SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13636 | snp | G/T | 0 | 0 | utr-variant-5-prime, synonymous-codon | LYN | GRCh38.p7 | 8:55880028 | GGGCGCGACGGGGCG[G/T]CCCAGCAGGACCTGC | 4067 |
rs167999 | snp | A/G | 0.272188 | 0.249013 | intron-variant | LYN | GRCh38.p7 | 8:55880126 | CTCTGCGCGAGCCCA[A/G]GGGTGGGCGCGGGCA | 4067 |
rs170783 | snp | C/T | | | intron-variant | LYN | GRCh38.p7 | 8:55911223 | atatatatatatata[C/T]acacacacacacgta | 4067 |
rs179692 | snp | C/T | | | intron-variant | LYN | GRCh38.p7 | 8:55911157 | atatatgtatatgta[C/T]atatatatacacgtg | 4067 |
rs182832 | snp | G/T | 0.247337 | 0.249986 | upstream-variant-2KB, utr-variant-5-prime | LYN | GRCh38.p7 | 8:55878302 | TTAGGGAGTTGGGGA[G/T]CTGGTTGCAAGCTCA | 4067 |
rs182833 | snp | C/T | 0.252421 | 0.249988 | intron-variant | LYN | GRCh38.p7 | 8:55880265 | GCACCGCCTCTGGGC[C/T]CCGGCGGCGAAGGCT | 4067 |
rs333612 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | LYN | GRCh38.p7 | 8:55912212 | GGGGCACACAGAAAT[C/G]TGTTACACGGTGAAA | 4067 |
rs333614 | snp | G/T | 0.250732 | 0.249999 | intron-variant | LYN | GRCh38.p7 | 8:55884176 | GCAATCTCAGCTCAC[G/T]GCAATCTCCGCCTCC | 4067 |
rs333615 | snp | A/G | 0.261884 | 0.249717 | intron-variant | LYN | GRCh38.p7 | 8:55886397 | ggcatgcaccaatgc[A/G]ccaccatgcccggct | 4067 |
rs333616 | snp | C/T | 0.356597 | 0.226135 | intron-variant | LYN | GRCh38.p7 | 8:55888438 | TAGTATGAAGCTAAT[C/T]TTTTTGTCCATCACA | 4067 |
rs333617 | snp | C/G | 0.373799 | 0.217195 | intron-variant | LYN | GRCh38.p7 | 8:55889048 | tttgagatggggtct[C/G]actctgtcgcccagg | 4067 |
rs333618 | snp | G/T | 0.199564 | 0.24486 | intron-variant | LYN | GRCh38.p7 | 8:55889248 | tttgagacCAGGCTG[G/T]AACcccaggcaggag | 4067 |
rs333619 | snp | A/T | 0.498323 | 0.0289051 | intron-variant | LYN | GRCh38.p7 | 8:55889510 | accacacccagccCA[A/T]GTATATTTATCGAGT | 4067 |
rs867586 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | LYN | GRCh38.p7 | 8:55984760 | ACTCTCAGCCCTCCA[A/G]TTCTTCTTGGCTTCA | 4067 |
rs868541 | snp | A/G | 0.481396 | 0.0946345 | intron-variant | LYN | GRCh38.p7 | 8:55964201 | AAAAATGCAGTACAA[A/G]ATAAGTGTTAGAACA | 4067 |
rs907422 | snp | A/C | 0.0707826 | 0.174302 | intron-variant | LYN | GRCh38.p7 | 8:55971324 | CCAACCCCACCTATT[A/C]CTCTTACTGCAGAGA | 4067 |
rs907423 | snp | C/G | 0.460589 | 0.13473 | intron-variant | LYN | GRCh38.p7 | 8:55971059 | GAGGATGCCTGAGCA[C/G]TGTGACTCACCCATC | 4067 |
rs907424 | snp | A/G | 0.482234 | 0.0925596 | intron-variant | LYN | GRCh38.p7 | 8:55963660 | TGCATTTCTCTGGTT[A/G]CTAATAAGATTGAGT | 4067 |
rs907425 | snp | C/T | 0.491104 | 0.0660973 | intron-variant | LYN | GRCh38.p7 | 8:55963732 | AAATGCCCTTCCAAG[C/T]CTTTGCCTATTTCTT | 4067 |
rs925448 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYN | GRCh38.p7 | 8:56006776 | AAGCAGATCACCAGC[C/T]AATGGGTGTTTACTT | 4067 |
rs952784 | snp | A/G | 0.319616 | 0.240112 | intron-variant | LYN | GRCh38.p7 | 8:55971530 | GGGCTATGGAACATC[A/G]GGACACATGGCCTGG | 4067 |
rs1027985 | snp | C/G | 0.461813 | 0.132798 | intron-variant | LYN | GRCh38.p7 | 8:55970612 | TGAGGGAAGAAGTGG[C/G]AGTGAAAAAGGAAGA | 4067 |
rs1027986 | snp | C/T | 0.460589 | 0.13473 | intron-variant | LYN | GRCh38.p7 | 8:55969912 | TCTTTTTCTCATAAC[C/T]GCTGCTGGGAAACAT | 4067 |
rs1027987 | snp | C/T | 0.460589 | 0.13473 | intron-variant | LYN | GRCh38.p7 | 8:55969624 | CTATTACAGGGGAAC[C/T]CCCCACAAAATGATT | 4067 |
rs1027989 | snp | C/G | 0.164873 | 0.23506 | intron-variant | LYN | GRCh38.p7 | 8:55901862 | CTGAAAGTCATTTTT[C/G]ATTTAGGTTCTTCCC | 4067 |
rs1027990 | snp | C/T | 0.445987 | 0.155207 | intron-variant | LYN | GRCh38.p7 | 8:55901750 | ACATCCAGCTCCGCG[C/T]TGGAAATATCTGAAG | 4067 |
rs1050855 | snp | A/G | 0.497933 | 0.0320782 | utr-variant-5-prime, missense | LYN | GRCh38.p7 | 8:55880027 | CGCAGGTCCTGCTGG[A/G]CCGCCCCGTCGCGCC | 4067 |
rs1050875 | snp | A/C/T | 1.64798e-05 | 0.00287047 | synonymous-codon | LYN | GRCh38.p7 | 8:55998432 | GGTCTCCGAGTCACT[A/C/T]ATGTGCAAAATTGCA | 4067 |
rs1123750 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | LYN | GRCh38.p7 | 8:55926951 | AGATTCAGATAAATT[A/G]GGCAGAAATTACAGA | 4067 |
rs1124745 | snp | A/G | 0.0955749 | 0.196603 | intron-variant | LYN | GRCh38.p7 | 8:55901611 | TTGCTCTGTGGGGTC[A/G]GGTAGGGCCGGGGGA | 4067 |
rs1126327 | snp | C/T | 0.147991 | 0.228242 | intron-variant | LYN | GRCh38.p7 | 8:55938860 | CTGTGTGAGTGAGTC[C/T]TAGCCTCACCCCTCC | 4067 |
rs1397974 | snp | C/T | 0.493793 | 0.055364 | intron-variant | LYN | GRCh38.p7 | 8:55886552 | TGTGGTCAAATAAGT[C/T]TGACAggctgggcgc | 4067 |
rs1397975 | snp | G/T | 0.165853 | 0.235413 | intron-variant | LYN | GRCh38.p7 | 8:55912838 | AGTCCATTAAAAGAA[G/T]ACATATTTTTAATCA | 4067 |
rs1397976 | snp | A/G | 0.422158 | 0.181278 | intron-variant | LYN | GRCh38.p7 | 8:55912826 | GAATACATATTTTTA[A/G]TCAGGAAATATAATA | 4067 |
rs1450738 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | LYN | GRCh38.p7 | 8:55882538 | ACATTGTTATAAGCT[C/T]ACTCCTACTGATGAT | 4067 |
rs1450739 | snp | C/T | 0.297382 | 0.245469 | intron-variant | LYN | GRCh38.p7 | 8:55882672 | ACTGGCTCTTCCTAG[C/T]GATGATGGTGAAGGT | 4067 |
rs1450740 | snp | A/C | 0.133093 | 0.220981 | upstream-variant-2KB, utr-variant-5-prime | LYN | GRCh38.p7 | 8:55877987 | CCAGTAGTTGAGGAG[A/C]CAAGCCTAACATGGG | 4067 |
rs1450741 | snp | C/T | 0.406986 | 0.194565 | upstream-variant-2KB, missense | LYN | GRCh38.p7 | 8:55879600 | AAGCCCAGGCTCCTC[C/T]GGAGATCCTTCCGTC | 4067 |
rs1466138 | snp | A/C | 0.182933 | 0.240836 | intron-variant | LYN | GRCh38.p7 | 8:55895382 | ATCCATACCTATATT[A/C]TTCACCAAGATTAGT | 4067 |
rs1470707 | snp | C/T | 0.421842 | 0.181577 | intron-variant | LYN | GRCh38.p7 | 8:55903935 | TGAGATGGGAGGATC[C/T]GCTTGAGCCTCGGAG | 4067 |
rs1470708 | snp | A/G | 0.499897 | 0.00718776 | intron-variant | LYN | GRCh38.p7 | 8:55904151 | AAAAAAAATAATAGC[A/G]GGACTTTAATAGATA | 4067 |
rs1473075 | snp | C/G/T | 0.0498117 | 0.149749 | intron-variant | LYN | GRCh38.p7 | 8:55941113 | CCCTACCTATGTTTA[C/G/T]CTGGAGCCAGGTTCT | 4067 |
rs1511723 | snp | C/T | 0.17461 | 0.238362 | intron-variant | LYN | GRCh38.p7 | 8:55890620 | acacaagtgtacaaa[C/T]atctctgagacccca | 4067 |
rs1511724 | snp | C/G | 0.499824 | 0.00938333 | intron-variant | LYN | GRCh38.p7 | 8:55884138 | CACTCCAGGCTGGGC[C/G]ACAGAGTGAGCCTTC | 4067 |
rs1546518 | snp | C/G | 0.422 | 0.181428 | intron-variant | LYN | GRCh38.p7 | 8:55912335 | CTAGGAGTATTCAAG[C/G]CTGATTTCTTTCCTT | 4067 |
rs1546519 | snp | C/T | 0.283158 | 0.247791 | intron-variant | LYN | GRCh38.p7 | 8:55911999 | AAGGGCTAGAAGGGA[C/T]GTGGTAGAACACACC | 4067 |
rs1562818 | snp | C/T | 0.163892 | 0.234703 | intron-variant | LYN | GRCh38.p7 | 8:55891915 | TCAGCCAGCAATCCA[C/T]GTGGCCATGTATTAA | 4067 |
rs1828527 | snp | C/T | 0.16618 | 0.23553 | intron-variant | LYN | GRCh38.p7 | 8:55912542 | TACGGGGTTTCGCCA[C/T]GTTGGCCAGGCTGGT | 4067 |
rs1849195 | snp | A/G | | | intron-variant | LYN | GRCh38.p7 | 8:55930828 | CATCAGCTCATCCCA[A/G]GACCTTGGCAGGGCC | 4067 |
rs1877301 | snp | A/T | 0.463881 | 0.12944 | intron-variant | LYN | GRCh38.p7 | 8:55964031 | ACAATAACTCTTAAG[A/T]TCTACAGAAAAGGCC | 4067 |
rs1912818 | snp | G/T | 0.336474 | 0.234568 | intron-variant | LYN | GRCh38.p7 | 8:55991762 | TGGTGCACCCCCACA[G/T]GCTCCCTTGTCCCTG | 4067 |
rs1963650 | snp | A/G | 0.474453 | 0.110094 | intron-variant | LYN | GRCh38.p7 | 8:55902250 | gaggcaaaaatgggc[A/G]gatcacctgaggttg | 4067 |
rs1973610 | snp | C/T | 0.474272 | 0.110462 | intron-variant | LYN | GRCh38.p7 | 8:55902236 | cagatcacctgaggt[C/T]gggagttcgagacca | 4067 |
rs1979128 | snp | A/G | 0.473174 | 0.112665 | intron-variant | LYN | GRCh38.p7 | 8:55901451 | TCAAGGCCAGGCTTT[A/G]GACTCCTTCTTGGGC | 4067 |
rs1980041 | snp | A/G | 0.445064 | 0.156365 | intron-variant | LYN | GRCh38.p7 | 8:55900446 | GTTCAAGGCTGCAGA[A/G]AGCAATGATCACATC | 4067 |
rs1980042 | snp | C/T | 0.474 | 0.111014 | intron-variant | LYN | GRCh38.p7 | 8:55900083 | TTGTCTTCCTGAAGT[C/T]CGAGTGGCAGCGCAT | 4067 |
rs1995976 | snp | A/G | 0.343701 | 0.231776 | intron-variant | LYN | GRCh38.p7 | 8:56009508 | gtgctagccaggttg[A/G]tttctcctgaggcct | 4067 |
rs2012149 | snp | C/T | 0.149999 | 0.229128 | intron-variant | LYN | GRCh38.p7 | 8:55902516 | GTGTACTTTGTACAA[C/T]TCAACTTctagaaaa | 4067 |
rs2036897 | snp | A/G | 0.455383 | 0.142541 | intron-variant | LYN | GRCh38.p7 | 8:55972576 | AGGAGGAGGAGGAGC[A/G]CTGGGTAGCAGTGGT | 4067 |
rs2036898 | snp | C/G | 0.205723 | 0.246048 | intron-variant | LYN | GRCh38.p7 | 8:55972539 | TGAGGGCATCCCAGG[C/G]GGACGAGGGAGCAGG | 4067 |
rs2100245 | snp | C/T | 0.380724 | 0.213099 | intron-variant | LYN | GRCh38.p7 | 8:55937541 | CACTGCACAGGGGCA[C/T]AAGGATGTTCCCGCT | 4067 |
rs2137126 | snp | A/C | 0.497881 | 0.0324789 | intron-variant | LYN | GRCh38.p7 | 8:55898968 | gcacagtggtgtaca[A/C]ctgtggtcccagcta | 4067 |
rs2175487 | snp | C/T | 0.206947 | 0.246265 | intron-variant | LYN | GRCh38.p7 | 8:55999302 | GCGGAGTTTCACTCT[C/T]GTCACCCAGGCTGGA | 4067 |
rs2227978 | snp | C/T | 0.018945 | 0.0954651 | synonymous-codon | LYN | GRCh38.p7 | 8:55998369 | GGGAATGGCATACAT[C/T]GAGCGGAAGAACTAC | 4067 |
rs2227979 | snp | C/T | 0.00872672 | 0.0654768 | synonymous-codon | LYN | GRCh38.p7 | 8:55953956 | GGTGAAAAGGCTTGG[C/T]GCTGGGCAGTTTGGG | 4067 |
rs2227980 | snp | A/G | 0.114597 | 0.210157 | synonymous-codon | LYN | GRCh38.p7 | 8:55953893 | TCCCAAGCCACAGAA[A/G]CCATGGGATAAAGAT | 4067 |
rs2271400 | snp | A/G | 0.416218 | 0.186739 | upstream-variant-2KB, utr-variant-5-prime | LYN | GRCh38.p7 | 8:55878685 | GAGAAGGGGTGGGTT[A/G]CCCATGGAAATACCC | 4067 |
rs2292419 | snp | C/T | 0.301932 | 0.244547 | intron-variant | LYN | GRCh38.p7 | 8:55954221 | TAAGGAGGGGAGTAA[C/T]GGGTATTTATCTTGA | 4067 |
rs2317199 | snp | C/T | | | intron-variant | LYN | GRCh38.p7 | 8:55973126 | ATCTGTATCTGGCCT[C/T]TTCTTCCCGCTCCCC | 4067 |
rs2317200 | snp | C/T | | | intron-variant | LYN | GRCh38.p7 | 8:55973129 | TGTATCTGGCCTCTT[C/T]TTCCCGCTCCCCACT | 4067 |
rs2443049 | snp | A/G | | | intron-variant | LYN | GRCh38.p7 | 8:55909012 | tgtgtgtgtgtgtgt[A/G]tatatatatatatat | 4067 |
rs2458083 | snp | A/G | 0.15698 | 0.23205 | intron-variant | LYN | GRCh38.p7 | 8:55986226 | TTATGTATATGCTAA[A/G]GGAGTAGTCATGGCA | 4067 |
rs2466007 | snp | A/G | 0.488118 | 0.0761554 | intron-variant | LYN | GRCh38.p7 | 8:55976628 | TAGCATGCGGTGCCC[A/G]CTCTGACAGCCCTTG | 4067 |
rs2667971 | snp | A/G | 0.394904 | 0.203722 | intron-variant | LYN | GRCh38.p7 | 8:55994601 | GCCACACAGGTGGGC[A/G]TGATGGCAGGGACCC | 4067 |
rs2667972 | snp | A/G | 0.157311 | 0.232183 | intron-variant | LYN | GRCh38.p7 | 8:55994102 | TGGTCTATTTACTAC[A/G]GCTAAGTAAATCCAG | 4067 |
rs2667973 | snp | G/T | 0.336474 | 0.234568 | intron-variant | LYN | GRCh38.p7 | 8:55994031 | GCTGATTGAATGTAG[G/T]GTCAACTTTTCATGG | 4067 |
rs2667974 | snp | G/T | 0.336474 | 0.234568 | intron-variant | LYN | GRCh38.p7 | 8:55992818 | AGTTTGACCCTTTTT[G/T]TGCCCTTCCACCTTC | 4067 |
rs2667975 | snp | A/G | 0.336474 | 0.234568 | intron-variant | LYN | GRCh38.p7 | 8:55992571 | TTGGGGAGGAAGTCC[A/G]GATGCAACTCAGCTT | 4067 |
rs2667976 | snp | G/T | 0.336474 | 0.234568 | intron-variant | LYN | GRCh38.p7 | 8:55992164 | AATGTCAGGCCCAGG[G/T]GTGAACAAAGACAAG | 4067 |
rs2667977 | snp | C/T | 0.336474 | 0.234568 | intron-variant | LYN | GRCh38.p7 | 8:55991685 | GCCTGTGCCTGAAGC[C/T]GATGACAAAGAAGAC | 4067 |
rs2667978 | snp | C/T | 0.210909 | 0.246925 | intron-variant | LYN | GRCh38.p7 | 8:55985392 | TCAAAATACCATGTG[C/T]TTGCGAGGGAAGCCT | 4067 |
rs2667979 | snp | C/T | 0.373598 | 0.21731 | intron-variant | LYN | GRCh38.p7 | 8:55985242 | GCTCACCAGGTAGGA[C/T]TTGTCCATGCCTAGT | 4067 |
rs2667980 | snp | A/T | 0.15665 | 0.231917 | intron-variant | LYN | GRCh38.p7 | 8:55983982 | AGAGGTACGGAAGGA[A/T]TCTTCCCAAGAACCT | 4067 |
rs2667981 | snp | A/T | 0.157311 | 0.232183 | intron-variant | LYN | GRCh38.p7 | 8:55981744 | CAGGAAAGTAAACCT[A/T]TAGTTAGAGGAAGGG | 4067 |
rs2667982 | snp | A/C | 0.398534 | 0.201091 | intron-variant | LYN | GRCh38.p7 | 8:55981608 | AGCACTTTGGGAGGC[A/C]GAGGTGGGAGGACTG | 4067 |
rs2667983 | snp | A/C | 0.156319 | 0.231784 | intron-variant | LYN | GRCh38.p7 | 8:55981528 | TCTCTATATTAAAAA[A/C]AATTTTTTTAAACAC | 4067 |
rs2667984 | snp | A/G | 0.25045 | 0.25 | intron-variant | LYN | GRCh38.p7 | 8:55973851 | TCAAGCAATCCTCCC[A/G]TTTCAGCCTCCCAAG | 4067 |
rs2667985 | snp | C/G | 0.140242 | 0.224618 | intron-variant | LYN | GRCh38.p7 | 8:55967799 | TTGATTCAAAGTCTT[C/G]TATATGAAGGTGATC | 4067 |
rs2667986 | snp | C/T | 0.156319 | 0.231784 | intron-variant | LYN | GRCh38.p7 | 8:55967462 | ctgggcatggtggca[C/T]gtgcctgtagtccca | 4067 |
rs2667987 | snp | A/G | 0.254105 | 0.249966 | intron-variant | LYN | GRCh38.p7 | 8:55967406 | aatcgcttgaacccg[A/G]gaggcaggggttgca | 4067 |
rs2667988 | snp | C/G | 0.48155 | 0.0942576 | intron-variant | LYN | GRCh38.p7 | 8:55966554 | ACAGTGAAACCCCAT[C/G]TCTACTAAAAATACA | 4067 |
rs2667989 | snp | A/G | 0.258288 | 0.249863 | intron-variant | LYN | GRCh38.p7 | 8:55966384 | TGCGACTCCGTCTCA[A/G]TTAAAAAAAAAAAAA | 4067 |
rs2667990 | snp | C/G | 0.373196 | 0.217538 | intron-variant | LYN | GRCh38.p7 | 8:56000661 | ggctcactgcaacct[C/G]tgcttcccaggttga | 4067 |
rs2668010 | snp | C/T | 0.373397 | 0.217424 | intron-variant | LYN | GRCh38.p7 | 8:56007884 | AGCACTTTGGGAGGC[C/T]GAGACAGGCAGACGA | 4067 |
rs2668011 | snp | C/T | 0.256897 | 0.249905 | utr-variant-3-prime | LYN | GRCh38.p7 | 8:56011499 | TGCTTTAAACTTGCC[C/T]AAGTTCTACCTCCTT | 4067 |
rs2668015 | snp | A/G | 0.417845 | 0.185278 | intron-variant | LYN | GRCh38.p7 | 8:55956896 | AGAAGACAGGAGGAA[A/G]GGAGAAAAGAGTGTA | 4067 |
rs2668016 | snp | C/T | 0.306927 | 0.243432 | intron-variant | LYN | GRCh38.p7 | 8:55957046 | CAGATAAGCAACTTA[C/T]TCAAGGTCATTCAAG | 4067 |
rs2668017 | snp | C/T | 0.307176 | 0.243374 | intron-variant | LYN | GRCh38.p7 | 8:55957307 | TCTAGTTATTGGAAG[C/T]TATATTTTGGTGTAT | 4067 |
rs2668018 | snp | C/T | 0.424348 | 0.179172 | intron-variant | LYN | GRCh38.p7 | 8:55959543 | GCAAAGGCTATACAG[C/T]AGAGGAAAGAAATTG | 4067 |
rs2668019 | snp | C/G | 0.418169 | 0.184985 | intron-variant | LYN | GRCh38.p7 | 8:55959748 | aaagtacaaacaact[C/G]aaatgtccatcagat | 4067 |
rs2668020 | snp | A/G | 0.418007 | 0.185132 | intron-variant | LYN | GRCh38.p7 | 8:55959992 | agaaagtagatgact[A/G]gttgcctagggctgg | 4067 |
rs2668021 | snp | C/T | 0.334412 | 0.235318 | intron-variant | LYN | GRCh38.p7 | 8:55960988 | GAATCAACTGGGCAG[C/T]GAGGCTAAGGACGAT | 4067 |
rs2668022 | snp | A/G | 0.257732 | 0.24988 | intron-variant | LYN | GRCh38.p7 | 8:55964492 | CTGCTAGCTATAAAT[A/G]AACTTTTTATTATTT | 4067 |
rs2719229 | snp | C/T | 0.480539 | 0.0967035 | intron-variant | LYN | GRCh38.p7 | 8:55975561 | ATATATTTGTGTTCC[C/T]TTATTTAGAGCAATG | 4067 |
rs2719230 | snp | C/T | 0.263809 | 0.249618 | intron-variant | LYN | GRCh38.p7 | 8:55975519 | TATCAATGTCATCTG[C/T]ATAGCCTCAGAATCA | 4067 |
rs2719231 | snp | C/T | 0.474363 | 0.110278 | intron-variant | LYN | GRCh38.p7 | 8:55974104 | GGCCAAGTCCAAGTT[C/T]ACCTCGTTATCTGTA | 4067 |
rs2719232 | snp | C/T | 0.480382 | 0.097079 | intron-variant | LYN | GRCh38.p7 | 8:55973625 | AAATTTTTCACTGCT[C/T]TTTCCTCTCAGTTTG | 4067 |
rs2719233 | snp | C/T | 0.155325 | 0.23138 | intron-variant | LYN | GRCh38.p7 | 8:55973597 | TTGACATGTCTATGA[C/T]TCCATCTCAGCTTCT | 4067 |
