | intron-variant | YAF2 | GRCh38.p7 | 12:42188382 | AAATATATATATTTT[A/G]CTTTTTTTTTTTTTT | 10138 |
rs797021813 | in-del | -/CTC | | | intron-variant | YAF2 | GRCh38.p7 | 12:42205376 | TTGCTGCTGCTTCTT[-/CTC]TTTTTTTTTTTTTTT | 10138 |