rs2719234 | snp | G/T | 0.46875 | 0.121031 | intron-variant | LYN | GRCh38.p7 | 8:55967332 | TTTTTTTTTTTTTTT[G/T]GAAACAGAGTCTCAC | 4067 |
rs2719235 | snp | G/T | 0.372995 | 0.217652 | utr-variant-3-prime, downstream-variant-500B | LYN | GRCh38.p7 | 8:56011790 | TGCCATGTTCAGAAC[G/T]ATAGAATATTACTGT | 4067 |
rs2719236 | snp | C/T | 0.372391 | 0.217992 | utr-variant-3-prime, downstream-variant-500B | LYN | GRCh38.p7 | 8:56011803 | ACTATAGAATATTAC[C/T]GTTACATAATGTCTG | 4067 |
rs2719240 | snp | C/G | 0.418491 | 0.184691 | intron-variant | LYN | GRCh38.p7 | 8:55957489 | AAGATTCCAAGCCAT[C/G]ACTTTATATGCAGGG | 4067 |
rs2719241 | snp | C/T | 0.291102 | 0.248845 | intron-variant | LYN | GRCh38.p7 | 8:55957251 | TAAAAATAGGGCACA[C/T]GGAGTCAGACTCTGG | 4067 |
rs2719242 | snp | A/G | 0.372995 | 0.217652 | intron-variant | LYN | GRCh38.p7 | 8:55994673 | ATTGGGCCTGAAACC[A/G]CAGTTGACAATAGCA | 4067 |
rs2719243 | snp | A/G | 0.336474 | 0.234568 | intron-variant | LYN | GRCh38.p7 | 8:55994417 | ACAGACTTGCAACAA[A/G]CCTAGTGTATTTTGG | 4067 |
rs2719244 | snp | A/G | 0.25634 | 0.24992 | intron-variant | LYN | GRCh38.p7 | 8:55971022 | CTTTACTGGAAGGAT[A/G]GGCATTGCCCTCCCT | 4067 |
rs2719245 | snp | C/G | 0.157311 | 0.232183 | intron-variant | LYN | GRCh38.p7 | 8:55981800 | ATAAAAGTGAGAAAA[C/G]AAGAAGGAAGTAGAA | 4067 |
rs2719246 | snp | G/T | 0.114738 | 0.210248 | intron-variant | LYN | GRCh38.p7 | 8:55981862 | GTGCAGCTTTGTTTT[G/T]CATTCCTTGTGGCAT | 4067 |
rs2719247 | snp | C/T | | | intron-variant | LYN | GRCh38.p7 | 8:56000725 | agagtgagactctgt[C/T]tcaaaaaaaaaaaaa | 4067 |
rs2719248 | snp | A/T | 0.373196 | 0.217538 | intron-variant | LYN | GRCh38.p7 | 8:56000968 | GGGGAGAGACTGATG[A/T]TTATCAAACACACAG | 4067 |
rs2719251 | snp | A/G | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55992134 | TCGGCAGGTGGTTTA[A/G]AAAGTTGGGGTTTTC | 4067 |
rs2719252 | snp | C/T | 0.336474 | 0.234568 | intron-variant | LYN | GRCh38.p7 | 8:55992293 | CTCTGGGCCCAGAGC[C/T]GTGATAGAGAGGGAG | 4067 |
rs2719253 | snp | C/T | 0.336474 | 0.234568 | intron-variant | LYN | GRCh38.p7 | 8:55992607 | ATGATGGTAACAGTC[C/T]ACCTGTGAGGTTGCT | 4067 |
rs2719254 | snp | G/T | 0.480302 | 0.0972668 | intron-variant | LYN | GRCh38.p7 | 8:55969039 | taatcccagcccttt[G/T]ggaggccaaggtggg | 4067 |
rs2719265 | snp | C/T | 0.463881 | 0.12944 | intron-variant | LYN | GRCh38.p7 | 8:55962718 | GGACTAACATGAACT[C/T]CAATTTCATCAGTAA | 4067 |
rs2719266 | snp | C/T | 0.463451 | 0.130149 | intron-variant | LYN | GRCh38.p7 | 8:55962144 | ATCTTACCaacacca[C/T]atggaatgaagatga | 4067 |
rs2719267 | snp | A/G | 0.458315 | 0.13822 | intron-variant | LYN | GRCh38.p7 | 8:55961458 | ATATTGAAACAATAG[A/G]GTGGTTTTCATCCCT | 4067 |
rs2719268 | snp | A/G | 0.289424 | 0.246872 | intron-variant | LYN | GRCh38.p7 | 8:55959523 | ATAGCCTTTGCACTA[A/G]TGTGACATATTTTCT | 4067 |
rs2873327 | snp | G/T | | | intron-variant | LYN | GRCh38.p7 | 8:55932429 | tttGTTTGTTTGTTT[G/T]TGTTTTTTTTT | 4067 |
rs2873328 | snp | G/T | | | intron-variant | LYN | GRCh38.p7 | 8:55932435 | TGTTTGTTTTTGTTT[G/T]TTTTT | 4067 |
rs3106348 | snp | C/T | 0.361474 | 0.223771 | intron-variant | LYN | GRCh38.p7 | 8:56004607 | ccACAAAAAGACTTC[C/T]AATGAAAAATTCCCC | 4067 |
rs3735904 | snp | A/G | 0.0111196 | 0.0737302 | utr-variant-3-prime, downstream-variant-500B | LYN | GRCh38.p7 | 8:56011860 | AAGGTTTTTGTGTAC[A/G]CCCCCCTGCTTGCAT | 4067 |
rs3808391 | snp | C/T | 0.4944 | 0.0526182 | upstream-variant-2KB, utr-variant-5-prime | LYN | GRCh38.p7 | 8:55878090 | TATTTAAAGCTCCTA[C/T]TGATAGGCAACTTTT | 4067 |
rs3930177 | snp | G/T | | | intron-variant | LYN | GRCh38.p7 | 8:55932431 | tgtttgtttgttttt[G/T]ttttttttt | 4067 |
rs3968371 | snp | A/G | 0.39214 | 0.205661 | intron-variant | LYN | GRCh38.p7 | 8:55937576 | TAAAGAACAAATTTC[A/G]AGAAGTGGAATTCCA | 4067 |
rs4061077 | snp | A/G | 0.337614 | 0.234145 | intron-variant | LYN | GRCh38.p7 | 8:55990883 | aattttgttttacaT[A/G]TTTTAAACCTCATAC | 4067 |
rs4130542 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | LYN | GRCh38.p7 | 8:55971357 | AAATG[A/G] | 4067 |
rs4434595 | snp | A/G | 0.394354 | 0.204112 | intron-variant | LYN | GRCh38.p7 | 8:55910610 | tgctccttctggaca[A/G]gattgctttggtatt | 4067 |
rs4436100 | snp | C/T | 0.394354 | 0.204112 | intron-variant | LYN | GRCh38.p7 | 8:55910849 | tgtggcacctctgct[C/T]tttgtagttttcgta | 4067 |
rs4449764 | snp | A/G | 0.445987 | 0.155207 | intron-variant | LYN | GRCh38.p7 | 8:55913005 | ATGATGCTACTTATT[A/G]AAAATGACAAGTGAT | 4067 |
rs4551325 | snp | C/T | 0.394354 | 0.204112 | intron-variant | LYN | GRCh38.p7 | 8:55910632 | tttggtatttgtgct[C/T]tcttttggttccata | 4067 |
rs4593518 | snp | A/G | 0.374 | 0.217081 | intron-variant | LYN | GRCh38.p7 | 8:56004387 | caacctccacctccc[A/G]ggttcaagcaatgct | 4067 |
rs4737419 | snp | C/T | 0.499368 | 0.0177603 | intron-variant | LYN | GRCh38.p7 | 8:55885898 | ATGCTGCGTTTTCCT[C/T]GGGGTTCTTTCTACC | 4067 |
rs4737420 | snp | C/T | 0.49334 | 0.057322 | intron-variant | LYN | GRCh38.p7 | 8:55895622 | TAGTGAGACCTCATC[C/T]CTACAATTTTTTTTT | 4067 |
rs4737421 | snp | A/T | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55931621 | CCTCACAAAATGATA[A/T]CATGCTATATATACT | 4067 |
rs4738464 | snp | C/T | 0.487368 | 0.0784625 | intron-variant | LYN | GRCh38.p7 | 8:55902093 | GCTTACCACAACCTC[C/T]GTCTCCTGGGTTCAA | 4067 |
rs4738466 | snp | A/G | 0.179425 | 0.239831 | intron-variant | LYN | GRCh38.p7 | 8:55998142 | TTTAAGATGACCATT[A/G]TTGGAGATTTGGCAG | 4067 |
rs5891598 | in-del | -/T | | | intron-variant | LYN | GRCh38.p7 | 8:55900540 | ACCATGCCCAGCTAA[-/T]TTTTTTTTTTTTTTT | 4067 |
rs5891599 | in-del | -/A/AA/AAAA/AAAAA/AAAT | 0.310357 | 0.281016 | intron-variant | LYN | GRCh38.p7 | 8:55904006 | GTAAGACAGAGTCTC[-/A/AA/AAAA/AAAAA/AAAT]AAAAAAAAAGTGTTT | 4067 |
rs5891600 | in-del | -/C | 0.184203 | 0.241186 | intron-variant | LYN | GRCh38.p7 | 8:55912738 | TCTGAAAAAAAAAAA[-/C]AAAACAAAACAAAAC | 4067 |
rs6474025 | snp | C/T | 0.021333 | 0.101051 | upstream-variant-2KB | LYN | GRCh38.p7 | 8:55876678 | AGTTAGGTCTGTGGC[C/T]AAGTTGGCAAGAGTT | 4067 |
rs6474026 | snp | C/T | 0.296109 | 0.245711 | intron-variant | LYN | GRCh38.p7 | 8:55880934 | GATTAGCGGTTGTGT[C/T]TTTGTATATCCGAGT | 4067 |
rs6474027 | snp | G/T | 0.109461 | 0.206758 | intron-variant | LYN | GRCh38.p7 | 8:55904103 | TGTTCTCTGAAAGTT[G/T]ATAAACAATGAGGTA | 4067 |
rs6474028 | snp | A/G | 0.170733 | 0.237101 | intron-variant | LYN | GRCh38.p7 | 8:55904489 | TGGGGTTAGGTTGGC[A/G]GTGGATAAATTCCAG | 4067 |
rs6474029 | snp | A/G | 0.153997 | 0.230832 | intron-variant | LYN | GRCh38.p7 | 8:55904547 | TATGATGCCACACAA[A/G]ATAATTTCTGTATGT | 4067 |
rs6474030 | snp | C/G | 0.153997 | 0.230832 | intron-variant | LYN | GRCh38.p7 | 8:55905589 | ACCGCAAGGTCATCT[C/G]GGGAAAAGGGAACCA | 4067 |
rs6474031 | snp | C/T | 0.389152 | 0.207694 | intron-variant | LYN | GRCh38.p7 | 8:55908330 | actcactgcaacctc[C/T]gcctcccaggttcga | 4067 |
rs6474032 | snp | A/C | 0.389152 | 0.207694 | intron-variant | LYN | GRCh38.p7 | 8:55908425 | aatttttgtattttt[A/C]gtagagacagggttt | 4067 |
rs6474033 | snp | A/G | 0.162581 | 0.234218 | intron-variant | LYN | GRCh38.p7 | 8:55913457 | GTCATTCTTGGGACT[A/G]GCAAATCTAGAAAAC | 4067 |
rs6474036 | snp | C/T | 0.206029 | 0.246103 | intron-variant | LYN | GRCh38.p7 | 8:55995391 | GACACGAAGTCACTG[C/T]TCTCCAAACCTGCCC | 4067 |
rs6982669 | snp | A/G | 0.394354 | 0.204112 | intron-variant | LYN | GRCh38.p7 | 8:55910486 | attcctgggttctct[A/G]ttctgtcccattgat | 4067 |
rs6983130 | snp | A/G | 0.296364 | 0.245663 | intron-variant | LYN | GRCh38.p7 | 8:55880680 | ACGTCGAGGGGCTGC[A/G]GCGGAGGCTGGAACT | 4067 |
rs6984608 | snp | G/T | 0.0524604 | 0.153226 | intron-variant | LYN | GRCh38.p7 | 8:55915122 | TTATCTATTATCTGC[G/T]CTTTCTTTTGAAAAT | 4067 |
rs6985030 | snp | A/G | 0.24449 | 0.249939 | intron-variant | LYN | GRCh38.p7 | 8:55932317 | CTACTAATTACTAGT[A/G]ACAGATTAATATAGT | 4067 |
rs6985298 | snp | A/G/T | 0.0520825 | 0.152737 | utr-variant-3-prime | LYN | GRCh38.p7 | 8:56010658 | CCAGATTTCAATGAT[A/G/T]TTTTTCCCCCTACCT | 4067 |
rs6986187 | snp | A/T | 0.394354 | 0.204112 | intron-variant | LYN | GRCh38.p7 | 8:55910171 | tctcatttgtctact[A/T]ttgtttttgttgcct | 4067 |
rs6986193 | snp | G/T | 0.394354 | 0.204112 | intron-variant | LYN | GRCh38.p7 | 8:55910172 | ctcatttgtctactt[G/T]tgtttttgttgcctg | 4067 |
rs6986361 | snp | A/G | 0.483636 | 0.0889627 | intron-variant | LYN | GRCh38.p7 | 8:55886304 | GTAGTACAATGGTGC[A/G]ATCTCCACTCACTGC | 4067 |
rs6988731 | snp | A/T | 0.206029 | 0.246103 | intron-variant | LYN | GRCh38.p7 | 8:55986299 | cattcctgccagcag[A/T]gtgtgagatttccag | 4067 |
rs6988900 | snp | G/T | 0.0513262 | 0.151752 | intron-variant | LYN | GRCh38.p7 | 8:55956319 | ttgaccacctgagat[G/T]aagtgcagacgtgaC | 4067 |
rs6989378 | snp | C/T | 0.493247 | 0.0577133 | intron-variant | LYN | GRCh38.p7 | 8:55892947 | CAAGCAGTACTCCCC[C/T]GAAAGGCATCTGCCA | 4067 |
rs6990948 | snp | A/G | 0.030278 | 0.119257 | intron-variant | LYN | GRCh38.p7 | 8:55991447 | TTCTTCTCATTGTAT[A/G]TTACAAAGGCCACTC | 4067 |
rs6991715 | snp | A/G | 0.299916 | 0.244966 | intron-variant | LYN | GRCh38.p7 | 8:55917414 | gtcttgaacttttgg[A/G]ctaaactgatcctcc | 4067 |
rs6993642 | snp | C/T | 0.165853 | 0.235413 | intron-variant | LYN | GRCh38.p7 | 8:55891300 | gaggttgcagtgagt[C/T]gagatcccgcgactg | 4067 |
rs6994798 | snp | A/T | 0.095934 | 0.196885 | intron-variant | LYN | GRCh38.p7 | 8:55900127 | GAAAACCAGTCAGCA[A/T]GGCCAAAACAAGAGA | 4067 |
rs6995146 | snp | A/C/G | 0.095934 | 0.196885 | intron-variant | LYN | GRCh38.p7 | 8:55900359 | GTTGGGGGAAAAATA[A/C/G]TCTTCCTCtttttta | 4067 |
rs6995519 | snp | A/T | 0.179744 | 0.239925 | intron-variant | LYN | GRCh38.p7 | 8:55917286 | gaactcctaggctca[A/T]gtgatcgtcccgcct | 4067 |
rs6996664 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | LYN | GRCh38.p7 | 8:55962514 | GGCTATGGTTCATTC[A/G]TCTTCATCCCATGTC | 4067 |
rs6997193 | snp | A/G | 0.498908 | 0.0233371 | intron-variant | LYN | GRCh38.p7 | 8:55897890 | TGTACTCCAGCCTGC[A/G]TGACAGTGAGGCCCT | 4067 |
rs6999117 | snp | A/G | 0.178465 | 0.239547 | intron-variant | LYN | GRCh38.p7 | 8:55883591 | AAGTACCTGAGTAAT[A/G]CTTTGCAAAAGGACT | 4067 |
rs6999495 | snp | A/G | 0.153997 | 0.230832 | intron-variant | LYN | GRCh38.p7 | 8:55906609 | taatccacctgtctc[A/G]gcctcccaaagtact | 4067 |
rs7000094 | snp | C/T | 0.444799 | 0.156695 | intron-variant | LYN | GRCh38.p7 | 8:55900800 | TTTGCTAAATACTTA[C/T]CTAGCTTGCATTTTT | 4067 |
rs7001010 | snp | C/T | 0.394354 | 0.204112 | intron-variant | LYN | GRCh38.p7 | 8:55910359 | ccagtttcattcttc[C/T]gcatatggcaaccag | 4067 |
rs7001196 | snp | C/T | 0.394354 | 0.204112 | intron-variant | LYN | GRCh38.p7 | 8:55910474 | atttatagctttatt[C/T]ctgggttctctattc | 4067 |
rs7002800 | snp | C/T | 0.242775 | 0.249896 | intron-variant | LYN | GRCh38.p7 | 8:55898265 | tgatcgttttattgt[C/T]ttttataataacaGC | 4067 |
rs7002888 | snp | C/G | 0.448963 | 0.151372 | intron-variant | LYN | GRCh38.p7 | 8:55956082 | gcctctgttgaattt[C/G]aagaaccacaaaact | 4067 |
rs7003678 | snp | C/T | | | intron-variant | LYN | GRCh38.p7 | 8:55956525 | TAAATTTAGTTTCTC[C/T]GTGGCAACTTTTTAC | 4067 |
rs7003770 | snp | C/T | 0.296109 | 0.245711 | intron-variant | LYN | GRCh38.p7 | 8:55906776 | AATAAATGAAATGTA[C/T]CCCAGTTGAACAACA | 4067 |
rs7004280 | snp | C/G | 0.113685 | 0.209567 | intron-variant | LYN | GRCh38.p7 | 8:55981791 | TTGGTTGAAATAAAA[C/G]TGAGAAAAGAAGAAG | 4067 |
rs7004314 | snp | A/C | | | intron-variant | LYN | GRCh38.p7 | 8:55944610 | ctcagcctcccgagt[A/C]cctgggattacaggc | 4067 |
rs7004881 | snp | C/T | 0.496175 | 0.0435625 | intron-variant | LYN | GRCh38.p7 | 8:55886303 | TGTAGTACAATGGTG[C/T]AATCTCCACTCACTG | 4067 |
rs7005312 | snp | C/T | 0.461259 | 0.133677 | intron-variant | LYN | GRCh38.p7 | 8:55893880 | CGATTATCACTCACA[C/T]ACTATGGTCCTGAGA | 4067 |
rs7005344 | snp | A/G | 0.105924 | 0.204309 | intron-variant | LYN | GRCh38.p7 | 8:55911484 | TACTCAAGGAATTGC[A/G]TGAACCATCTCTTTT | 4067 |
rs7005346 | snp | C/G | 0.162581 | 0.234218 | intron-variant | LYN | GRCh38.p7 | 8:55911486 | CTCAAGGAATTGCGT[C/G]AACCATCTCTTTTGT | 4067 |
rs7006830 | snp | C/T | | | intron-variant | LYN | GRCh38.p7 | 8:55941737 | TTTGAGTTTATTAAT[C/T]TATATATGATAAAGA | 4067 |
rs7010047 | snp | C/T | 0 | 0 | utr-variant-3-prime | LYN | GRCh38.p7 | 8:56012434 | CTATTTTAAAAGCTT[C/T]TCCAGTCagctagac | 4067 |
rs7012039 | snp | G/T | 0.095934 | 0.196885 | intron-variant | LYN | GRCh38.p7 | 8:55900082 | AATGCGCTGCCACTC[G/T]AACTTCAGGAAGACA | 4067 |
rs7012374 | snp | A/G | 0.095934 | 0.196885 | intron-variant | LYN | GRCh38.p7 | 8:55900282 | AGTGTCAAGCCAGTT[A/G]AGTTTTCTGCATTAA | 4067 |
rs7013185 | snp | C/G | 0.095934 | 0.196885 | intron-variant | LYN | GRCh38.p7 | 8:55900088 | CTGCCACTCGAACTT[C/G]AGGAAGACAAGAGCT | 4067 |
rs7014639 | snp | A/G | | | intron-variant | LYN | GRCh38.p7 | 8:55953466 | agcctggccaacgta[A/G]taaaattctgtctct | 4067 |
rs7341608 | snp | C/T | 0.331179 | 0.236453 | intron-variant | LYN | GRCh38.p7 | 8:55926941 | ctgcagttttagatt[C/T]agataaattaggcag | 4067 |
rs7341667 | snp | A/C | 0.126909 | 0.217598 | intron-variant | LYN | GRCh38.p7 | 8:55924611 | tcacgtaatccaccc[A/C]ccttggcctcccaaa | 4067 |
rs7461528 | snp | A/G | | | intron-variant | LYN | GRCh38.p7 | 8:55942401 | tatatatgtgtatat[A/G]tgtgtatatatatgt | 4067 |
rs7461530 | snp | A/G | | | intron-variant | LYN | GRCh38.p7 | 8:55942413 | tatatgtgtatatat[A/G]tgtgtgtatatatat | 4067 |
rs7461533 | snp | A/G | | | intron-variant | LYN | GRCh38.p7 | 8:55942431 | TGTGTATATATATAT[A/G]TGTGTGTGTGTGTAT | 4067 |
rs7463904 | snp | C/T | 0.030278 | 0.119257 | intron-variant | LYN | GRCh38.p7 | 8:55993983 | TTCTGTAGTGCTGAA[C/T]GCTACATGGCCCTGG | 4067 |
rs7464415 | snp | A/G | | | intron-variant | LYN | GRCh38.p7 | 8:55942405 | tatgtgtatatatgt[A/G]tatatatatgtgtgt | 4067 |
rs7464416 | snp | A/G | | | intron-variant | LYN | GRCh38.p7 | 8:55942419 | tgtatatatatgtgt[A/G]tatatatatatatgt | 4067 |
rs7464418 | snp | A/G | | | intron-variant | LYN | GRCh38.p7 | 8:55942443 | tatatgtgtgtgtgt[A/G]tatatatatatatat | 4067 |
rs7812431 | snp | A/G | 0.146985 | 0.227789 | intron-variant | LYN | GRCh38.p7 | 8:55950077 | atgttttcaaagttc[A/G]tccctgttgtagcat | 4067 |
rs7812680 | snp | C/T | 0.370365 | 0.219117 | intron-variant | LYN | GRCh38.p7 | 8:56004217 | gattacaggtgtgag[C/T]caccgcacccggccT | 4067 |
rs7813271 | snp | A/G | 0.296842 | 0.245572 | intron-variant | LYN | GRCh38.p7 | 8:55950592 | CATCTTGGTGGCTTT[A/G]TTTGCCACATTGGAT | 4067 |
rs7815149 | snp | C/T | 0.183886 | 0.241099 | intron-variant | LYN | GRCh38.p7 | 8:55955314 | TCTTTCTGCACATAT[C/T]TGCAGAATTCAGGTA | 4067 |
rs7815650 | snp | A/G | 0.392696 | 0.205275 | intron-variant | LYN | GRCh38.p7 | 8:55907636 | CTTTGAGAGACCCAC[A/G]TGGAAGGATTGCTTG | 4067 |
rs7815660 | snp | A/G | 0.388964 | 0.20782 | intron-variant | LYN | GRCh38.p7 | 8:55907659 | ATTGCTTGAGCCCAG[A/G]AGTTCAAGACCAGCC | 4067 |
rs7815680 | snp | C/G | 0.0520825 | 0.152737 | intron-variant | LYN | GRCh38.p7 | 8:56002028 | gctcacacgtgtaat[C/G]ctagcactttgggag | 4067 |
rs7816026 | snp | C/T | 0.309154 | 0.242901 | intron-variant | LYN | GRCh38.p7 | 8:56002291 | aggcgtggtggcagg[C/T]gcctgtagtcccagc | 4067 |
rs7816785 | snp | C/T | 0.471388 | 0.116136 | intron-variant | LYN | GRCh38.p7 | 8:55884859 | CTTTGTTGTTTATCC[C/T]CTTCATCCTGTTCTG | 4067 |
rs7817215 | snp | C/T | 0.5 | 0.000399361 | intron-variant | LYN | GRCh38.p7 | 8:55902030 | CTTTTTTTTTTGAGA[C/T]GAGTTTCACTCTTAT | 4067 |
rs7818679 | snp | C/T | 0.49334 | 0.057322 | intron-variant | LYN | GRCh38.p7 | 8:55895699 | GGACATTAGATGAAG[C/T]TCCTTCATCTAATGT | 4067 |
rs7818706 | snp | A/C | 0.0410537 | 0.137264 | intron-variant | LYN | GRCh38.p7 | 8:55960706 | AATACAATTAAAATT[A/C]TATCACTGTTAACCC | 4067 |
rs7819710 | snp | A/T | | | intron-variant | LYN | GRCh38.p7 | 8:55898298 | tatttttacttttaa[A/T]tttgttttgagacag | 4067 |
rs7820484 | snp | G/T | 0.164219 | 0.234823 | intron-variant | LYN | GRCh38.p7 | 8:55892918 | CAAAAAGCAGAATGA[G/T]GTTGACCCTCCCCCA | 4067 |
rs7820971 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | LYN | GRCh38.p7 | 8:55951008 | aacactttgggaggc[C/T]gaggcgagaggatca | 4067 |
rs7821714 | snp | A/G | 0.17332 | 0.23795 | intron-variant | LYN | GRCh38.p7 | 8:55896250 | actccagcctgggta[A/G]cagagcaagactctc | 4067 |
rs7823622 | snp | A/G | 0.106278 | 0.204558 | intron-variant | LYN | GRCh38.p7 | 8:55904939 | tgctcattagaatca[A/G]tggggagcatttaaa | 4067 |
rs7824121 | snp | C/T | 0.159292 | 0.232964 | intron-variant | LYN | GRCh38.p7 | 8:56009113 | TTTTTGAAAAATGTC[C/T]GTATAAGATAATATG | 4067 |
rs7824555 | snp | C/G | 0.198014 | 0.244535 | intron-variant | LYN | GRCh38.p7 | 8:55939187 | ACATGGAGGACCTCT[C/G]TTGAGGTTTCTGGTG | 4067 |
rs7825133 | snp | G/T | 0.046775 | 0.145601 | intron-variant | LYN | GRCh38.p7 | 8:56004500 | ggtttcaccatgttg[G/T]ccaggctggtcttga | 4067 |
rs7825881 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | LYN | GRCh38.p7 | 8:56004961 | agctaatttataaat[C/T]ttttgtagagacagg | 4067 |
rs7826509 | snp | A/G | 0.204803 | 0.245881 | intron-variant | LYN | GRCh38.p7 | 8:55992200 | GAAGAGAATCACATG[A/G]CCTAAGATGAAGAGA | 4067 |
rs7827321 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | LYN | GRCh38.p7 | 8:55955440 | AGCAGATTCATGGGT[A/G]TGAGTGCTCACTCTG | 4067 |
rs7827942 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | LYN | GRCh38.p7 | 8:55955180 | CCTCTACAGTCTTGG[C/T]CCCTGGGATCATAGC | 4067 |
rs7828258 | snp | C/T | 0.484066 | 0.0878235 | intron-variant | LYN | GRCh38.p7 | 8:55955386 | ATGTGTCAGAACTGG[C/T]TGGCAGTGCAAATCA | 4067 |
rs7828483 | snp | C/G | 0.384785 | 0.210554 | intron-variant | LYN | GRCh38.p7 | 8:55980329 | gcacaggagttttga[C/G]ctgctccgcttctga | 4067 |
rs7828619 | snp | C/T | 0.436834 | 0.166111 | intron-variant | LYN | GRCh38.p7 | 8:55897869 | AGTGAGTCGAGATCG[C/T]GCCACTGTACTCCAG | 4067 |
rs7829003 | snp | C/G | 0.286825 | 0.247273 | intron-variant | LYN | GRCh38.p7 | 8:55955804 | tctggcttatttcac[C/G]tagcataatgttttc | 4067 |
rs7829420 | snp | A/G | 0.339203 | 0.233544 | intron-variant | LYN | GRCh38.p7 | 8:55950880 | AAAAAAGGGCATATA[A/G]TATGCTCTGGTAGTA | 4067 |
rs7829816 | snp | A/G | 0.354665 | 0.227036 | intron-variant | LYN | GRCh38.p7 | 8:55936827 | TAAAAGCAACAAAAA[A/G]AGAAAAAGTACAGCT | 4067 |
rs7831223 | snp | A/G | 0.46754 | 0.123192 | intron-variant | LYN | GRCh38.p7 | 8:55897994 | AAAATGAAAATAGAC[A/G]ATTTTAAGAAAACTT | 4067 |
rs7831367 | snp | C/G | 0.242488 | 0.249887 | intron-variant | LYN | GRCh38.p7 | 8:55898120 | ACAGAAAAGTTCTGT[C/G]ACACCCTCCCCCCAA | 4067 |
rs7831638 | snp | C/T | 0.14933 | 0.228835 | intron-variant | LYN | GRCh38.p7 | 8:55880738 | CTGCCGAGGAGCAGT[C/T]CGGTGCTTTTGCCGG | 4067 |
rs7832713 | snp | A/G | 0.289942 | 0.246789 | intron-variant | LYN | GRCh38.p7 | 8:55954577 | AGCACAGTGGCTCAT[A/G]CCTGTAATCCCAGCA | 4067 |
rs7833156 | snp | C/T | 0.119978 | 0.213528 | intron-variant | LYN | GRCh38.p7 | 8:55936636 | cagagtgagactcca[C/T]ctcaaaaaacaaaca | 4067 |
rs7834059 | snp | A/G | 0.370162 | 0.219229 | intron-variant | LYN | GRCh38.p7 | 8:56002414 | acagagcgagactcc[A/G]tcttaaaaaaataaa | 4067 |
rs7834615 | snp | A/G | 0.497933 | 0.032082 | intron-variant | LYN | GRCh38.p7 | 8:55884881 | CCTGTTCTGTACTTC[A/G]TTTTCTCTCATTACT | 4067 |
rs7838485 | snp | A/C | 0.314544 | 0.241524 | intron-variant | LYN | GRCh38.p7 | 8:55973042 | GAGTAGAAATAACCC[A/C]GTTTACTTAATCCTA | 4067 |
rs7839010 | snp | C/T | 0.141258 | 0.225111 | intron-variant | LYN | GRCh38.p7 | 8:55960025 | ggcctgggagtatgg[C/T]aggagtgactgctaa | 4067 |
rs7840325 | snp | A/T | 0.484066 | 0.0878235 | intron-variant | LYN | GRCh38.p7 | 8:55896103 | AGGGGTAAAGCAATT[A/T]AAAaaaaaaaacaag | 4067 |
rs7843445 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | LYN | GRCh38.p7 | 8:55953506 | tataaaaactagctg[A/G]gcatagtggtgggca | 4067 |
rs7843459 | snp | A/G | 0.332568 | 0.235971 | intron-variant | LYN | GRCh38.p7 | 8:56004224 | ggtgtgagtcaccgc[A/G]cccggccTAAATATT | 4067 |
rs7844040 | snp | A/T | 0.196771 | 0.244268 | intron-variant | LYN | GRCh38.p7 | 8:55896179 | ggaggctgaagtgag[A/T]gggtcccttgagtcc | 4067 |
rs7844392 | snp | C/G | | | intron-variant | LYN | GRCh38.p7 | 8:55943430 | aaagtacaaaaatta[C/G]ccgggtgtggtggtg | 4067 |
rs7844404 | snp | A/G | 0.157972 | 0.232445 | intron-variant | LYN | GRCh38.p7 | 8:55943447 | cgggtgtggtggtgc[A/G]tgcctgtagtcccag | 4067 |
rs9298541 | snp | C/T | 0.417683 | 0.185425 | intron-variant | LYN | GRCh38.p7 | 8:55956358 | TTTTGTGAAGAGTGT[C/T]TAAGCACCTAAGCAG | 4067 |
rs9643487 | snp | A/G | 0.17461 | 0.238362 | intron-variant | LYN | GRCh38.p7 | 8:55896954 | CATGTTGGCCAGGTT[A/G]ATCTCAAACTCCTGA | 4067 |
rs9643488 | snp | C/T | 0.499 | 0.0223418 | intron-variant | LYN | GRCh38.p7 | 8:55896957 | GTTGGCCAGGTTAAT[C/T]TCAAACTCCTGACCT | 4067 |
rs9643489 | snp | C/G | 0.185788 | 0.241613 | intron-variant | LYN | GRCh38.p7 | 8:55897097 | AGCTGGTTGGAGAAC[C/G]ATGTTACTCACCCGA | 4067 |
rs9643490 | snp | A/G | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55939826 | AGAACTCCCATGCTT[A/G]CTTAGAGATCAACTC | 4067 |
rs9643839 | snp | A/T | 0.448066 | 0.152544 | intron-variant | LYN | GRCh38.p7 | 8:56008129 | GCCTCAAAAAAAAAA[A/T]AAAATAAAATAAAAT | 4067 |
rs9650314 | snp | A/G | 0.158302 | 0.232576 | intron-variant | LYN | GRCh38.p7 | 8:55991051 | AAATAGAGACACGCC[A/G]GCAGTACTACCACGT | 4067 |
rs10088887 | snp | C/T | 0.460477 | 0.134905 | intron-variant, downstream-variant-500B | LYN | GRCh38.p7 | 8:55968344 | CACTGCAACCTCTGC[C/T]TCCCAGGTTCCAGTG | 4067 |
rs10088996 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | LYN | GRCh38.p7 | 8:55959657 | ccattgtgagaaata[A/G]tacaaaaaggataac | 4067 |
rs10089762 | snp | A/G | 0.417845 | 0.185278 | intron-variant | LYN | GRCh38.p7 | 8:55956526 | AAATTTAGTTTCTCC[A/G]TGGCAACTTTTTACT | 4067 |
rs10089932 | snp | A/G | 0.311369 | 0.242351 | intron-variant | LYN | GRCh38.p7 | 8:55954398 | TTGAGGGTCACCAAG[A/G]AAGTTTCTAAGGTTC | 4067 |
rs10091244 | snp | G/T | 0.304438 | 0.244001 | intron-variant | LYN | GRCh38.p7 | 8:55931371 | ACAATGGAAAACATT[G/T]TTAAAATTTTAGACT | 4067 |
rs10091734 | snp | A/T | | | intron-variant | LYN | GRCh38.p7 | 8:55965538 | AAGAACACCTTTTTT[A/T]AAGAAAATGTGGTAA | 4067 |
rs10092290 | snp | A/G | 0.149665 | 0.228982 | intron-variant | LYN | GRCh38.p7 | 8:55911813 | agaggaatcaagggc[A/G]acttcttggttttaa | 4067 |
rs10093530 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | LYN | GRCh38.p7 | 8:56007830 | CATTTTAAAAAATAC[C/T]GGTAATTggctggat | 4067 |
rs10095555 | snp | A/G | 0.149665 | 0.228982 | intron-variant | LYN | GRCh38.p7 | 8:55912179 | AAATGTACTCCAAAG[A/G]AATTTGACTAAAGAA | 4067 |
rs10095917 | snp | C/T | 0.332106 | 0.236133 | intron-variant | LYN | GRCh38.p7 | 8:55917701 | TTCCAGTGTCTATTG[C/T]ATAATATGTTCAGGA | 4067 |
rs10100561 | snp | A/C | 0.329084 | 0.237162 | intron-variant | LYN | GRCh38.p7 | 8:55955059 | GTTGAGTGAAAGCAA[A/C]TGTGATTTCTAAATG | 4067 |
rs10101914 | snp | C/T | 0.342806 | 0.232136 | intron-variant | LYN | GRCh38.p7 | 8:55974128 | CTTGGCCAAGGTTAC[C/T]GAGCTAGTATGCGGA | 4067 |
rs10103164 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | LYN | GRCh38.p7 | 8:55934380 | TACCCGCTACTCCTT[G/T]GCAATCTTGTGTTTA | 4067 |
rs10104302 | snp | G/T | 0.335788 | 0.23482 | intron-variant | LYN | GRCh38.p7 | 8:55955681 | ATAAACAATCACTCT[G/T]CATTCGCCCCACCCT | 4067 |
rs10106451 | snp | C/T | 0.460365 | 0.13508 | intron-variant, downstream-variant-500B | LYN | GRCh38.p7 | 8:55968358 | CCTCCCAGGTTCCAG[C/T]GATTCTCCTGCCTCA | 4067 |
rs10112175 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | LYN | GRCh38.p7 | 8:55967418 | ctcccgggttcaagc[A/G]attctcctgcctcgg | 4067 |
rs10112370 | snp | C/T | 0.320575 | 0.239832 | intron-variant | LYN | GRCh38.p7 | 8:55974098 | ACCTCTTACAGATAA[C/T]GAGGTAAACTTGGAC | 4067 |
rs10282821 | snp | A/G | 0.232651 | 0.249397 | intron-variant | LYN | GRCh38.p7 | 8:55993509 | TGTGGTGTTAGAATC[A/G]TGGACTTTGAGGTCA | 4067 |
rs10504199 | snp | A/C | 0.105569 | 0.204058 | intron-variant | LYN | GRCh38.p7 | 8:55914050 | GCTTTTGGAAAGATA[A/C]GTGGACTAGCATGCA | 4067 |
rs10504200 | snp | A/C | 0.110872 | 0.20771 | intron-variant | LYN | GRCh38.p7 | 8:55930195 | CCACTGCTCTAGCTA[A/C]CCTAGACTCCTGATG | 4067 |
rs10696257 | in-del | -/GAG | 0.241627 | 0.24986 | intron-variant | LYN | GRCh38.p7 | 8:55906603 | TCAGGTAATCCACCT[-/GAG]GTCTCAGCCTCCCAA | 4067 |
rs10712449 | in-del | -/A | 0.197082 | 0.244335 | intron-variant | LYN | GRCh38.p7 | 8:55880409 | CGCGGGGGCGGGCTC[-/A]CCGCGTGTCCTTCCC | 4067 |
rs10958473 | snp | A/G | 0.493293 | 0.0575177 | intron-variant | LYN | GRCh38.p7 | 8:55894815 | tctgggattacaggc[A/G]tgagccaccatgcct | 4067 |
rs10958474 | snp | C/T | 0.493293 | 0.0575177 | intron-variant | LYN | GRCh38.p7 | 8:55894940 | CATGTGCTTCAGCCT[C/T]CCAAAGTGCTGGGAT | 4067 |
rs10958475 | snp | A/G | 0.45645 | 0.140991 | intron-variant | LYN | GRCh38.p7 | 8:55896439 | tgttcttactcataa[A/G]tgggagctgaacaat | 4067 |
rs11287133 | in-del | -/T | 0.266273 | 0.24947 | intron-variant | LYN | GRCh38.p7 | 8:55979051 | ATGCACTTCTCATTC[-/T]TTTTTTTTTTTTTTT | 4067 |
rs11326907 | in-del | -/C | 0.460589 | 0.13473 | intron-variant | LYN | GRCh38.p7 | 8:55968955 | TTCTTAGGTAGGTTT[-/C]CACTTTTTTCCAAAG | 4067 |
rs11354604 | in-del | -/G | 0.49334 | 0.057322 | intron-variant | LYN | GRCh38.p7 | 8:55895457 | CTTTGGGGTGTCTGA[-/G]GAGCAGCATGATGTC | 4067 |
rs11366178 | in-del | -/A | | | intron-variant | LYN | GRCh38.p7 | 8:55912727 | GTGAGACTCCATCTG[-/A]AAAAAAAAAAAAAAA | 4067 |
rs11384692 | in-del | -/G | 0.095934 | 0.196885 | intron-variant | LYN | GRCh38.p7 | 8:55900014 | GTACGAGGTGGAGCT[-/G]GAACTTGGGCCTAGG | 4067 |
rs11412762 | in-del | -/A | | | intron-variant | LYN | GRCh38.p7 | 8:55997175 | AAAAAAAAAAAAAAA[-/A]GAGTGAATCTTTGTG | 4067 |
rs11416891 | in-del | -/T | | | intron-variant | LYN | GRCh38.p7 | 8:55893800 | GTTTTGTTTTTTTTT[-/T]AGAAGCAAGATCTCA | 4067 |
rs11417223 | in-del | -/G | | | intron-variant | LYN | GRCh38.p7 | 8:55906748 | AAGAGAGAGAGAGGA[-/G]GAGAGAGAGAGAAAT | 4067 |
rs11417224 | in-del | -/A | | | intron-variant | LYN | GRCh38.p7 | 8:55906746 | AAAAGAGAGAGAGAG[-/A]GAGAGAGAGAGAGAA | 4067 |
rs11417225 | in-del | -/A | | | intron-variant | LYN | GRCh38.p7 | 8:55906725 | AAAAAAAAGAAAAAG[-/A]AAAAAAAAAAGAGAG | 4067 |
rs11424283 | in-del | -/T | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55902332 | CTTTTTTTTTTTTTT[-/T]GAGATGGAATTTCGC | 4067 |
rs11424284 | in-del | -/T/TT | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55902015 | CTTTCTTTTTTTTTT[-/T/TT]GAGACGAGTTTCACT | 4067 |
rs11438443 | in-del | -/A | | | intron-variant | LYN | GRCh38.p7 | 8:55943594 | AAAAAAAAAAAAAAA[-/A]GGCATTTTTATAGTT | 4067 |
rs11450642 | in-del | -/T | 0.479421 | 0.0993283 | intron-variant | LYN | GRCh38.p7 | 8:55965033 | CCCCATTTTTTTTTT[-/T]AACATTTCCAAGAGA | 4067 |
rs11776339 | snp | C/T | 0.497829 | 0.0328757 | intron-variant | LYN | GRCh38.p7 | 8:55887803 | TTAGTACAGACAGGG[C/T]TTTGCTGTGTTGGCC | 4067 |
rs11776414 | snp | G/T | | | intron-variant | LYN | GRCh38.p7 | 8:56007939 | gcctggccaacatgg[G/T]gaaaccccgtctcta | 4067 |
rs11781555 | snp | A/C | 0.220544 | 0.248259 | intron-variant | LYN | GRCh38.p7 | 8:55919052 | AAAAAAAAAAGTGAT[A/C]GTAGTCAGACATTCC | 4067 |
rs11783784 | snp | A/G | 0.498009 | 0.0314867 | intron-variant | LYN | GRCh38.p7 | 8:55887980 | GACTGCAGAAGGCAG[A/G]TGGAAGCAGACAGGG | 4067 |
rs11784200 | snp | A/T | 0.45946 | 0.136478 | intron-variant | LYN | GRCh38.p7 | 8:55896665 | ataataaaaaaattt[A/T]aaaaaaAAGAAACAT | 4067 |
rs11985083 | snp | C/G | 0.0722614 | 0.17581 | intron-variant | LYN | GRCh38.p7 | 8:55940302 | CCCAGAAGAGTTTCC[C/G]GGACAGTGTCCAGAG | 4067 |
rs11986508 | snp | A/G | | | intron-variant, upstream-variant-2KB | LYN | GRCh38.p7 | 8:55924093 | attatagcaaccaca[A/G]aaaacccagttttac | 4067 |
rs11987458 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | LYN | GRCh38.p7 | 8:55979075 | ttttttttttttgag[A/T]tggagttttgctctt | 4067 |
rs11987481 | snp | A/G | 0.204803 | 0.245881 | intron-variant | LYN | GRCh38.p7 | 8:55979186 | tagctgggattacaa[A/G]cgtgtgccaccacgc | 4067 |
rs11990283 | snp | G/T | 0.0539704 | 0.155153 | intron-variant | LYN | GRCh38.p7 | 8:55886258 | ttttttttttttttt[G/T]gagatggagtctcgc | 4067 |
rs11991299 | snp | G/T | 0.497271 | 0.0368399 | intron-variant | LYN | GRCh38.p7 | 8:55887212 | gtaatcccagcactc[G/T]gggagcatgaggcag | 4067 |
rs11992596 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | LYN | GRCh38.p7 | 8:55963118 | ggagaggacaaacat[C/T]caaactatatcagag | 4067 |
rs11993353 | snp | G/T | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55984450 | ATCTTCTCCCTTTTG[G/T]TGATGGCACCTCTGT | 4067 |
rs11993738 | snp | A/G | 0.492871 | 0.0592773 | intron-variant | LYN | GRCh38.p7 | 8:55890776 | tctgtcacccgggct[A/G]gagtgtggtggcacc | 4067 |
rs11995242 | snp | C/T | 0.492775 | 0.059668 | intron-variant | LYN | GRCh38.p7 | 8:55890980 | gcaatctacctgctg[C/T]ggcctcccaaagtgc | 4067 |
rs11996228 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | LYN | GRCh38.p7 | 8:55977824 | ctcaggaggctgaga[C/T]gagaggattgatcga | 4067 |
rs11996440 | snp | C/T | 0.173965 | 0.238157 | utr-variant-5-prime | LYN | GRCh38.p7 | 8:55877397 | gccactgagctcagT[C/T]gcttgggggccattt | 4067 |
rs11998041 | snp | C/T | 0.093417 | 0.194889 | intron-variant | LYN | GRCh38.p7 | 8:55979018 | AAATGTGATTTTTCT[C/T]TGTACTTAAATGAAA | 4067 |
rs11998707 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | LYN | GRCh38.p7 | 8:55962800 | gtttatttgctttac[A/G]gttcttcagatttta | 4067 |
rs12114560 | snp | C/T | 0.117537 | 0.212022 | intron-variant | LYN | GRCh38.p7 | 8:55961929 | gctattccgaccttc[C/T]tgatggttttctgac | 4067 |
rs12155838 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LYN | GRCh38.p7 | 8:55895653 | TAAAGGAATTGGCTT[C/T]TAGTCAATGCTTTGT | 4067 |
rs12334430 | snp | A/T | 0.364193 | 0.222396 | intron-variant | LYN | GRCh38.p7 | 8:55947401 | TATTTATAGTTTTAG[A/T]TTTAAGTGATTTGCA | 4067 |
rs12542445 | snp | G/T | 0.162581 | 0.234218 | intron-variant | LYN | GRCh38.p7 | 8:55907454 | TGGGCCTGTGAGGTG[G/T]CAAGGAAGCTCTGTG | 4067 |
rs12543920 | snp | C/T | 0.393987 | 0.204372 | intron-variant | LYN | GRCh38.p7 | 8:55909404 | GCCATAGGTTCCACC[C/T]GAGTGGGATTCTGAC | 4067 |
rs12545621 | snp | A/G | 0.393987 | 0.204372 | intron-variant | LYN | GRCh38.p7 | 8:55909386 | TGGAGGCTCTGTGGC[A/G]CTGCCATAGGTTCCA | 4067 |
rs12546061 | snp | C/T | | | intron-variant | LYN | GRCh38.p7 | 8:55927735 | cagctactcaggaga[C/T]tgaggcaggagaatt | 4067 |
rs12675828 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | LYN | GRCh38.p7 | 8:55917218 | AAAGATGGGATCTTG[C/T]GCTGTCACCCAGGCT | 4067 |
rs12675846 | snp | A/G | 0.293037 | 0.246268 | intron-variant | LYN | GRCh38.p7 | 8:55934986 | TGACACCTAACCATC[A/G]AAGCAGCTCTGTGGT | 4067 |
rs12676105 | snp | C/T | 0.498503 | 0.0273153 | intron-variant | LYN | GRCh38.p7 | 8:55882880 | CTCTTTCTACTTGTC[C/T]ACCTTTGGACTTGTA | 4067 |
rs12678598 | snp | C/T | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55897677 | agcactttgggaggc[C/T]gaggcaggaagatca | 4067 |
rs12678730 | snp | C/T | 0.493154 | 0.0581045 | intron-variant | LYN | GRCh38.p7 | 8:55892419 | agcaagactccatct[C/T]aaaaaaataaataca | 4067 |
rs12678731 | snp | A/C | 0.191461 | 0.24305 | intron-variant | LYN | GRCh38.p7 | 8:55892433 | tcaaaaaaataaata[A/C]ataaaaaaGTTGCAT | 4067 |
rs12679127 | snp | C/T | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55963274 | gaatcttcagctctt[C/T]taagttattgccaac | 4067 |
rs12679916 | snp | C/T | 0.492679 | 0.0600586 | intron-variant | LYN | GRCh38.p7 | 8:55894404 | GAGACAGTGGTCACT[C/T]TGTCACCCAAACTTA | 4067 |
rs12680741 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYN | GRCh38.p7 | 8:55936380 | cgtggtggctcattc[C/G]tataatcccagcact | 4067 |
rs13248269 | snp | A/C | | | intron-variant | LYN | GRCh38.p7 | 8:55934604 | AGAATGAGGGGAGCC[A/C]TGGGACAGCATCTGG | 4067 |
rs13248949 | snp | A/G | | | intron-variant | LYN | GRCh38.p7 | 8:55888704 | GTGACCTGGAGAGTG[A/G]CAGATACAGTAATGG | 4067 |
rs13248953 | snp | A/C | | | intron-variant | LYN | GRCh38.p7 | 8:55888710 | TGGAGAGTGACAGAT[A/C]CAGTAATGGGCACAA | 4067 |
rs13248963 | snp | A/C/G | | | intron-variant | LYN | GRCh38.p7 | 8:55888712 | GAGAGTGACAGATAC[A/C/G]GTAATGGGCACAATC | 4067 |
rs13249045 | snp | A/T | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55934532 | GTTAAATGGACACCC[A/T]CCGTGCAAGTGCATG | 4067 |
rs13249338 | snp | A/G | 0.495368 | 0.0478996 | intron-variant | LYN | GRCh38.p7 | 8:55934611 | GGGGAGCCCTGGGAC[A/G]GCATCTGGCTGTTTT | 4067 |
rs13249537 | snp | C/G | 0 | 0 | intron-variant, upstream-variant-2KB | LYN | GRCh38.p7 | 8:55922548 | gggaggccgaggcgg[C/G]tgaattctcaagagt | 4067 |
rs13252782 | snp | G/T | 0.393987 | 0.204372 | intron-variant | LYN | GRCh38.p7 | 8:55909141 | CATGGCGAATTTGCT[G/T]CTCTGCTAAGTAGGA | 4067 |
rs13253060 | snp | G/T | 0.393987 | 0.204372 | intron-variant | LYN | GRCh38.p7 | 8:55909236 | CGTGATGGGCCAGGG[G/T]GCGACTGCATTTCCA | 4067 |
rs13256231 | snp | A/T | | | intron-variant | LYN | GRCh38.p7 | 8:55888690 | GACACCTCCCCTAAG[A/T]GACCTGGAGAGTGAC | 4067 |
rs13257714 | snp | A/G | 0.25214 | 0.249991 | intron-variant | LYN | GRCh38.p7 | 8:55964998 | ACTGCAGGAAGATTT[A/G]CAGTGACACCAGCAG | 4067 |
rs13264109 | snp | G/T | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55984076 | acctctgtcttccgg[G/T]ggcctctgaccttcc | 4067 |
rs13265447 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LYN | GRCh38.p7 | 8:55902825 | TTGGACACCTTGATC[A/G]ACAGTGCCCATTCTC | 4067 |
rs13267131 | snp | C/T | 0.209388 | 0.246679 | intron-variant | LYN | GRCh38.p7 | 8:55898417 | tctcagcctcccaag[C/T]agctgagaccacagg | 4067 |
rs13267469 | snp | A/C | | | intron-variant | LYN | GRCh38.p7 | 8:55920754 | ttggctcactgcaag[A/C]tccgcccctcccccc | 4067 |
rs13270094 | snp | A/G | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55957344 | CAATTTTAATCATAA[A/G]ACAGAGCCATAAATA | 4067 |
rs13272552 | snp | C/T | | | intron-variant | LYN | GRCh38.p7 | 8:55887534 | acatataaatatata[C/T]ataaatcccatataa | 4067 |
rs13274372 | snp | C/G | 0.492871 | 0.0592773 | intron-variant | LYN | GRCh38.p7 | 8:55891311 | gagtcgagatcccgc[C/G]actgcactccagcca | 4067 |
rs13274397 | snp | A/G | 0.493201 | 0.0579089 | intron-variant | LYN | GRCh38.p7 | 8:55891340 | cagggcaacaagagc[A/G]aaactccggctcaaa | 4067 |
rs13277429 | snp | C/T | 0.492871 | 0.0592773 | intron-variant | LYN | GRCh38.p7 | 8:55891630 | GGTGTGATGGTTATA[C/T]AAGAATATGAATGTA | 4067 |
rs13279092 | snp | A/T | 0.173965 | 0.238157 | intron-variant | LYN | GRCh38.p7 | 8:55894136 | CCATACCCCAAGAGA[A/T]CATGCTGAGCCTGTA | 4067 |
rs13279481 | snp | C/T | 0.393987 | 0.204372 | intron-variant | LYN | GRCh38.p7 | 8:55909250 | GTGCGACTGCATTTC[C/T]AGCTGCACCCTGTTT | 4067 |
rs13279662 | snp | A/G | 0.277778 | 0.248452 | intron-variant | LYN | GRCh38.p7 | 8:55908991 | TTCCATTGTGTATGT[A/G]TATATATATATATAT | 4067 |
rs13279909 | snp | A/C | 0.462363 | 0.131916 | intron-variant | LYN | GRCh38.p7 | 8:55909051 | CACACACACACACAC[A/C]CCCCACATTTTCTTT | 4067 |
rs13280789 | snp | A/G | | | intron-variant | LYN | GRCh38.p7 | 8:55888703 | AGTGACCTGGAGAGT[A/G]ACAGATACAGTAATG | 4067 |
rs13280917 | snp | G/T | | | intron-variant | LYN | GRCh38.p7 | 8:55926089 | TTATCACTTTCAAGG[G/T]GATTCTTGCACATAA | 4067 |
rs13280991 | snp | A/T | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55887561 | ataaaaatataaata[A/T]atatatatatatata | 4067 |
rs13280999 | snp | A/T | 0.375 | 0.216506 | intron-variant | LYN | GRCh38.p7 | 8:55887569 | ataaatatatatata[A/T]atatatacacacaca | 4067 |
rs13282655 | snp | A/C | 0.497211 | 0.037236 | intron-variant | LYN | GRCh38.p7 | 8:55888642 | GACAGCAATAGGCTT[A/C]AGCTTGTAATCGTCA | 4067 |
rs13282671 | snp | C/G | | | intron-variant | LYN | GRCh38.p7 | 8:55888662 | TGTAATCGTCATCTG[C/G]AAGTAGGTACTTGAC | 4067 |
rs13282751 | snp | A/C | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55934482 | CCGTTCACCGGCCCG[A/C]TAAGATTTGACTGGG | 4067 |
rs13282982 | snp | C/T | 0.499809 | 0.00978247 | intron-variant | LYN | GRCh38.p7 | 8:55896630 | tgcatgttcggcaca[C/T]gtatcttagaaatta | 4067 |
rs16919981 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | LYN | GRCh38.p7 | 8:55957258 | CTGACTCCGTGTGCC[C/T]TATTTTTATTATTGT | 4067 |
rs16920156 | snp | C/T | 0.078151 | 0.181571 | intron-variant | LYN | GRCh38.p7 | 8:55981267 | CATTCTCCTCAGTCT[C/T]GGTCCCCGCCCATTT | 4067 |
rs16920168 | snp | C/T | 0.0799831 | 0.183287 | intron-variant | LYN | GRCh38.p7 | 8:55982717 | CCCCACCTTCAAATG[C/T]TGGCTTCTCTGTGTC | 4067 |
rs16920172 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | LYN | GRCh38.p7 | 8:55985207 | AAGTGAGTGAAACCC[A/C]GTAATTGTTTGCTGA | 4067 |
rs16920176 | snp | C/T | 0.206947 | 0.246265 | intron-variant | LYN | GRCh38.p7 | 8:55986577 | CTCCCTAAGGCATTG[C/T]GGGTCCTTGCATGCT | 4067 |
rs16920180 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | LYN | GRCh38.p7 | 8:55987892 | CTACTTTATGGGCTT[A/G]TTTTAACGACTAACA | 4067 |
rs16920186 | snp | C/T | 0.206029 | 0.246103 | intron-variant | LYN | GRCh38.p7 | 8:55988159 | GAGATTAGAGGAATC[C/T]AGTGTTGGGGAATCA | 4067 |
rs16920192 | snp | A/T | 0.336245 | 0.234652 | intron-variant | LYN | GRCh38.p7 | 8:55991467 | AAAGGCCACTCTAGA[A/T]GACTGGAAGTCTATC | 4067 |
rs16920208 | snp | C/T | 0.115788 | 0.21092 | utr-variant-3-prime | LYN | GRCh38.p7 | 8:56012311 | GTGTGCAAAATGGCT[C/T]ATGTCATCACACCTC | 4067 |
rs16922309 | snp | C/T | 0.119281 | 0.213102 | intron-variant | LYN | GRCh38.p7 | 8:55888132 | TGCTATGTTTAGTAT[C/T]CAGTTTAGCAAACTT | 4067 |
rs16922312 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | LYN | GRCh38.p7 | 8:55892481 | TGCTTCCTGATTTGA[C/T]GATACAGTTATATTA | 4067 |
rs16922353 | snp | A/T | 0.095934 | 0.196885 | intron-variant | LYN | GRCh38.p7 | 8:55899175 | TTTCACAGAAAATAT[A/T]GTAAGAATAGCAATC | 4067 |
rs16922355 | snp | C/T | 0.095934 | 0.196885 | intron-variant | LYN | GRCh38.p7 | 8:55899214 | AATATTTGTCCTCTG[C/T]TAGGTAGTCAATTCC | 4067 |
rs16922391 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | LYN | GRCh38.p7 | 8:55912998 | AGAATTGATGATGCT[A/G]CTTATTAAAAATGAC | 4067 |
rs16922396 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | LYN | GRCh38.p7 | 8:55913672 | GTACTGAGTAGAATA[A/G]GACGTGAGACAAGTG | 4067 |
rs16922398 | snp | A/G | 0.105924 | 0.204309 | intron-variant | LYN | GRCh38.p7 | 8:55914175 | GGGAAATAAGAGAAA[A/G]GCAGGCCAGGTCAGA | 4067 |
rs16922400 | snp | C/T | 0.079617 | 0.182947 | intron-variant | LYN | GRCh38.p7 | 8:55915180 | GTTGCAGCTGTCCAA[C/T]CTCTCTGGCATTCTA | 4067 |
rs16922408 | snp | G/T | 0.0803491 | 0.183626 | intron-variant | LYN | GRCh38.p7 | 8:55921107 | AGATACGTCTGAAAC[G/T]AAAACAATTTTGGGA | 4067 |
rs16922412 | snp | A/C/T | 0.0209421 | 0.100162 | intron-variant, upstream-variant-2KB | LYN | GRCh38.p7 | 8:55923273 | CTCCTAATGGCAGTG[A/C/T]GGGCAATGTGAGAGA | 4067 |
rs16922415 | snp | C/T | 0.115788 | 0.21092 | intron-variant | LYN | GRCh38.p7 | 8:55926546 | TTATCAGTTATTTTC[C/T]GAACCTAAAATTGAA | 4067 |
rs16922422 | snp | C/G | 0.117537 | 0.212022 | intron-variant | LYN | GRCh38.p7 | 8:55933213 | AGCTGTTAAAACTAT[C/G]CCATCTAATATGACA | 4067 |
rs16922425 | snp | C/T | 0.484279 | 0.0872533 | intron-variant | LYN | GRCh38.p7 | 8:55933710 | GTCTCATTATCCTCT[C/T]TGCACTCCCTTCCAG | 4067 |
rs16922428 | snp | C/G | 0.0310518 | 0.120672 | intron-variant | LYN | GRCh38.p7 | 8:55934305 | ACAGCTTAAGTTTGC[C/G]AACAGGGTTTGAATC | 4067 |
rs16922431 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | LYN | GRCh38.p7 | 8:55934475 | GTGTATGCCGTTCAC[C/T]GGCCCGCTAAGATTT | 4067 |
rs16922433 | snp | A/G | 0.197703 | 0.244469 | intron-variant | LYN | GRCh38.p7 | 8:55936340 | AGACCTTGCATCAGT[A/G]AAGAAGTGCAGCTTT | 4067 |
rs16922434 | snp | A/G | 0.201418 | 0.245234 | intron-variant | LYN | GRCh38.p7 | 8:55936863 | GCCAGACCAAGTTCC[A/G]GTTGTACCTGAGACC | 4067 |
rs16922437 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | LYN | GRCh38.p7 | 8:55937662 | TTATGAAACCAAAAC[C/T]CTACTGCCTCTGGTA | 4067 |
rs16922439 | snp | C/T | 0.0962929 | 0.197165 | intron-variant | LYN | GRCh38.p7 | 8:55938443 | TAAGCAAACTTGGAA[C/T]TCCTGTTGGGGACAC | 4067 |
rs16922441 | snp | C/G | 0.292266 | 0.246401 | intron-variant | LYN | GRCh38.p7 | 8:55938773 | ATGCATTTCAAAATA[C/G]CCATTGTATGGCAAA | 4067 |
rs16922451 | snp | C/T | 0.0829062 | 0.185956 | intron-variant | LYN | GRCh38.p7 | 8:55941104 | TTCCTAGGCCCCTAC[C/T]TATGTTTAGCTGGAG | 4067 |
rs16922458 | snp | G/T | 0.263809 | 0.249618 | intron-variant | LYN | GRCh38.p7 | 8:55941472 | MCTGGCTGCCATCCC[G/T]CCCATTTCAACTCAC | 4067 |
rs16922459 | snp | C/T | 0.202343 | 0.245416 | intron-variant | LYN | GRCh38.p7 | 8:55941613 | TTTGCCACAAGAATA[C/T]GAGCAGAGTTAGAGC | 4067 |
rs16922461 | snp | A/G | 0.302435 | 0.244439 | intron-variant | LYN | GRCh38.p7 | 8:55947466 | TACTCTCTGTGGGCC[A/G]TGCAGACCCTGAGCC | 4067 |
rs16922462 | snp | C/T | 0.313814 | 0.241719 | intron-variant | LYN | GRCh38.p7 | 8:55948406 | ATGGGCCCAGCCTAG[C/T]TTGAGTTCTAAGGGT | 4067 |
rs16922463 | snp | A/C | 0.325799 | 0.238232 | intron-variant | LYN | GRCh38.p7 | 8:55949110 | GACTCGAGCATGGTG[A/C]TGAAGCTCACTTGCT | 4067 |
rs16922464 | snp | A/G | 0.14665 | 0.227637 | intron-variant | LYN | GRCh38.p7 | 8:55949183 | CTATGATAACTAGAT[A/G]TTTGAACAAAGGAGT | 4067 |
rs16922466 | snp | A/G | 0.145978 | 0.227331 | intron-variant | LYN | GRCh38.p7 | 8:55949363 | TGATCGCAGTGATGC[A/G]TGCTTTAGTTGTAAG | 4067 |
rs16922470 | snp | C/T | 0.148326 | 0.228391 | intron-variant | LYN | GRCh38.p7 | 8:55950928 | TAACAAATAACAAAC[C/T]TCAGTGATTAGTTGT | 4067 |
rs16922471 | snp | A/G | 0.103438 | 0.202533 | intron-variant | LYN | GRCh38.p7 | 8:55951314 | TGGCCAGTTCTTACC[A/G]GGCTTTGTTTGCTGA | 4067 |
rs16922472 | snp | A/T | 0.200492 | 0.245049 | intron-variant | LYN | GRCh38.p7 | 8:55953318 | TGTTAGCAGTGCTGA[A/T]GAATACAATCAAGTA | 4067 |
rs16922476 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | LYN | GRCh38.p7 | 8:55954500 | CAAGATTATAGCAGT[G/T]GCTTTTTCCAGGGGA | 4067 |
rs16922478 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | LYN | GRCh38.p7 | 8:55955285 | TCATTAATTAATTCT[C/T]ACTGCACTGTAAGTC | 4067 |
rs16922484 | snp | C/T | 0.123452 | 0.215605 | intron-variant | LYN | GRCh38.p7 | 8:55956764 | TCTGCGTTCTCTTCC[C/T]GGCTTCTCCGTCTGT | 4067 |
rs16922494 | snp | G/T | 0.319136 | 0.24025 | intron-variant | LYN | GRCh38.p7 | 8:55972036 | AGGTCGGCACCAGTG[G/T]TCTCCATCCAAGCCA | 4067 |
rs16922495 | snp | A/C | 0.0383715 | 0.133092 | intron-variant | LYN | GRCh38.p7 | 8:55972116 | GGTCTCTTTCCTAGC[A/C]GTGGCCCCTTGGTGG | 4067 |
rs16922497 | snp | G/T | 0.0279526 | 0.114869 | intron-variant | LYN | GRCh38.p7 | 8:55972192 | CTGGGAGAGTCACGG[G/T]TCAGCAGCAGCCGGC | 4067 |
rs16922499 | snp | A/T | 0.046775 | 0.145601 | intron-variant | LYN | GRCh38.p7 | 8:55973532 | ATGTCAGAGAAGAAA[A/T]ATGAACTTGGAAAGA | 4067 |
rs16922502 | snp | C/T | 0.323434 | 0.238972 | intron-variant | LYN | GRCh38.p7 | 8:55974877 | AGATGTCGAGTCAGA[C/T]GTGGTGGCAAGTGGA | 4067 |
rs16922504 | snp | A/G | 0.097727 | 0.198275 | intron-variant | LYN | GRCh38.p7 | 8:55975571 | AATAAGGGAACACAA[A/G]TATATCACTTTAATG | 4067 |
rs16922508 | snp | C/T | 0.384593 | 0.210677 | intron-variant | LYN | GRCh38.p7 | 8:55979671 | GCATTCCCCAGGTTT[C/T]GCTGAGGTTCCCATC | 4067 |
rs17515910 | snp | A/C | 0.26326 | 0.249648 | intron-variant | LYN | GRCh38.p7 | 8:55941457 | TTGCTGACTTTGCAA[A/C]CTGGCTGCCATCCCK | 4067 |
rs17515924 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | LYN | GRCh38.p7 | 8:55941514 | TTTAGGAAGCTTTCC[C/T]TGACCACCTCCTTTT | 4067 |
rs17756527 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | LYN | GRCh38.p7 | 8:55988957 | AATTTCTCAAAAAGC[A/G]ATAGTAATTAGGATG | 4067 |
rs17811397 | snp | G/T | 0.134119 | 0.221521 | intron-variant | LYN | GRCh38.p7 | 8:55949209 | GGAGTTTATAATGCA[G/T]GAACTGTGGACCAGT | 4067 |
rs17812274 | snp | A/G | 0.256061 | 0.249927 | intron-variant | LYN | GRCh38.p7 | 8:55970578 | TTATAGAAGTTCTAG[A/G]GAAGACTGGTCCCTA | 4067 |
rs17812659 | snp | A/G | 0.15698 | 0.23205 | intron-variant | LYN | GRCh38.p7 | 8:55977303 | AAAATAAAAATGCTT[A/G]TACTCAGCAAATAGT | 4067 |
rs17812677 | snp | A/T | 0.251578 | 0.249995 | intron-variant | LYN | GRCh38.p7 | 8:55978005 | CTGAGCTTTTTCAAT[A/T]CAGAGCTAGATTCTC | 4067 |
rs28373742 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | LYN | GRCh38.p7 | 8:55930841 | CAGGACCTTGGCAGG[A/G]CCTGTTTCTTTTACC | 4067 |
rs28396906 | snp | C/T | 0.152001 | 0.229992 | intron-variant | LYN | GRCh38.p7 | 8:55885427 | ATCTTGCTCACTCCT[C/T]TTTATTGACACCAGA | 4067 |
rs28416311 | snp | A/T | 0.0554779 | 0.157039 | intron-variant | LYN | GRCh38.p7 | 8:55982391 | TTGAATCTTGGAGCA[A/T]TATGGATTTTGGGTT | 4067 |
rs28450840 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | LYN | GRCh38.p7 | 8:55919937 | GTGGGAGCTTTGTCA[C/T]GTGACCCCACTCTTT | 4067 |
rs28452438 | snp | A/T | | | intron-variant | LYN | GRCh38.p7 | 8:55964569 | AAAAAAATCATTTTT[A/T]AAAAAGTACATACTT | 4067 |
rs28520491 | snp | C/G | 0.399073 | 0.200692 | intron-variant | LYN | GRCh38.p7 | 8:55891420 | AGGACATCATGCTAA[C/G]TGAAATAAGCCAGAC | 4067 |
rs28553424 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | LYN | GRCh38.p7 | 8:55975116 | ATCTGAGCCGGGTGC[C/T]GCTGTGGATTCAGGG | 4067 |
rs28595219 | snp | C/T | 0.289424 | 0.246872 | intron-variant | LYN | GRCh38.p7 | 8:55884698 | GACCTTAGGTGAGCC[C/T]GCCTCGGCCTCCCAA | 4067 |
rs28604369 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | LYN | GRCh38.p7 | 8:55981388 | TAGATGCTCAAAAAT[A/G]CTTGTTGGATGACTA | 4067 |
rs28613969 | snp | C/G | 0.486133 | 0.082104 | intron-variant | LYN | GRCh38.p7 | 8:55924178 | TACCTTGAGTGAGTA[C/G]CTCTCACGATGTGTG | 4067 |
rs28684661 | snp | A/G | 0.149665 | 0.228982 | intron-variant | LYN | GRCh38.p7 | 8:55908189 | TTAAAGGTGATAAGG[A/G]CATCAATTCCCAGAC | 4067 |
rs28701843 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | LYN | GRCh38.p7 | 8:55969663 | ATGTGAATTTTGTTT[A/G]GATTTTTTCTTGTGT | 4067 |
rs28756452 | snp | A/T | 0.462363 | 0.131916 | intron-variant | LYN | GRCh38.p7 | 8:55890721 | GTGGTTTATATGTAC[A/T]TTGGAATTTTTTTTT | 4067 |
rs28857570 | snp | C/T | 0.445724 | 0.155538 | intron-variant | LYN | GRCh38.p7 | 8:55898241 | ATATAAATAGATTCA[C/T]ACTGTATGTGATCGT | 4067 |
rs34130107 | in-del | -/T | 0.496314 | 0.0427728 | intron-variant | LYN | GRCh38.p7 | 8:55894537 | ACTACACCTGGCTAA[-/T]TTTTTTTTTTTTTTT | 4067 |
rs34154931 | in-del | -/C | | | intron-variant | LYN | GRCh38.p7 | 8:55928443 | AGCCACCACGCAGGG[-/C]CCCATTGTTGCTTTA | 4067 |
rs34202602 | in-del | -/T | | | intron-variant | LYN | GRCh38.p7 | 8:55965514 | AGTATATATAAGTAA[-/T]TTTTTATAAAGAACA | 4067 |
rs34279138 | snp | C/T | 0.301429 | 0.244653 | intron-variant | LYN | GRCh38.p7 | 8:55935511 | GGGTGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 4067 |
rs34321980 | in-del | -/G | | | intron-variant | LYN | GRCh38.p7 | 8:56008211 | GTTGATCCCAAATGC[-/G]GGATAGTGCCCCGCA | 4067 |
rs34326950 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | LYN | GRCh38.p7 | 8:55958030 | GCTGTGGTGTCAGTG[C/T]GTCCTGCAGGGGGTG | 4067 |
rs34331544 | in-del | -/A | | | intron-variant | LYN | GRCh38.p7 | 8:55908793 | TTCCACATTCTGTGT[-/A]CCATGTGTGCAGATT | 4067 |
rs34349116 | in-del | -/G | | | intron-variant | LYN | GRCh38.p7 | 8:55989194 | ACCGTGTGGGATGCT[-/G]GGGGTTGACAGACTT | 4067 |
rs34445808 | in-del | -/G | | | intron-variant | LYN | GRCh38.p7 | 8:55958684 | AATTTGACTACCTTA[-/G]GTACCTCAAATAATT | 4067 |
rs34453579 | snp | C/T | 0.393065 | 0.205018 | intron-variant | LYN | GRCh38.p7 | 8:55911057 | GCCCACCTCCATGTC[C/T]GGCTAATTTATATAT | 4067 |
rs34461698 | in-del | -/A | | | intron-variant | LYN | GRCh38.p7 | 8:55990240 | TGAGACTCTGCCTCC[-/A]AAAAAAAAAAAAAAA | 4067 |
rs34484836 | in-del | -/T | 0.417034 | 0.18601 | intron-variant | LYN | GRCh38.p7 | 8:55966368 | AATTTTTTTTTTTTT[-/T]AATTGAGACGGAGTC | 4067 |
rs34561175 | snp | G/T | | | intron-variant | LYN | GRCh38.p7 | 8:55884574 | GATTCTCCTGCCTCA[G/T]CCTCCCTAGTAGCTG | 4067 |
rs34567274 | in-del | -/G | | | intron-variant | LYN | GRCh38.p7 | 8:55983787 | TAAACCTTGCAATGT[-/G]CCCAGAACTCACTCT | 4067 |
rs34595432 | in-del | -/G | | | intron-variant, upstream-variant-2KB | LYN | GRCh38.p7 | 8:55922354 | TCAGCCTCCCCAAGT[-/G]GCTGGGATTATAGGC | 4067 |
rs34622938 | in-del | -/G | | | intron-variant | LYN | GRCh38.p7 | 8:55936607 | TCGCGCCATTGCACT[-/G]CCAGCCTGGGTGACA | 4067 |
rs34638311 | in-del | -/C | | | intron-variant | LYN | GRCh38.p7 | 8:55985460 | ATAGCAAATCTGTTT[-/C]CAGGTATATTTGGAA | 4067 |
rs34638865 | in-del | -/T | | | intron-variant | LYN | GRCh38.p7 | 8:55894007 | ACACAAGATATGAAG[-/T]AACATGCACAGGCAC | 4067 |
rs34693080 | in-del | -/G | | | intron-variant | LYN | GRCh38.p7 | 8:55889195 | ATTTTTTTGTTTTTT[-/G]GGGAGGCCAAGGCAG | 4067 |
rs34706733 | in-del | -/A | | | intron-variant | LYN | GRCh38.p7 | 8:55890117 | CCTGCCTCTATAGAC[-/A]AAAAAAAAAAAAAAA | 4067 |
rs34759580 | in-del | -/G | | | intron-variant | LYN | GRCh38.p7 | 8:55882798 | ACAGAAAAAGATTCA[-/G]GGGGGTTGTCTAAGG | 4067 |
rs34774022 | in-del | -/C | | | intron-variant | LYN | GRCh38.p7 | 8:55903897 | GCATGGCCCTGTAGT[-/C]CCCAGCTAGCTACTT | 4067 |
rs34824007 | snp | A/C | 0.268995 | 0.249277 | intron-variant | LYN | GRCh38.p7 | 8:55886384 | AGCTGGGATTACAGG[A/C]ATGCACCAATGCACC | 4067 |
rs34839284 | in-del | -/T | 0.483272 | 0.0899109 | intron-variant | LYN | GRCh38.p7 | 8:55886241 | TGGCTGTCAAACATC[-/T]TTTTTTTTTTTTTTT | 4067 |
rs34845241 | in-del | -/T | | | intron-variant | LYN | GRCh38.p7 | 8:55973228 | GTGCACGTGACAGCC[-/T]TCACAGTTCATGTGA | 4067 |
rs34851223 | in-del | -/A | | | utr-variant-5-prime | LYN | GRCh38.p7 | 8:55877666 | AAATATGATATCTGC[-/A]AAAATGAGGATACAC | 4067 |
rs34910040 | in-del | -/T/TT | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55894388 | AATTTTTTTTTTTTT[-/T/TT]GAGACAGTGGTCACT | 4067 |
rs34955873 | snp | A/C | 0.25214 | 0.249991 | intron-variant | LYN | GRCh38.p7 | 8:55965029 | CTATTACTCCCTTCT[A/C]CCCATTTTTTTTTTA | 4067 |
rs34962100 | in-del | -/G | | | intron-variant | LYN | GRCh38.p7 | 8:55961714 | TGGCAAAAGGGAAAT[-/G]GGTTTTGTTTCTTTA | 4067 |
rs35015766 | snp | C/T | 0.393065 | 0.205018 | intron-variant | LYN | GRCh38.p7 | 8:55911055 | GCGCCCACCTCCATG[C/T]CCGGCTAATTTATAT | 4067 |
rs35072619 | in-del | -/G | | | intron-variant | LYN | GRCh38.p7 | 8:55916702 | CTCTGGCTCCATACT[-/G]GGAAATGTGTGTGGC | 4067 |
rs35099896 | in-del | -/C | | | intron-variant | LYN | GRCh38.p7 | 8:55972695 | AAATCTATCACTTTT[-/C]CCATAGTGCATAACA | 4067 |
rs35106280 | in-del | -/C | | | intron-variant | LYN | GRCh38.p7 | 8:55908035 | GAAACTCCAACAGTT[-/C]CTAATGAATAAAGAG | 4067 |
rs35110576 | in-del | -/C | | | intron-variant | LYN | GRCh38.p7 | 8:55955987 | TATGAATGTTCACAT[-/C]ACAAATTATTATGTG | 4067 |
rs35194992 | in-del | -/A | | | intron-variant | LYN | GRCh38.p7 | 8:55970477 | TTCATTGTGTCCATT[-/A]AGTAATGTTCAGCAG | 4067 |
rs35305537 | in-del | -/A | | | intron-variant | LYN | GRCh38.p7 | 8:55977752 | ACTCCTATCTCTACC[-/A]AAAAAAAAAAAAAAA | 4067 |
rs35316542 | in-del | -/C | | | intron-variant | LYN | GRCh38.p7 | 8:55920778 | CCCCCCCTTGCCCTT[-/C]CCCCACCACCCCCCC | 4067 |
rs35334572 | in-del | -/G | | | intron-variant | LYN | GRCh38.p7 | 8:55997900 | CATCCTGGCTAACAT[-/G]GGTGAAACCCCGTCT | 4067 |
rs35380752 | snp | C/T | 0.264632 | 0.249571 | intron-variant | LYN | GRCh38.p7 | 8:55936375 | CTGGGCGTGGTGGCT[C/T]ATTCCTATAATCCCA | 4067 |
rs35393123 | in-del | -/A | | | intron-variant | LYN | GRCh38.p7 | 8:55915542 | AACCCCGTCTCTACT[-/A]AAAAATACAAAAAAT | 4067 |
rs35418432 | in-del | -/T | | | intron-variant | LYN | GRCh38.p7 | 8:55950446 | TCTTTTTGATGTGTA[-/T]TTTCTATTCTAGGCA | 4067 |
rs35488882 | in-del | -/TA | | | intron-variant | LYN | GRCh38.p7 | 8:55942443 | ATATGTGTGTGTGTG[-/TA]TATATATATATATAT | 4067 |
rs35513906 | in-del | -/G | | | intron-variant | LYN | GRCh38.p7 | 8:55958621 | TCTTTAACACCAACT[-/G]CCCTGATCCCCTCTC | 4067 |
rs35559279 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LYN | GRCh38.p7 | 8:55977100 | TTAGGCAGGAGAATC[A/G]CTTGAACCCAGAAGG | 4067 |
rs35631616 | in-del | -/T | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55967309 | AATTCCTCTTTCATT[-/T]TTTTTTTTTTTTTTT | 4067 |
rs35663372 | in-del | -/A | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55919022 | AGACCCTGTCTCTAC[-/A]AAAAAAAAAAAAAAA | 4067 |
rs35692636 | snp | G/T | | | intron-variant | LYN | GRCh38.p7 | 8:55957586 | GAGAGACAAGTAAAG[G/T]GAACAAAGTAATTCA | 4067 |
rs35717306 | in-del | -/A | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55976335 | GCAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 4067 |
rs35748944 | in-del | -/C | | | intron-variant | LYN | GRCh38.p7 | 8:55920717 | ACTCTGTTGCCCAGG[-/C]TGGAGGGCAGTGGCA | 4067 |
rs35756022 | snp | C/G | 0.495407 | 0.0477027 | upstream-variant-2KB | LYN | GRCh38.p7 | 8:55876567 | GATTTAACTGGTCTA[C/G]GTAGGGCCTGGGCAT | 4067 |
rs35762009 | in-del | -/C | | | intron-variant | LYN | GRCh38.p7 | 8:56009902 | TTTTGTTTTTTTCCA[-/C]CCTAGGGAGAACTAA | 4067 |
rs35771157 | in-del | -/C | | | intron-variant | LYN | GRCh38.p7 | 8:56000930 | GGTATCTGCCCATGT[-/C]CCTTGAGAGTGAATA | 4067 |
rs35790880 | in-del | -/A | | | intron-variant | LYN | GRCh38.p7 | 8:55932749 | TTGATAAGAATTATT[-/A]ATACTCGCATTTATA | 4067 |
rs35814597 | in-del | -/A | | | intron-variant | LYN | GRCh38.p7 | 8:55964898 | ATACTCTTGCACCCT[-/A]AAAAGGGGACCGTCC | 4067 |
rs35829952 | snp | A/G | 0.44651 | 0.154543 | intron-variant | LYN | GRCh38.p7 | 8:55976304 | TACATTCCAGCCTGA[A/G]TGACAGAGCAAGACT | 4067 |
rs35835891 | in-del | -/T | | | intron-variant | LYN | GRCh38.p7 | 8:55974403 | AAATTTAAAGCCACA[-/T]TTTTAAGGTGGAAAT | 4067 |
rs35854565 | in-del | -/G | | | intron-variant | LYN | GRCh38.p7 | 8:55931893 | TTTTAATGTGCTTTT[-/G]GCTAGTTCTTCAAAT | 4067 |
rs35860381 | snp | G/T | | | upstream-variant-2KB | LYN | GRCh38.p7 | 8:55877282 | TTAATTTTTTTATTG[G/T]GGGGGGGGTCTCACG | 4067 |
rs35868178 | in-del | -/G | | | intron-variant | LYN | GRCh38.p7 | 8:55888548 | ATGCTTTGAGTAGGT[-/G]GGAGAGTTGAATGAC | 4067 |
rs35908383 | in-del | -/G | | | intron-variant | LYN | GRCh38.p7 | 8:55983125 | CTTTCTGCATTTCCA[-/G]GTTCAAGAGCACCAG | 4067 |
rs35929723 | in-del | -/A | | | intron-variant | LYN | GRCh38.p7 | 8:55915383 | TGTGAAACCAGAACC[-/A]AACAAAGAAGTATTT | 4067 |
rs35946646 | in-del | -/TA | | | intron-variant | LYN | GRCh38.p7 | 8:55942395 | GTATATATATATGTG[-/TA]TATATATGTGTATAT | 4067 |
rs35994270 | in-del | -/A | 0.487809 | 0.0771174 | intron-variant | LYN | GRCh38.p7 | 8:55902604 | CAATATATAGCATAC[-/A]AAAAAAAAACAACAA | 4067 |
rs36039039 | in-del | -/C | | | intron-variant | LYN | GRCh38.p7 | 8:55951322 | CTTACCAGGCTTTGT[-/C]TTGCTGAGCCTTTTG | 4067 |
rs36045527 | in-del | -/T | | | intron-variant | LYN | GRCh38.p7 | 8:55982690 | GTCATCATTCCATCA[-/T]TTTGTAGCCATCCCC | 4067 |
rs36052560 | in-del | -/G | | | intron-variant | LYN | GRCh38.p7 | 8:55950135 | GAGTAATACTCCACT[-/G]GGATGGATATTCCAG | 4067 |
rs36090684 | in-del | -/A | | | intron-variant | LYN | GRCh38.p7 | 8:55995194 | CACTGCCTGCTGTTT[-/A]CTGGGCAGCAGAGGC | 4067 |
rs41429544 | snp | C/T | 0.105924 | 0.204309 | intron-variant | LYN | GRCh38.p7 | 8:55906192 | TTTCACAACCAACCC[C/T]GATTAAATCCTGATC | 4067 |
rs45489500 | snp | A/G | 0.0111196 | 0.0737302 | utr-variant-3-prime | LYN | GRCh38.p7 | 8:56010483 | TTGCAATGAATCCCC[A/G]ATAATTGCAGAACTA | 4067 |
rs45587541 | snp | A/G | | | missense | LYN | GRCh38.p7 | 8:55966723 | TTCCTAGGTTACTAT[A/G]ACAACAGTACCAAGG | 4067 |
rs55703704 | snp | C/T | 0.135143 | 0.222054 | utr-variant-3-prime | LYN | GRCh38.p7 | 8:56011586 | TCCGTTTATGGGGGC[C/T]AGATAGAATTTGTTT | 4067 |
rs55781514 | in-del | -/A | | | intron-variant | LYN | GRCh38.p7 | 8:55909047 | CACACACACACACAC[-/A]CACACCCCACATTTT | 4067 |
rs55803865 | snp | A/C/T | 0.000131876 | 0.00811915 | stop-gained, synonymous-codon | LYN | GRCh38.p7 | 8:55966842 | GCTCGTGAGGCTCTA[A/C/T]GCTGTGGTCACCAGG | 4067 |
rs55833123 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | LYN | GRCh38.p7 | 8:55920853 | AGGCATGTGCTACCA[C/T]GCCTGGCTAATTTTT | 4067 |
rs55891909 | snp | C/T | 0.281841 | 0.247964 | intron-variant | LYN | GRCh38.p7 | 8:55967224 | GGAATTTTTGAAATA[C/T]ATATGCTTAAAATGT | 4067 |
rs55893564 | snp | C/T | 0.0836354 | 0.186609 | intron-variant | LYN | GRCh38.p7 | 8:55947554 | ATCCTTTGTGCCCCA[C/T]GAGGTTTGTTAAAAC | 4067 |
rs55895527 | snp | A/G | | | intron-variant | LYN | GRCh38.p7 | 8:55911083 | TATATATATACATAC[A/G]TATATATATATATAT | 4067 |
rs55914142 | snp | C/T | | | intron-variant | LYN | GRCh38.p7 | 8:55911104 | ATATATATATACATA[C/T]ACGTATATATACGTA | 4067 |
rs55989796 | in-del | -/CA | | | intron-variant | LYN | GRCh38.p7 | 8:55911078 | ATTTATATATATATA[-/CA]TACATATATATATAT | 4067 |
rs55992019 | snp | A/G | | | intron-variant | LYN | GRCh38.p7 | 8:55942395 | TGTATATATATATGT[A/G]TATATATGTGTATAT | 4067 |
rs56007716 | snp | C/T | 0.327211 | 0.237778 | intron-variant | LYN | GRCh38.p7 | 8:55953401 | ACCTGTAATCCAGCA[C/T]TTTGGGAGGCCGAGG | 4067 |
rs56020575 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | LYN | GRCh38.p7 | 8:55920543 | TGGAGGACTGTTATC[C/T]ACCCTTCACAGATGA | 4067 |
rs56027679 | snp | C/T | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55911078 | ATTTATATATATATA[C/T]ATACATATATATATA | 4067 |
rs56050111 | snp | C/G | 0.0980852 | 0.198549 | intron-variant | LYN | GRCh38.p7 | 8:55994086 | GCTGTTTGAAATAGA[C/G]CTGGATTTACTTAGC | 4067 |
rs56094668 | snp | A/G | 3.31285e-05 | 0.00406978 | intron-variant, synonymous-codon | LYN | GRCh38.p7 | 8:55941970 | TGTGAGAGATCCAAC[A/G]TCCAATAAACAGCAA | 4067 |
rs56103677 | snp | C/T | 0.197703 | 0.244469 | intron-variant | LYN | GRCh38.p7 | 8:55936306 | ATGGATCTGGAGCTT[C/T]CTCCACAGAAAGGCA | 4067 |
rs56119798 | snp | A/G | 0.198324 | 0.244601 | intron-variant | LYN | GRCh38.p7 | 8:55936409 | CTTTGGGAGGCTCAC[A/G]TGGGAGGATCACCTG | 4067 |
rs56120708 | snp | A/C | 0.18134 | 0.240387 | intron-variant | LYN | GRCh38.p7 | 8:55921053 | GAATGATCACAGATT[A/C]TCAGATAATGGGGGA | 4067 |
rs56136409 | snp | C/G/T | 0.128748 | 0.225501 | intron-variant | LYN | GRCh38.p7 | 8:55924552 | TATTTTTAGTAGAAA[C/G/T]GGGGTTTCACCATGT | 4067 |
rs56143558 | in-del | -/TTAAA | | | intron-variant | LYN | GRCh38.p7 | 8:56002652 | TTAAATTAAATTAAA[-/TTAAA]AAATAAAAAGAGAAC | 4067 |
rs56150342 | snp | A/G | 0.142609 | 0.225759 | intron-variant | LYN | GRCh38.p7 | 8:55929556 | CAGAAAATATCAATA[A/G]TTGAGTTATTACCAG | 4067 |
rs56181546 | snp | A/G | 0.314301 | 0.241589 | intron-variant | LYN | GRCh38.p7 | 8:55955506 | CCTCCTCATTTCTCT[A/G]TGTGCTCTTTTTTTA | 4067 |
rs56267723 | snp | A/G | | | intron-variant | LYN | GRCh38.p7 | 8:55942393 | TGTGTATATATATAT[A/G]TGTATATATGTGTAT | 4067 |
rs56299473 | snp | C/T | | | intron-variant | LYN | GRCh38.p7 | 8:55994096 | ATAGAGCTGGATTTA[C/T]TTAGCCGTAGTAAAT | 4067 |
rs56300145 | snp | A/C | 0.141934 | 0.225437 | intron-variant | LYN | GRCh38.p7 | 8:55953670 | AGAAAAACAAAAAAA[A/C]CCCACAAATTTCAAA | 4067 |
rs56328126 | snp | C/T | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55911098 | ATATATATATATATA[C/T]ACATACACGTATATA | 4067 |
rs56329099 | snp | A/T | 0.143284 | 0.226079 | intron-variant | LYN | GRCh38.p7 | 8:55931719 | AAATTTAATAGTCAC[A/T]TAGTATTCTTTTGTG | 4067 |
rs56337639 | snp | A/G | 0.116838 | 0.211584 | intron-variant | LYN | GRCh38.p7 | 8:55957187 | AGTGGACAAACTCCA[A/G]TCTTCAGTTGTTCAA | 4067 |
rs56354651 | snp | C/T | 0.000724864 | 0.0190238 | synonymous-codon | LYN | GRCh38.p7 | 8:56009990 | CCCAGATGAGCTCTA[C/T]GACATTATGAAAATG | 4067 |
rs56368841 | snp | C/T | | | intron-variant | LYN | GRCh38.p7 | 8:55911100 | ATATATATATATATA[C/T]ATACACGTATATATA | 4067 |
rs56399348 | snp | G/T | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55911090 | ATACATACATATATA[G/T]ATATATATACATACA | 4067 |
rs56735298 | snp | A/G | 0.197703 | 0.244469 | intron-variant | LYN | GRCh38.p7 | 8:55935593 | AGCCTGGCCAACATG[A/G]TGAAACCCTGTCTGT | 4067 |
rs56745122 | snp | G/T | 0.206642 | 0.246211 | intron-variant | LYN | GRCh38.p7 | 8:55953374 | AATTTCAGGCCGGGC[G/T]TGGTGGCTCACACCT | 4067 |
rs56890176 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | LYN | GRCh38.p7 | 8:55977431 | CTCTGTTCTCCCCCA[A/G]CACACCAGGGTGTTC | 4067 |
rs56923750 | in-del | -/TTTTT | | | intron-variant | LYN | GRCh38.p7 | 8:55910006 | GTCTTTTTTTTTTTT[-/TTTTT]GAGTTGTTTGAGTTT | 4067 |
rs57006402 | snp | A/G | 0.376394 | 0.215696 | intron-variant | LYN | GRCh38.p7 | 8:55946329 | GCTCCTGTTCTTTCT[A/G]ACTTAATAAATGAGC | 4067 |
rs57036917 | snp | A/G | | | intron-variant | LYN | GRCh38.p7 | 8:55990812 | TTTCAGGTTTCTTTG[A/G]AATCCCCTGGGCCAA | 4067 |
rs57095067 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | LYN | GRCh38.p7 | 8:56000115 | ATACTAGAATGTTCC[A/G]GGCATGGTTGTTGGT | 4067 |
rs57109999 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | LYN | GRCh38.p7 | 8:55905102 | TATGTGGGAATCTTT[C/G]GGCTATTTTAGAAAA | 4067 |
rs57170159 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | LYN | GRCh38.p7 | 8:55997851 | GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCAC | 4067 |
rs57171753 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | LYN | GRCh38.p7 | 8:55920855 | GCATGTGCTACCACG[C/T]CTGGCTAATTTTTGT | 4067 |
rs57239591 | in-del | -/GTTT | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55932428 | TTTGTTTGTTTGTTT[-/GTTT]TTGTTTTTTTTTAGA | 4067 |
rs57309959 | snp | A/G | | | intron-variant | LYN | GRCh38.p7 | 8:55911117 | TACACGTATATATAC[A/G]TATATATATACACAT | 4067 |
rs57325128 | snp | C/G/T | 0.0138799 | 0.0821421 | intron-variant | LYN | GRCh38.p7 | 8:55905082 | ATCATTTTACTAGAT[C/G/T]CAGCTATGTGGGAAT | 4067 |
rs57357972 | snp | C/G | 0.0387552 | 0.1337 | intron-variant | LYN | GRCh38.p7 | 8:55881575 | TAGAGTCTTTGGTGA[C/G]TGGGCCTCTTTGGAT | 4067 |
rs57379839 | snp | C/G | 0.395087 | 0.203592 | intron-variant | LYN | GRCh38.p7 | 8:55986193 | ACCAGAATCCCCCCC[C/G]CAAAAAAAAACGCTA | 4067 |
rs57413136 | in-del | -/GT | | | intron-variant | LYN | GRCh38.p7 | 8:55988328 | TGTGTGTGTGTGTGT[-/GT]TTACATCCTATTTTT | 4067 |
rs57500802 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | LYN | GRCh38.p7 | 8:55996578 | CCCTCCTTTCCTCCT[C/G]TCTCCTTGTTTCCTT | 4067 |
rs57505087 | snp | C/T | 0.030665 | 0.119967 | intron-variant | LYN | GRCh38.p7 | 8:55933708 | CTGTCTCATTATCCT[C/T]TTTGCACTCCCTTCC | 4067 |
rs57555655 | in-del | -/A/AAA | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55890138 | AAAAAAAAAAAAAAA[-/A/AAA]GAATAAATAAAAACA | 4067 |
rs57735433 | snp | A/G | 0.123798 | 0.215808 | intron-variant | LYN | GRCh38.p7 | 8:55896748 | CACGTTTATTTATTT[A/G]TTTATTTAGAGACAG | 4067 |
rs57813383 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | LYN | GRCh38.p7 | 8:55952981 | GTTGTTGCCCCGGCT[C/T]CTTTCTATGACCTGC | 4067 |
rs57862713 | in-del | -/T | | | intron-variant | LYN | GRCh38.p7 | 8:55920688 | AGGAAATTTTTTTTT[-/T]GAGACAGTATCTCAC | 4067 |
rs57977675 | snp | A/G | 0.021333 | 0.101051 | intron-variant | LYN | GRCh38.p7 | 8:55959032 | TTTGGAGGAACTGCC[A/G]TACTGTTTTCTACTT | 4067 |
rs57986222 | snp | A/G | 0.146985 | 0.227789 | intron-variant | LYN | GRCh38.p7 | 8:55951214 | CGCCACTGCACTCTA[A/G]CTAGCCTGAGTGACA | 4067 |
rs58038386 | snp | C/T | | | intron-variant | LYN | GRCh38.p7 | 8:55897844 | CTTGAGCCTGAGAGG[C/T]GGAGGCTGCAGTGAG | 4067 |
rs58096764 | snp | C/T | 0.258843 | 0.249844 | utr-variant-3-prime, downstream-variant-500B | LYN | GRCh38.p7 | 8:56012205 | AGCACACACAGTCTC[C/T]TTACTTAGCTATAGG | 4067 |
rs58233309 | in-del | -/AA | | | intron-variant | LYN | GRCh38.p7 | 8:55887560 | ATAAAAATATAAATA[-/AA]TATATATATATATAT | 4067 |
rs58293361 | in-del | -/T | | | intron-variant | LYN | GRCh38.p7 | 8:55924372 | CCTCATTTTTTTTTT[-/T]CTTTTTTTGAGATGG | 4067 |
rs58452244 | snp | C/G | | | intron-variant | LYN | GRCh38.p7 | 8:55928344 | AGAGATGGGGTTTCA[C/G]CATGTTGGCCAGGCT | 4067 |
rs58506995 | snp | A/G | 0.330249 | 0.23677 | intron-variant, upstream-variant-2KB | LYN | GRCh38.p7 | 8:55923114 | GCCTCGGGTGACTGG[A/G]ATGGTGAGAAAAAAC | 4067 |
rs58515933 | snp | A/G | | | intron-variant | LYN | GRCh38.p7 | 8:55906647 | CAGGCGTGAGCCATC[A/G]CGCCTGGCCGAGGTC | 4067 |
rs58547202 | snp | A/G | 0.0744748 | 0.178019 | intron-variant | LYN | GRCh38.p7 | 8:55954455 | TTCTTAACATTAAGT[A/G]TTGCCTTCTCAGGCT | 4067 |
rs58579760 | snp | C/T | | | intron-variant | LYN | GRCh38.p7 | 8:55897860 | GGAGGCTGCAGTGAG[C/T]CGAGATCGCGCCACT | 4067 |
rs58704162 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | LYN | GRCh38.p7 | 8:56000579 | TAAAAATACAAAAAA[C/T]TAGCTGGGCGTAGTG | 4067 |
rs58841833 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | LYN | GRCh38.p7 | 8:55905273 | AAAAATTAGCCAGGC[A/G]TGGTGGCAGGCACCT | 4067 |
rs58849019 | snp | A/T | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55996474 | CATTCCTGTGTGAAA[A/T]ATTCGAATCAGAGTT | 4067 |
rs58873125 | in-del | -/T | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55886258 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCGC | 4067 |
rs58976187 | snp | G/T | | | intron-variant | LYN | GRCh38.p7 | 8:55897837 | AGGATTGCTTGAGCC[G/T]GAGAGGTGGAGGCTG | 4067 |
rs59386465 | in-del | -/T | 0.418007 | 0.185132 | intron-variant | LYN | GRCh38.p7 | 8:55894376 | GATTAACTTTCTTAA[-/T]TTTTTTTTTTTTGAG | 4067 |
rs59414068 | snp | C/T | 0.0748431 | 0.178382 | intron-variant, downstream-variant-500B | LYN | GRCh38.p7 | 8:55968380 | CCTGCCTCAGCCTCC[C/T]AAGTAGCTGGGATTA | 4067 |
rs59446152 | snp | G/T | | | intron-variant | LYN | GRCh38.p7 | 8:55932717 | TGAGCCACCACACCA[G/T]GCCTAAAACAATTAT | 4067 |
rs59462684 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | LYN | GRCh38.p7 | 8:55999840 | GCCAGGCATGGTGAC[A/G]CATGCCTGTAATCCC | 4067 |
rs59511264 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | LYN | GRCh38.p7 | 8:56004241 | CCGGCCTAAATATTT[C/T]ATTCTTATCTAAGTA | 4067 |
rs59615698 | snp | C/T | | | intron-variant | LYN | GRCh38.p7 | 8:55897850 | CCTGAGAGGTGGAGG[C/T]TGCAGTGAGTCGAGA | 4067 |
rs59717853 | snp | A/G | 0.397633 | 0.201754 | intron-variant | LYN | GRCh38.p7 | 8:55899065 | CAGGCATGAGACACT[A/G]TACCCAGCTAAGTTT | 4067 |
rs59739013 | in-del | -/CACACACACACACACACACA/CATA | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55887604 | ACACACACACACACA[-/CACACACACACACACACACA/CATA]TATATATATATTTTT | 4067 |
rs59848254 | in-del | -/AA | | | intron-variant | LYN | GRCh38.p7 | 8:55935797 | AAAAAAAAAAAAAAA[-/AA]CAGGAATTTGGGAAA | 4067 |
rs59972583 | snp | A/G/T | | | intron-variant | LYN | GRCh38.p7 | 8:55990811 | TTTTCAGGTTTCTTT[A/G/T]AAATCCCCTGGGCCA | 4067 |
rs60016461 | snp | C/G | 0.0520825 | 0.152737 | intron-variant | LYN | GRCh38.p7 | 8:55958570 | CAACCAATCTCCAGA[C/G]TCTCTTTTCATCTGA | 4067 |
rs60087681 | snp | A/G | 0.0792508 | 0.182605 | intron-variant | LYN | GRCh38.p7 | 8:55920697 | TTTTTTTGAGACAGT[A/G]TCTCACTCTGTTGCC | 4067 |
rs60165767 | snp | C/T | 0.0543475 | 0.155628 | intron-variant | LYN | GRCh38.p7 | 8:55907552 | CTTTACCTTTCATTG[C/T]AGGTGCTTTTTTTTT | 4067 |
rs60176166 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | LYN | GRCh38.p7 | 8:55975566 | CTCTAAATAAGGGAA[C/T]ACAAATATATCACTT | 4067 |
rs60186504 | snp | A/C | 0.0744748 | 0.178019 | intron-variant | LYN | GRCh38.p7 | 8:55974061 | CCCAACAGCCTTGAA[A/C]GCATATATTTTGTTG | 4067 |
rs60508113 | snp | A/G | 0.194278 | 0.243711 | intron-variant | LYN | GRCh38.p7 | 8:55937570 | TGTATTTAAAGAACA[A/G]ATTTCAAGAAGTGGA | 4067 |
rs60513869 | in-del | -/T | 0.474 | 0.111014 | intron-variant | LYN | GRCh38.p7 | 8:55898992 | ACTGTGCTGGGCTAA[-/T]TTTTTTTATTTTTTG | 4067 |
rs60741728 | snp | A/G | 0.0799831 | 0.183287 | intron-variant, upstream-variant-2KB | LYN | GRCh38.p7 | 8:55923137 | GAAAAAACAATTTTC[A/G]GTAAGGAAGATGGAA | 4067 |
rs60805166 | snp | G/T | 0.0517044 | 0.152246 | intron-variant | LYN | GRCh38.p7 | 8:55962362 | AGATGCATCTGTGCT[G/T]TTGCGTGTGGCTACA | 4067 |
rs60826707 | snp | A/T | 0.0520825 | 0.152737 | intron-variant | LYN | GRCh38.p7 | 8:55958912 | GTGAATTTGCCACTG[A/T]GAACATGGGTGCACA | 4067 |
rs60930363 | in-del | -/ATTT/ATTTATTTATTTATTT | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55908222 | TTTATTTATTTATTT[-/ATTT/ATTTATTTATTTATTT]GAGACAGAGTCTCAC | 4067 |
rs60970769 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | LYN | GRCh38.p7 | 8:55988605 | GTCTACTAAAACAGG[C/T]AAAGCACCAGGAAAA | 4067 |
rs61007770 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | LYN | GRCh38.p7 | 8:55988619 | GTAAAGCACCAGGAA[A/G]ATCAGATCTTCATTT | 4067 |
rs61067915 | snp | A/G | | | intron-variant | LYN | GRCh38.p7 | 8:55897834 | GGGAGGATTGCTTGA[A/G]CCTGAGAGGTGGAGG | 4067 |
rs61308942 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | LYN | GRCh38.p7 | 8:55987003 | TTACAGGTGGGAGCC[A/G]CCACATTCGGCCTAA | 4067 |
rs61391341 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | LYN | GRCh38.p7 | 8:55999738 | GCACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC | 4067 |
rs61446372 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | LYN | GRCh38.p7 | 8:55904296 | TAACTCAATTATTTG[A/G]CTGTCGGGTTGATGG | 4067 |
rs61480621 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | LYN | GRCh38.p7 | 8:55903068 | CGGCCAGGCTGGTCT[C/T]GAACTCCTGACTTCG | 4067 |
rs61539692 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | LYN | GRCh38.p7 | 8:55910936 | GAGTCTCGCTCTGAC[A/G]CCCAGGCTGGAGTGC | 4067 |
rs62515360 | snp | C/T | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55909477 | CCATTGGCTCCTCAG[C/T]ACATTTTCTTTATCT | 4067 |
rs62515361 | snp | C/T | | | intron-variant | LYN | GRCh38.p7 | 8:55911246 | ATACATATATATATA[C/T]GTGTGTGTGTGTATA | 4067 |
rs62515362 | snp | A/G | | | intron-variant | LYN | GRCh38.p7 | 8:55911247 | TACATATATATATAC[A/G]TGTGTGTGTGTATAT | 4067 |
rs62515363 | snp | A/G | | | intron-variant | LYN | GRCh38.p7 | 8:55911249 | CATATATATATACGT[A/G]TGTGTGTGTATATAT | 4067 |
rs62515364 | snp | A/G | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55911263 | TGTGTGTGTGTATAT[A/G]TATATATATATATAT | 4067 |
rs62515365 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | LYN | GRCh38.p7 | 8:55918184 | TCTGGCTCAGACAGG[A/G]CACTTTGTGTGGCTG | 4067 |
rs62515366 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | LYN | GRCh38.p7 | 8:55927572 | AGGTGCGGTGGTTCA[C/T]GTCTGTAATCCCAGC | 4067 |
rs62515367 | snp | C/T | 0.234109 | 0.249494 | intron-variant | LYN | GRCh38.p7 | 8:55928388 | TGACCTCAGGTGATC[C/T]GCCGACCTTGGCCTC | 4067 |
rs62515384 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYN | GRCh38.p7 | 8:55930512 | CTCTGCTTTGAATGT[A/C]CCCTTCTGGTCCTTT | 4067 |
rs62515386 | snp | A/C | 0.0752113 | 0.178743 | intron-variant | LYN | GRCh38.p7 | 8:55945715 | TCTGTGCCACCAAAT[A/C]CTTCCCAATAACTCA | 4067 |
rs62515387 | snp | A/T | | | intron-variant | LYN | GRCh38.p7 | 8:55952412 | AGAAAAAAAAAAAAT[A/T]AGCCAGGCATAGTGG | 4067 |
rs62515388 | snp | A/G | 0.212122 | 0.247114 | intron-variant | LYN | GRCh38.p7 | 8:55972343 | CCTCAAGGTGGCGCT[A/G]GTGAGACCACCTGGT | 4067 |
rs62515390 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYN | GRCh38.p7 | 8:55985371 | GCCACAGAGAGCAGA[C/T]GTCACAGGCTTCCCT | 4067 |
rs62515391 | snp | A/G | | | intron-variant | LYN | GRCh38.p7 | 8:55998286 | TTTCCGGTTTTCCTT[A/G]ATGGCACTTTCCAGT | 4067 |
rs62515392 | snp | A/G | 0.5 | 0 | missense | LYN | GRCh38.p7 | 8:56010063 | TTACAGAGCGTCCTG[A/G]ATGATTTCTACACAG | 4067 |
rs62516880 | snp | C/T | 0.162581 | 0.234218 | upstream-variant-2KB | LYN | GRCh38.p7 | 8:55876849 | ATGAGATGATGATGG[C/T]GGTGCTAATGAAGAA | 4067 |
rs62516882 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | LYN | GRCh38.p7 | 8:55895626 | GAGACCTCATCTCTA[C/T]AATTTTTTTTTTAAA | 4067 |
rs62516893 | snp | G/T | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55902867 | GGCTTTTTTTTTTTG[G/T]AGACGGAGTCTCTCT | 4067 |
rs62516894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYN | GRCh38.p7 | 8:55904185 | CTGAAATAAGTACGA[C/T]GAACAATTTTTTAAA | 4067 |
rs66476461 | snp | C/G | 0.302686 | 0.244385 | intron-variant | LYN | GRCh38.p7 | 8:55948663 | CAAATAGGGTTTGAG[C/G]GGGAGACTCCCTTAT | 4067 |
rs66520008 | in-del | -/C/CC | 0.300169 | 0.244914 | intron-variant | LYN | GRCh38.p7 | 8:55986185 | AAAATCCACCAGAAT[-/C/CC]CCCCCCCGCAAAAAA | 4067 |
rs66536728 | in-del | -/T | 0.481396 | 0.0946345 | intron-variant | LYN | GRCh38.p7 | 8:55887615 | ACACATATATATATA[-/T]TTTTTTTTTCCTGAG | 4067 |
rs66667320 | multinucleotide-polymorphism | AG/TT | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55910171 | TCTCATTTGTCTACT[AG/TT]TGTTTTTGTTGCCTG | 4067 |
rs66726290 | snp | C/G | 0.198014 | 0.244535 | intron-variant | LYN | GRCh38.p7 | 8:55936958 | AAAGTAGGCACATAC[C/G]TGTTTATCCCTTTTC | 4067 |
rs66838044 | snp | A/G | 0.184838 | 0.241358 | intron-variant | LYN | GRCh38.p7 | 8:55960413 | AGAAGAGAAAAAAAT[A/G]GAAAATTTTGACTTG | 4067 |
rs66871317 | snp | A/C | 0.373598 | 0.21731 | intron-variant | LYN | GRCh38.p7 | 8:55912738 | TCTGAAAAAAAAAAA[A/C]AAAACAAAACAAAAC | 4067 |
rs66913087 | snp | C/T | 0.212728 | 0.247206 | intron-variant | LYN | GRCh38.p7 | 8:55950387 | CATATTTATGGGATA[C/T]CTGTGATATTTTGAT | 4067 |
rs67222355 | snp | C/T | 0.329783 | 0.236927 | intron-variant | LYN | GRCh38.p7 | 8:55928260 | AAGTGATTCTCATGC[C/T]TCACCCTCTGGAGTA | 4067 |
rs67432274 | snp | A/G | 0.277067 | 0.24853 | intron-variant | LYN | GRCh38.p7 | 8:55926378 | GTTGACTATGCATGT[A/G]TAGATGTGTAAGTTC | 4067 |
rs67767278 | in-del | -/TTTG | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55932425 | TTTTTTGTTTGTTTG[-/TTTG]TTTTTGTTTTTTTTT | 4067 |
rs67769144 | snp | C/T | 0.17654 | 0.238964 | intron-variant | LYN | GRCh38.p7 | 8:55990454 | AAGGTGTCAGTTAAA[C/T]CTCTCCTGGATCAGG | 4067 |
rs68079292 | in-del | -/GC | 0.421842 | 0.181577 | intron-variant | LYN | GRCh38.p7 | 8:55911681 | GCAGTCCTATGAGCT[-/GC]GGGGCACCTGCCCTG | 4067 |
rs71213348 | snp | A/G | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55911231 | TGTGTGTGTGTGTGT[A/G]TATATATATATATAC | 4067 |
rs71256582 | in-del | -/TT | 0.336474 | 0.234568 | intron-variant | LYN | GRCh38.p7 | 8:55890728 | ATATGTACATTGGAA[-/TT]TTTTTTTTTTTTTTT | 4067 |
rs71256584 | in-del | -/ACGTGTGTGTGTGTGTGTGTATATATATATATACGTGTGTGTATATGTATATAT | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55911270 | TGTATATATATATAT[lengthTooLong]ATATATATATATATA | 4067 |
rs71256586 | in-del | -/GT/GTGT/GTGTGT | | | intron-variant | LYN | GRCh38.p7 | 8:55988291 | TGTGTGTGTGTGTGT[-/GT/GTGT/GTGTGT]TTACATCCTATTTTT | 4067 |
rs71501591 | multinucleotide-polymorphism | CA/TG | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55886303 | TGTAGTACAATGGTG[CA/TG]ATCTCCACTCACTGC | 4067 |
rs71501592 | multinucleotide-polymorphism | CGT/TAC | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55911187 | GTGTATATATATATA[CGT/TAC]GTGTGTGTGTGTATA | 4067 |
rs71513431 | snp | A/G | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55911175 | TATATATATATACGT[A/G]TATATATATATACGT | 4067 |
rs71513432 | snp | C/T | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55911178 | ATATATATACGTGTA[C/T]ATATATATACGTGTG | 4067 |
rs71517988 | multinucleotide-polymorphism | ACTCACTGCAA/GCTCACTGCAG | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55908315 | AGTGGTGCAATCTCG[ACTCACTGCAA/GCTCACTGCAG]CCTCCGCCTCCCAGG | 4067 |
rs71517989 | in-del | ACCCAT/CCCCA | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55965029 | CTATTACTCCCTTCT[ACCCAT/CCCCA]TTTTTTTTTTAACAT | 4067 |
rs71519439 | snp | C/T | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55887605 | ACACACACACACACA[C/T]ATATATATATTTTTT | 4067 |
rs71519440 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | LYN | GRCh38.p7 | 8:55899457 | CAAGCAGACTTTATA[A/C]ATTAACATAAATGTA | 4067 |
rs71519441 | snp | A/C/G | 0.0182361 | 0.0940017 | intron-variant | LYN | GRCh38.p7 | 8:55911570 | AAATGTACATTCACT[A/C/G]CTTGGTGGAAAGAAG | 4067 |
rs71519442 | snp | G/T | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55927393 | AATATGCATTTAAGG[G/T]TCCTCTATGTCCTTT | 4067 |
rs71531255 | snp | A/G | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55908997 | TGTGTATGTGTATAT[A/G]TATATATATATATAT | 4067 |
rs71555624 | in-del | -/G | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55885975 | GCGGGGTGGGAGAGA[-/G]GGAGCAGTCTAGAGT | 4067 |
rs71555625 | in-del | -/A | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55943575 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 4067 |
rs71555626 | in-del | -/C | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55966666 | AGCCACCTCCCCCGG[-/C]TAGATTTTCTGTTTT | 4067 |
rs71555629 | in-del | -/G | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:56004558 | TCAGCCTCCCAAAGT[-/G]GCAGGGATTACAGGC | 4067 |
rs72534424 | snp | C/G | | | intron-variant | LYN | GRCh38.p7 | 8:55911682 | CAGTCCTATGAGCTG[C/G]GGGGCACCTGCCCTG | 4067 |
rs72651454 | snp | A/G | 0.159622 | 0.233092 | upstream-variant-2KB, utr-variant-5-prime | LYN | GRCh38.p7 | 8:55878887 | GTCAGCCTCTTCAGA[A/G]CATTGTTAATGAGAG | 4067 |
rs72651456 | snp | A/T | 0.159292 | 0.232964 | upstream-variant-2KB, utr-variant-5-prime | LYN | GRCh38.p7 | 8:55879354 | ATCAATGCCCTGAAC[A/T]GCCTCCTGTACACCC | 4067 |
rs72651457 | snp | C/T | 0.155987 | 0.23165 | intron-variant | LYN | GRCh38.p7 | 8:55885119 | TTGGCATGAGCTGAC[C/T]GTGTATGGGAAGAGA | 4067 |
rs72651459 | snp | C/G | 0.16911 | 0.236552 | intron-variant | LYN | GRCh38.p7 | 8:55897288 | AGTTTAGATTAAGAA[C/G]AGTAAAGCTTTCTCT | 4067 |
rs72651463 | snp | C/T | 0.24449 | 0.249939 | intron-variant | LYN | GRCh38.p7 | 8:55902374 | GCTCTGTAGCCCAGA[C/T]TGGAGTGCAGTGGCG | 4067 |
rs72651464 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LYN | GRCh38.p7 | 8:55902500 | GCCCAGCTAATTTTT[C/T]TTTTCTAGAAGTTGA | 4067 |
rs72651466 | snp | A/G | 0.1652 | 0.235179 | intron-variant | LYN | GRCh38.p7 | 8:55903356 | TTGAGGTGTTTATTT[A/G]AAGTATTCAAAAGAA | 4067 |
rs72651467 | snp | G/T | 0.15665 | 0.231917 | intron-variant | LYN | GRCh38.p7 | 8:55903522 | TCATGAGCTGAATAG[G/T]TTGAAAATTTGCTGC | 4067 |
rs72651469 | snp | A/T | 0.0988009 | 0.199095 | intron-variant | LYN | GRCh38.p7 | 8:55903939 | ATGGGAGGATCCGCT[A/T]GAGCCTCGGAGGTTG | 4067 |
rs72651470 | snp | A/G | 0.152667 | 0.230274 | intron-variant | LYN | GRCh38.p7 | 8:55903984 | TGTGATTGTGCCATT[A/G]CAACAGAGTAAGACA | 4067 |
rs72651474 | snp | C/T | 0.144632 | 0.226711 | intron-variant | LYN | GRCh38.p7 | 8:55909308 | ACCCCAGTCCTGGCA[C/T]TGGGGAGAGTAGTCC | 4067 |
rs72651476 | snp | A/T | 0.145305 | 0.227022 | intron-variant | LYN | GRCh38.p7 | 8:55916727 | TGTGGCAATGGCAGC[A/T]TTGCCCTTTACCCCA | 4067 |
rs72651478 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | LYN | GRCh38.p7 | 8:55918357 | CCCCTGTGGAGATGT[A/G]AAAACACTGATGCCC | 4067 |
rs72651479 | snp | C/T | 0.128288 | 0.218372 | intron-variant | LYN | GRCh38.p7 | 8:55926541 | AGCTCTTATCAGTTA[C/T]TTTCTGAACCTAAAA | 4067 |
rs72651480 | snp | G/T | 0.240478 | 0.249819 | intron-variant | LYN | GRCh38.p7 | 8:55926594 | CCAAGAAGATCTAAT[G/T]AAATTCTATTGTATT | 4067 |
rs72651481 | snp | A/C | 0.130351 | 0.219509 | intron-variant | LYN | GRCh38.p7 | 8:55926600 | AGATCTAATGAAATT[A/C]TATTGTATTTTAAAC | 4067 |
rs72651482 | snp | G/T | 0.142609 | 0.225759 | intron-variant | LYN | GRCh38.p7 | 8:55927968 | TGGTAAGGGTATTGT[G/T]TAGTTTTATAAGAAA | 4067 |
rs72651483 | snp | C/T | 0.142609 | 0.225759 | intron-variant | LYN | GRCh38.p7 | 8:55928540 | TCTTCTTTGGTGAGG[C/T]GTCTATTCAGATCTG | 4067 |
rs72651484 | snp | C/T | 0.142609 | 0.225759 | intron-variant | LYN | GRCh38.p7 | 8:55929033 | CAGTTGTTCCAGTAC[C/T]ACTTATTGAAAAAAA | 4067 |
rs72651485 | snp | G/T | 0.128288 | 0.218372 | intron-variant | LYN | GRCh38.p7 | 8:55930495 | GATATACATAATTCA[G/T]ACTCTGCTTTGAATG | 4067 |
rs72651488 | snp | C/T | 0.128288 | 0.218372 | intron-variant | LYN | GRCh38.p7 | 8:55933076 | CTTGCAACATACCCA[C/T]GTAACAAACCTGCAC | 4067 |
rs72651489 | snp | C/T | 0.143284 | 0.226079 | intron-variant | LYN | GRCh38.p7 | 8:55933081 | AACATACCCATGTAA[C/T]AAACCTGCACATGTA | 4067 |
rs72651490 | snp | A/C | 0.143284 | 0.226079 | intron-variant | LYN | GRCh38.p7 | 8:55933690 | GGCTTCCTGAGTTCA[A/C]CACTGTCTCATTATC | 4067 |
rs72651492 | snp | A/T | 0.142947 | 0.22592 | intron-variant | LYN | GRCh38.p7 | 8:55934332 | AATCTTTTCAAATGT[A/T]GTCTGTCTTCCATCA | 4067 |
rs72651493 | snp | A/T | 0.0850919 | 0.187897 | intron-variant | LYN | GRCh38.p7 | 8:55942964 | ATCCTGAAGTTGTCA[A/T]CTGTTATTTTAGTGA | 4067 |
rs72651494 | snp | A/G | 0.275464 | 0.2487 | intron-variant | LYN | GRCh38.p7 | 8:55945663 | ATGTGGCACTGTGAA[A/G]AAAAGAATTTGATTT | 4067 |
rs72651497 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | LYN | GRCh38.p7 | 8:55956649 | TTCCCTCTTAGAAGC[C/T]GTCACTTCTCTATAA | 4067 |
rs72651500 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | LYN | GRCh38.p7 | 8:55959078 | ACATTCCCATTGACC[A/G]TGTGTAAGTGTTCCC | 4067 |
rs72651502 | snp | A/G | 0.155656 | 0.231515 | intron-variant | LYN | GRCh38.p7 | 8:55962974 | CTCTTGTGAACTAAT[A/G]GAGCGAGAACTCACT | 4067 |
rs72653908 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYN | GRCh38.p7 | 8:55969846 | GCAAAGACTTCCCTG[C/T]GTCAAATTCATGAAG | 4067 |
rs72653917 | snp | A/T | 0.15698 | 0.23205 | intron-variant | LYN | GRCh38.p7 | 8:55980285 | TGGAGTGCAGTGGCT[A/T]TTCACAGGCATGATG | 4067 |
rs72653918 | snp | G/T | | | intron-variant | LYN | GRCh38.p7 | 8:55981648 | GGTGTGAGCCACCGT[G/T]CCCGGCCAGAACACA | 4067 |
rs72653921 | snp | C/T | 0.156319 | 0.231784 | intron-variant | LYN | GRCh38.p7 | 8:55984598 | AAGTCCTGCACATGG[C/T]CACTCTGACCCAACT | 4067 |
rs72653924 | snp | C/T | 0.157311 | 0.232183 | intron-variant | LYN | GRCh38.p7 | 8:55993529 | CTTTGAGGTCAGACA[C/T]GCCTGGTGTAAATGG | 4067 |
rs72653928 | snp | A/G | 0.157311 | 0.232183 | intron-variant | LYN | GRCh38.p7 | 8:55995176 | CCTGACGCCCTCACC[A/G]TGCCACTGCCTGCTG | 4067 |
rs73590303 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | LYN | GRCh38.p7 | 8:55949651 | ACGGATCAAGTCAGC[A/G]TAATTAGCATATCCA | 4067 |
rs73590305 | snp | A/G | 0.159951 | 0.233219 | intron-variant | LYN | GRCh38.p7 | 8:55951092 | TACAAGAAATACAAA[A/G]CTTAGCCAGGCCTGG | 4067 |
rs73590319 | snp | A/G | 0.141934 | 0.225437 | intron-variant | LYN | GRCh38.p7 | 8:55957793 | ATCAAAAATACAAAA[A/G]AAAATTAGTTGAGCA | 4067 |
rs73590328 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | LYN | GRCh38.p7 | 8:55963848 | ATTTTCATCTATTTT[A/G]TATCATGTATTTTCC | 4067 |
rs73590337 | snp | A/C/G | 0.0217236 | 0.101931 | intron-variant | LYN | GRCh38.p7 | 8:55971245 | CTGTCCTCAAAGTCT[A/C/G]TGCTGGCCCCTGGGA | 4067 |
rs73590350 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | LYN | GRCh38.p7 | 8:55982343 | TTTTTGAATATTTGC[A/G]TTATACTTACTGATT | 4067 |
rs73590352 | snp | A/C/G | 0.0781991 | 0.181807 | intron-variant | LYN | GRCh38.p7 | 8:55983374 | TGTTCTAGAAATTCC[A/C/G]CATTAGCGTTTTCCC | 4067 |
rs73590356 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | LYN | GRCh38.p7 | 8:55989726 | AGAGGTTTATTTTGC[C/T]GAGGTTGAGGACCAT | 4067 |
rs73590364 | snp | G/T | 0.0640965 | 0.167152 | intron-variant | LYN | GRCh38.p7 | 8:55997776 | GTCTTGAAAAGATTC[G/T]TCACACATTAGAAAA | 4067 |
rs73590367 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | LYN | GRCh38.p7 | 8:55998112 | AAAATGTTAAGACAT[C/G]TTCCTTTTTTTTTTT | 4067 |
rs73590370 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | LYN | GRCh38.p7 | 8:55999124 | ATTCTTATGCTCTCA[C/T]CCACGAGAGCTGAGC | 4067 |
rs73590371 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | LYN | GRCh38.p7 | 8:56000399 | AGATTCTGACCATCC[C/T]TCCATTTTTCCATGG | 4067 |
rs73590372 | snp | A/G | 0.34989 | 0.229177 | intron-variant | LYN | GRCh38.p7 | 8:56003773 | GAAAGTCACATATAA[A/G]GCAAACTCATTTTTA | 4067 |
rs73590374 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | LYN | GRCh38.p7 | 8:56006003 | GGTGGGAGGATCACC[A/G]AGCCCAGGGAGTTTG | 4067 |
rs73604828 | snp | A/G | 0.0325976 | 0.123435 | upstream-variant-2KB | LYN | GRCh38.p7 | 8:55876832 | AAGCACCATGACCAC[A/G]CATGAGATGATGATG | 4067 |
rs73604837 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | LYN | GRCh38.p7 | 8:55883298 | AGGTCATTTAACAAA[C/T]ATTTTAAAAGTGAAA | 4067 |
rs73604846 | snp | A/C | 0.0678174 | 0.1712 | intron-variant | LYN | GRCh38.p7 | 8:55889015 | CACGTGTATTTCTTT[A/C]TTTATTTATTTGTAT | 4067 |
rs73604848 | snp | A/C/G | 0.127944 | 0.218179 | intron-variant | LYN | GRCh38.p7 | 8:55889178 | CGCCACCAGGCCTGC[A/C/G]TAATTTTTTTGTTTT | 4067 |
rs73604850 | snp | A/G | 0.132409 | 0.220618 | intron-variant | LYN | GRCh38.p7 | 8:55889228 | GGATAATTTGAGCTC[A/G]GGAGTTTGAGACCAG | 4067 |
rs73604862 | snp | A/C | 0.0962929 | 0.197165 | intron-variant | LYN | GRCh38.p7 | 8:55895602 | CAAGACCAGGCTGGG[A/C]ATCATAGTGAGACCT | 4067 |
rs73604869 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | LYN | GRCh38.p7 | 8:55897195 | AATTTCTCCTGATAA[A/G]GAGCTGAAAATCAAG | 4067 |
rs73604874 | snp | A/G | 0.0425829 | 0.139564 | intron-variant | LYN | GRCh38.p7 | 8:55897402 | AGGGAGCATTCTGAC[A/G]CTGAGCACACCTCTG | 4067 |
rs73606807 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | LYN | GRCh38.p7 | 8:55905834 | GGGACTTCCCATTAG[G/T]CCTGGAGTGTCTCCC | 4067 |
rs73606851 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | LYN | GRCh38.p7 | 8:55918781 | GGCAAACCCCACCAC[C/T]GGGCCAGCCAACTAC | 4067 |
rs73606853 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | LYN | GRCh38.p7 | 8:55921943 | CAAGGGTGTGCAAAA[C/G]TGACAGGAATCCCTG | 4067 |
rs73606857 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LYN | GRCh38.p7 | 8:55924308 | TCATGGTACAGGCCT[A/G]TTCTATACCATCTGT | 4067 |
rs73606861 | snp | C/G | 0.0471551 | 0.14613 | intron-variant | LYN | GRCh38.p7 | 8:55924510 | TGGGATTACAGGCGT[C/G]CACCCACCATGCCCG | 4067 |
rs73606869 | snp | C/T | 0.0663309 | 0.169604 | intron-variant | LYN | GRCh38.p7 | 8:55925689 | GGCATCAGAATGGAA[C/T]GGAAACACCATCTAG | 4067 |
rs73606871 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | LYN | GRCh38.p7 | 8:55925956 | TTAATATTGCTTCCA[A/G]ACATTTTTATTATGT | 4067 |
rs73606873 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | LYN | GRCh38.p7 | 8:55929896 | CAACCCCTGGGCCAT[A/G]GACTGGTACTGGTCT | 4067 |
rs73606874 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | LYN | GRCh38.p7 | 8:55933414 | CCAAACAGTCCCACA[A/G]TAAGTATTCTCTTGT | 4067 |
rs73606879 | snp | A/G | 0.0486741 | 0.148216 | intron-variant | LYN | GRCh38.p7 | 8:55938835 | ATGACTTAGACTTGA[A/G]AGCGCACTCCTGTGT | 4067 |
rs73606886 | snp | A/T | 0.0275645 | 0.114116 | intron-variant | LYN | GRCh38.p7 | 8:55944357 | TAAAATAAGAGAAAT[A/T]AGAGTCACAAATAGT | 4067 |
rs73606887 | snp | A/T | 0.0275645 | 0.114116 | intron-variant | LYN | GRCh38.p7 | 8:55944400 | ATCAGAGTTCTCAAA[A/T]AAAGATCTGATTTTT | 4067 |
rs73679604 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | LYN | GRCh38.p7 | 8:55970444 | ACTTGAATGATGCCA[A/G]CTGCTGGCTTTTACT | 4067 |
rs73679618 | snp | G/T | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55991392 | CTGTTCAGCTGACTG[G/T]CAGTGGAGGAAGAGG | 4067 |
rs73679619 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | LYN | GRCh38.p7 | 8:55994852 | AGCTATGACCGCTCA[A/G]TTGCTGCTGTCTCAT | 4067 |
rs73679620 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | LYN | GRCh38.p7 | 8:55998760 | ATGCAAAACACAAAT[A/G]GATTCAGCAAGATGA | 4067 |
rs73679621 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | LYN | GRCh38.p7 | 8:56001243 | TTTGATGGATGGATG[A/G]GTGAATGAATGAATG | 4067 |
rs73682014 | snp | A/G | 0.0799831 | 0.183287 | intron-variant, upstream-variant-2KB | LYN | GRCh38.p7 | 8:55923503 | AACCCGACAGCAGAA[A/G]AAATACAGGAGAGTT | 4067 |
rs73682015 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | LYN | GRCh38.p7 | 8:55924065 | TTTTTCTTTTTCTTT[C/T]TTTTTTTTTTTTATT | 4067 |
rs73682016 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | LYN | GRCh38.p7 | 8:55924204 | GTGTGAGAGATGTCA[C/T]TGTGTTTCCCTTGAA | 4067 |
rs73682019 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | LYN | GRCh38.p7 | 8:55926537 | TCCCAGCTCTTATCA[A/G]TTATTTTCTGAACCT | 4067 |
rs73682020 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | LYN | GRCh38.p7 | 8:55935260 | CTTAAGTAGGGCCTT[A/G]TGTTGCAGGCTGGTC | 4067 |
rs73682022 | snp | A/G | 0.0163024 | 0.0888001 | intron-variant | LYN | GRCh38.p7 | 8:55951929 | GCAGATCTTATTTGT[A/G]AGATATAAACATTTA | 4067 |
rs73682107 | snp | A/G | 0.0729998 | 0.176553 | intron-variant | LYN | GRCh38.p7 | 8:55905857 | TGTCTCCCATGCAAA[A/G]AGCCCGCTCCTCTGT | 4067 |
rs73682123 | snp | G/T | 0.0655868 | 0.168795 | intron-variant | LYN | GRCh38.p7 | 8:55917742 | ATTCAAAGATTTATA[G/T]AATTAGAGTTAAAAG | 4067 |
rs73682124 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | LYN | GRCh38.p7 | 8:55917805 | AAGGAATATGCTTGA[A/G]ATATTCAATGGCAGA | 4067 |
rs73682126 | snp | C/G | 0.031825 | 0.122064 | intron-variant | LYN | GRCh38.p7 | 8:55919577 | GTCTTAACTATTAGG[C/G]AAATTTAGCTTCCTG | 4067 |
rs73682127 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | LYN | GRCh38.p7 | 8:55919988 | ACTTAACATGGCTTG[A/G]GGCTGAAAAACAGAA | 4067 |
rs73684163 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | LYN | GRCh38.p7 | 8:55883595 | ACCTGAGTAATACTT[C/T]GCAAAAGGACTTTCC | 4067 |
rs73684164 | snp | C/T | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55884856 | AGCCTTTGTTGTTTA[C/T]CCCCTTCATCCTGTT | 4067 |
rs74202955 | in-del | -/AC/CATACATATATATATATATATACATACACGTATATATACGTATATATATACACATACATATATATACGTGTATATATATGTACATATATATA | 0.386884 | 0.209196 | intron-variant | LYN | GRCh38.p7 | 8:55911077 | ATTTATATATATATA[lengthTooLong]TACGTATATAGATAT | 4067 |
rs74380219 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | LYN | GRCh38.p7 | 8:55891676 | TTATATACTTAAAAT[A/C]GTTACGATACAAGTT | 4067 |
rs74384455 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | LYN | GRCh38.p7 | 8:56006376 | GAGACTGTACTCCCA[A/G]GGTATCTAGCTCTTC | 4067 |
rs74385326 | snp | A/G | 0.0955749 | 0.196603 | intron-variant | LYN | GRCh38.p7 | 8:55901844 | CTCAACCAAAGATAA[A/G]CAGGGAAGAACCTAA | 4067 |
rs74392075 | snp | C/G/T | 0.00358923 | 0.042236 | intron-variant | LYN | GRCh38.p7 | 8:55939537 | AGGAACGCAGTGGGG[C/G/T]GGGGACAGGGGATTC | 4067 |
rs74409019 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | LYN | GRCh38.p7 | 8:55983539 | CAGTTCTTCCCCACC[C/T]GCCCTCTCTTGAACC | 4067 |
rs74437529 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | LYN | GRCh38.p7 | 8:55973815 | GCCAAACAAAGTGGC[A/G]TGCACCTATTGTCTC | 4067 |
rs74448907 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | LYN | GRCh38.p7 | 8:55967263 | CCCAGAATTCTAATA[C/T]TACAGATTTAGTACG | 4067 |
rs74464209 | snp | C/G | 0.160938 | 0.233598 | intron-variant | LYN | GRCh38.p7 | 8:55880435 | TTCCCGGTGAGGGCC[C/G]GAGGGCCGGCTGCTG | 4067 |
rs74607441 | snp | A/C | 0.0205511 | 0.0992634 | intron-variant | LYN | GRCh38.p7 | 8:56006075 | GGCAACAGAGTGAGA[A/C]CCTGTCTCAAAAAAA | 4067 |
rs74615681 | snp | A/T | 0.030278 | 0.119257 | intron-variant | LYN | GRCh38.p7 | 8:55956589 | GTTTAAGATTATGTA[A/T]ATAGAACTTTCTCCA | 4067 |
rs74624721 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | LYN | GRCh38.p7 | 8:55949159 | TTCTTCTTTTCATAG[G/T]GTCCATCTCTATGAT | 4067 |
rs74625967 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | LYN | GRCh38.p7 | 8:55965391 | GTGGAGGGAGTGGCT[C/T]CCTGTCCTTTTAGTG | 4067 |
rs74634884 | snp | A/C | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55977508 | TCAGCTTTTCATGCT[A/C]CTAACATTTTGTTTT | 4067 |
rs74652297 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | LYN | GRCh38.p7 | 8:55975324 | AGAAATCACTGAGCC[A/C]AGAACCAGAAAACCT | 4067 |
rs74655847 | snp | A/C | 0.0704125 | 0.17392 | intron-variant | LYN | GRCh38.p7 | 8:55896676 | ATTTTAAAAAAAAGA[A/C]ACATAGAATAAAAAC | 4067 |
rs74692140 | snp | C/G | 0.0383715 | 0.133092 | intron-variant | LYN | GRCh38.p7 | 8:56007307 | TCTTCTGAAATTTAT[C/G]CAAGTTATAAGAGCC | 4067 |
rs74809667 | snp | C/T | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55987177 | CAGCACTTTGGGAGG[C/T]TAAGGCAGGCGGATC | 4067 |
rs74868519 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | LYN | GRCh38.p7 | 8:55962070 | CTTTTACGTCTTGCC[C/T]CTTTTACTCAACGGG | 4067 |
rs74868909 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | LYN | GRCh38.p7 | 8:56003416 | CCAGGTGTGGTGGCT[C/T]ATGCCTGTAATCCCA | 4067 |
rs74944310 | snp | C/T | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55887577 | ATATATATATATATA[C/T]ACACACACACACACA | 4067 |
rs75153775 | snp | A/G | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55929042 | CAGTACCACTTATTG[A/G]AAAAAATATCCTTTC | 4067 |
rs75156240 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | LYN | GRCh38.p7 | 8:56008752 | CTTACTTCTCTCCTG[A/G]AGGTCAGGAATATGC | 4067 |
rs75160967 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | LYN | GRCh38.p7 | 8:55914489 | CTCAGAGAGGCACTA[G/T]GCAGTGAATCAAGCC | 4067 |
rs75255237 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | LYN | GRCh38.p7 | 8:55982620 | TCCTCGGATCCCCGA[A/G]CACTCCTCCTTGCTG | 4067 |
rs75288345 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | LYN | GRCh38.p7 | 8:55924076 | CTTTCTTTTTTTTTT[-/TT]ATTATAGCAACCACA | 4067 |
rs75291057 | snp | C/G | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55966028 | TACTCAGGAGGCTCA[C/G]GCATAAGAATCGCTT | 4067 |
rs75299198 | snp | C/G | 0.0744748 | 0.178019 | intron-variant | LYN | GRCh38.p7 | 8:55971105 | TGGCAAGCCTAACAG[C/G]TTCCTCATCTGAGTT | 4067 |
rs75314857 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | LYN | GRCh38.p7 | 8:55885432 | GCTCACTCCTCTTTA[C/T]TGACACCAGACCATA | 4067 |
rs75338233 | snp | G/T | 0.123452 | 0.215605 | intron-variant | LYN | GRCh38.p7 | 8:55956960 | CATTGACATTCTCAC[G/T]TACTCATTGCTGTAG | 4067 |
rs75404716 | snp | C/T | 0.132066 | 0.220435 | intron-variant | LYN | GRCh38.p7 | 8:55882412 | AGATTCCAGTTGGTT[C/T]ACATGACTATGTGGA | 4067 |
rs75413466 | snp | A/G | 0.0696718 | 0.173152 | intron-variant | LYN | GRCh38.p7 | 8:55939937 | ATTTTGGGAACTGCA[A/G]CTCGCTAGTTTCAGA | 4067 |
rs75437998 | snp | A/T | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55900389 | ATTTTTAATTTTTTT[A/T]AGGGATAGGATTTCA | 4067 |
rs75446409 | snp | G/T | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55894552 | TTTTTTTTTTTTTTT[G/T]GACGGAGTCTTGTTC | 4067 |
rs75467789 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYN | GRCh38.p7 | 8:55892683 | AAAGTCCTGGGATTA[C/T]GAGCATGAGCCATTG | 4067 |
rs75501935 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | LYN | GRCh38.p7 | 8:55907360 | AATAAAATAAGTCAA[A/G]CAGATAAGAATATGC | 4067 |
rs75549139 | snp | G/T | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:56004309 | CTTTTTTTTTTTTTT[G/T]TTGAGACAGAGTCTC | 4067 |
rs75568524 | in-del | -/AAA | | | intron-variant | LYN | GRCh38.p7 | 8:55951676 | TTTCAAAAAAAAAAA[-/AAA]GAAAATCAAAGTAAC | 4067 |
rs75569658 | snp | C/G | 0.0726307 | 0.176182 | intron-variant | LYN | GRCh38.p7 | 8:55906100 | AAGTCAGAGGGCTGG[C/G]ATGGTGAGGTCGCCC | 4067 |
rs75573514 | snp | A/G | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55891736 | AAAGAATGAAAAAAA[A/G]GTTGCTTGATGAGCA | 4067 |
rs75573662 | snp | A/G | 0.164873 | 0.23506 | intron-variant | LYN | GRCh38.p7 | 8:55890444 | ATAATAAGTGGTGCC[A/G]AGGATGTGGAGAAAT | 4067 |
rs75664300 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | LYN | GRCh38.p7 | 8:55946275 | CCCTGTCACTGGCCA[A/G]GCAGGGCAGGATGCA | 4067 |
rs75804002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYN | GRCh38.p7 | 8:55988039 | GATAACCAAATAAAG[C/T]TAAAATAAAATTTCC | 4067 |
rs75844501 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LYN | GRCh38.p7 | 8:55937528 | TATAAGTCATGCTAG[C/T]GGGAACATCCTTATG | 4067 |
rs75854962 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | LYN | GRCh38.p7 | 8:55904435 | TCAATCACAGACCAC[C/G]CTTTTTTCTGAGCAT | 4067 |
rs75868327 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | LYN | GRCh38.p7 | 8:56006904 | TTGTCATTTAATAGC[A/G]GATTTTATTTATTGC | 4067 |
rs75918249 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | LYN | GRCh38.p7 | 8:56007398 | TACAAATCTGTCTTT[C/T]GCTTTAAGCAATGAA | 4067 |
rs75926223 | snp | G/T | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55902865 | GAGGCTTTTTTTTTT[G/T]GGAGACGGAGTCTCT | 4067 |
rs75955525 | snp | A/G | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55978978 | CATGCTTCCCTGACC[A/G]CTCAGCATGCCTCAC | 4067 |
rs75962225 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | LYN | GRCh38.p7 | 8:55963017 | GATGGCCCCAAGCCA[C/T]TCATGAGGGATTCAT | 4067 |
rs76032475 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | LYN | GRCh38.p7 | 8:55991641 | AGTAGTTCTGTGCCT[C/T]CTCCCAGGACAGCAG | 4067 |
rs76039498 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYN | GRCh38.p7 | 8:55982550 | CACCCAGGACCCCCA[C/G]CTTTGGAGTCCACGC | 4067 |
rs76089859 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | LYN | GRCh38.p7 | 8:55949155 | GGTTTTCTTCTTTTC[A/G]TAGTGTCCATCTCTA | 4067 |
rs76126067 | snp | A/C | 0.0107304 | 0.0725162 | intron-variant | LYN | GRCh38.p7 | 8:55974918 | GATTGACATGGTTTG[A/C]GGTTTAACCAGGAGG | 4067 |
rs76155216 | snp | A/G | 0.0471551 | 0.14613 | utr-variant-3-prime | LYN | GRCh38.p7 | 8:56011574 | AACACCTGAACATCC[A/G]TTTATGGGGGCCAGA | 4067 |
rs76227211 | snp | A/T | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55959828 | CAATAAAAAAAAAAA[A/T]TGACCTGGCATACTT | 4067 |
rs76267427 | snp | A/C | 0.109461 | 0.206758 | intron-variant | LYN | GRCh38.p7 | 8:56007581 | ACAAGGGCTCTTCCA[A/C]GACAGAAATGATCAT | 4067 |
rs76286536 | snp | A/T | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55998129 | TCCTTTTTTTTTTTT[A/T]AAGATGACCATTGTT | 4067 |
rs76358467 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | LYN | GRCh38.p7 | 8:55970960 | GTCACATGCTTGGCA[C/T]GGACACAAGCACCTC | 4067 |
rs76400205 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | LYN | GRCh38.p7 | 8:55933800 | TTTAATTGTCTTGCA[A/G]TTCTTTTCTGGAAAC | 4067 |
rs76404221 | snp | A/T | 0.079617 | 0.182947 | intron-variant | LYN | GRCh38.p7 | 8:55924529 | CCACCATGCCCGGCT[A/T]ATTTTTGTATTTTTA | 4067 |
rs76429184 | snp | A/G | 0.095934 | 0.196885 | intron-variant | LYN | GRCh38.p7 | 8:55899523 | ATAAATATAATGCAG[A/G]GAACATTTATTGAGT | 4067 |
rs76469276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYN | GRCh38.p7 | 8:55985357 | AAAATGCAGGAGCAG[C/T]CACAGAGAGCAGACG | 4067 |
rs76483933 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | LYN | GRCh38.p7 | 8:55923899 | ATTTGAAAAAAAAAA[A/T]TACACATACATTGAA | 4067 |
rs76635715 | snp | A/T | | | intron-variant | LYN | GRCh38.p7 | 8:55928402 | CCGCCGACCTTGGCC[A/T]CCCAAAGTGCTGGGA | 4067 |
rs76668941 | snp | G/T | | | intron-variant | LYN | GRCh38.p7 | 8:55909977 | AATGGGGTTGTTTGT[G/T]TGTGTGTGTGTGTGT | 4067 |
rs76732917 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | LYN | GRCh38.p7 | 8:55914693 | CCTTTTCATCAGCCT[C/T]GCTCACCTTACCCTT | 4067 |
rs76842358 | snp | A/C | | | intron-variant | LYN | GRCh38.p7 | 8:55898862 | ATAGACAGTTTCTTG[A/C]TCTGATGCCTGGAGT | 4067 |
rs76845238 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYN | GRCh38.p7 | 8:55973101 | GGGCAGAGTTGGGAC[G/T]TTTCCCACCATCTGT | 4067 |
rs76874815 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | LYN | GRCh38.p7 | 8:55913751 | TCTGGGGATTCGGCA[C/G]AGTTTTTATGGAGGA | 4067 |
rs76883082 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | LYN | GRCh38.p7 | 8:55929262 | GAATAGATCCTTCTT[A/C]CTGTTTCTTCCATCT | 4067 |
rs76884513 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | LYN | GRCh38.p7 | 8:56001797 | ATCTCATAAAAGAAT[A/G]TTTTGTGATATGCGT | 4067 |
rs76899232 | snp | A/T | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55946946 | ATAGTGAATAATATT[A/T]CCTTGTAAGTATATG | 4067 |
rs76911350 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | LYN | GRCh38.p7 | 8:55932121 | GAAATAAGGAAAGGA[A/G]GTGTTCCTGTGCATA | 4067 |
rs76946724 | snp | C/T | 0.149999 | 0.229128 | intron-variant | LYN | GRCh38.p7 | 8:55909458 | CACAGATGGCAGATT[C/T]GCCCCATTGGCTCCT | 4067 |
rs76950468 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | LYN | GRCh38.p7 | 8:55961148 | AATCAACTGCATGCA[C/T]TTTTTAAAAACCACT | 4067 |
rs76988198 | snp | C/T | 0.030278 | 0.119257 | intron-variant | LYN | GRCh38.p7 | 8:55887938 | TAAAACGGCAGGATA[C/T]AAGGAGCAATGGAAT | 4067 |
rs77011725 | snp | G/T | 0.0596104 | 0.162024 | intron-variant | LYN | GRCh38.p7 | 8:56008452 | TTTGCATGACATACA[G/T]TCTTCTCTAGAGAAG | 4067 |
rs77017062 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | LYN | GRCh38.p7 | 8:55897486 | GTAACAGTTCTGTCT[C/T]ACTGTTCAAATTTGC | 4067 |
rs77035567 | snp | C/T | 0.0799831 | 0.183287 | intron-variant | LYN | GRCh38.p7 | 8:55937329 | GTAATTGGCAAAAAC[C/T]GCAATTACTTTTGCA | 4067 |
rs77060457 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | LYN | GRCh38.p7 | 8:55908642 | GTGCAGTTTTGTTAC[A/G]CGGATATATTGCAGA | 4067 |
rs77081031 | snp | A/G | 0.078151 | 0.181571 | intron-variant | LYN | GRCh38.p7 | 8:55925053 | CACCATGTTGGCCAA[A/G]CTGGGGTGATCCGCT | 4067 |
rs77111748 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | LYN | GRCh38.p7 | 8:55977875 | AGTGAGCTATGATTA[C/T]ACCCACCGCCCTCCA | 4067 |
rs77115555 | snp | G/T | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55907569 | GGTGCTTTTTTTTTG[G/T]TGGAAAATCAAACTT | 4067 |
rs77130049 | snp | C/G | | | intron-variant | LYN | GRCh38.p7 | 8:55902471 | TAGCTGGAATTACAG[C/G]TGCGCTCCACAACGC | 4067 |
rs77172803 | snp | A/T | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55987422 | AAAAAAAAAAAAAAA[A/T]ATCTTTTCTGTTTAT | 4067 |
rs77179240 | snp | A/G | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55900390 | TTTTTAATTTTTTTT[A/G]GGGATAGGATTTCAT | 4067 |
rs77361422 | snp | A/G | 0.111224 | 0.207945 | intron-variant | LYN | GRCh38.p7 | 8:55927877 | CTGCTATAAACATCT[A/G]TGTGCAGGTTTTTGT | 4067 |
rs77365008 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | LYN | GRCh38.p7 | 8:55902713 | ACATATTTTACTCAT[A/G]AGCATGGCAAAATGT | 4067 |
rs77375140 | snp | G/T | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55891737 | AAGAATGAAAAAAAA[G/T]TTGCTTGATGAGCAG | 4067 |
rs77412240 | snp | C/G | 0.0325976 | 0.123435 | intron-variant | LYN | GRCh38.p7 | 8:55991049 | ACAAATAGAGACACG[C/G]CGGCAGTACTACCAC | 4067 |
rs77523501 | snp | A/G | 0.149889 | 0.229752 | intron-variant | LYN | GRCh38.p7 | 8:55949958 | GCCCTAGGAAACCAC[A/G]AATCTACTTTTTATC | 4067 |
rs77616302 | snp | C/G | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55953248 | CACATTTTATTAAGT[C/G]TGACAATCTGGCAGC | 4067 |
rs77652119 | snp | A/C | | | intron-variant | LYN | GRCh38.p7 | 8:55909455 | TCCCACAGATGGCAG[A/C]TTCGCCCCATTGGCT | 4067 |
rs77738083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYN | GRCh38.p7 | 8:55925638 | GTTATTATTACCTTT[C/T]TCATGGGTGAGGAAG | 4067 |
rs77845011 | snp | C/G | 0.109461 | 0.206758 | intron-variant | LYN | GRCh38.p7 | 8:55903636 | TTGATAATCTAATCT[C/G]AATAATTAAGTTTTA | 4067 |
rs77846507 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LYN | GRCh38.p7 | 8:55996497 | TCAGAGTTTTCTCTA[A/C]CTGCTTACCAGATAA | 4067 |
rs77849362 | snp | C/T | 0.0693013 | 0.172766 | intron-variant | LYN | GRCh38.p7 | 8:55958504 | AAATTTGTGTTTTAG[C/T]GATGTTTAGGTGTAC | 4067 |
rs77891046 | snp | A/G | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55998087 | AGACTCCGTCTCAAG[A/G]AAAAAAAAGAAAATG | 4067 |
rs77931075 | snp | A/G/T | 8.5665e-05 | 0.00654419 | intron-variant | LYN | GRCh38.p7 | 8:55950824 | TTAAAACACTATTTA[A/G/T]GAAATTATTTTTAGA | 4067 |
rs77932004 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | LYN | GRCh38.p7 | 8:55911979 | AGTGAGCTCAATATC[A/G]TCGTGGTGTGTTCTA | 4067 |
rs77935663 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LYN | GRCh38.p7 | 8:55953110 | ATTCCTGTGTGCATC[C/T]GGCACATGCTGAGGG | 4067 |
rs77962381 | snp | A/G | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55966019 | AAACCCAGCTACTCA[A/G]GAGGCTCAGGCATAA | 4067 |
rs77982534 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | LYN | GRCh38.p7 | 8:55973364 | GATCAAGAAATCCTG[A/G]CTACAGCAGCTTTAC | 4067 |
rs77991032 | snp | A/T | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55919023 | AGACCCTGTCTCTAC[A/T]AAAAAAAAAAAAAAA | 4067 |
rs77991616 | snp | C/G | 0.0228947 | 0.104514 | downstream-variant-500B | LYN | GRCh38.p7 | 8:56012775 | TATAATGTATGCTCA[C/G]TCTTGAGAGTCACCA | 4067 |
rs78033935 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | LYN | GRCh38.p7 | 8:55965534 | TATAAAGAACACCTT[C/T]TTTAAAGAAAATGTG | 4067 |
rs78041439 | snp | A/C | | | intron-variant | LYN | GRCh38.p7 | 8:55917778 | GATATCTTGTTTGAC[A/C]CTGAAAAAATTAAGG | 4067 |
rs78063917 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | LYN | GRCh38.p7 | 8:55924259 | CTGTGACTTCACCAT[A/G]GCACCGGGAGGGCCT | 4067 |
rs78066822 | snp | A/T | | | intron-variant | LYN | GRCh38.p7 | 8:55966368 | CAAAGTGAAGTTTTA[A/T]TTTTTTTTTTTTTAA | 4067 |
rs78095318 | snp | G/T | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55894553 | TTTTTTTTTTTTTTT[G/T]ACGGAGTCTTGTTCT | 4067 |
rs78151910 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | LYN | GRCh38.p7 | 8:56007742 | GTACATAAAGCAAAC[A/G]TTTCATAAAACCATA | 4067 |
rs78165300 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | LYN | GRCh38.p7 | 8:55976785 | CAGGGATGGGTCTTC[A/T]GTTGTAGGAACCTCG | 4067 |
rs78187646 | snp | C/G | 0.0236746 | 0.106192 | intron-variant | LYN | GRCh38.p7 | 8:55881499 | TCCAGTTAGTCCCTC[C/G]ATTCTCATTTGGAGG | 4067 |
rs78366878 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | LYN | GRCh38.p7 | 8:55986766 | ATCTCTTTCTGTTGT[C/T]CTAGGCTAGAGAGCA | 4067 |
rs78396160 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | LYN | GRCh38.p7 | 8:55915816 | GAAAGAGAGAGAGAA[A/G]AGAGAAAGAGAGCGA | 4067 |
rs78411918 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | LYN | GRCh38.p7 | 8:55969521 | ACATGCCATGTTTCA[C/G/T]ATCAGGTCAAAGGTA | 4067 |
rs78412597 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | LYN | GRCh38.p7 | 8:55949790 | TCACAATACCATACA[A/G]TCCATCTACTTAAAG | 4067 |
rs78417506 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | LYN | GRCh38.p7 | 8:55972522 | AGTTTCTGCTCACTG[C/T]GCCTGCTCCCTCGTC | 4067 |
rs78457120 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | LYN | GRCh38.p7 | 8:55982070 | TCAGCACCTGTTGGC[A/C]GAGGTTGATGCTAGA | 4067 |
rs78510946 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | LYN | GRCh38.p7 | 8:55923889 | ACTTAGTGCCATTTG[A/G]AAAAAAAAAATACAC | 4067 |
rs78598186 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | LYN | GRCh38.p7 | 8:55983339 | ATCAGGTCTTGTGCT[C/T]TCTTGCTGTTTCAAG | 4067 |
rs78661830 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | LYN | GRCh38.p7 | 8:55960542 | AATATTGGGAATACA[A/G]CCAAAAGAGTTGTGA | 4067 |
rs78665434 | snp | C/T | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55887579 | ATATATATATATACA[C/T]ACACACACACACACA | 4067 |
rs78678428 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | LYN | GRCh38.p7 | 8:55944858 | TGTGCAAACCCACAC[A/G]CCGCTTTTTCCTCTT | 4067 |
rs78696954 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | LYN | GRCh38.p7 | 8:55913620 | TCAGCAAAGTGTAAA[C/T]GCCCGTAATGGGCTT | 4067 |
rs78829165 | snp | A/G | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:56000753 | AAAAAAAAAAAAAAA[A/G]AAGAGGGATTTCTCC | 4067 |
rs78850242 | snp | A/G | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55966035 | GAGGCTCAGGCATAA[A/G]AATCGCTTGAAACCA | 4067 |
rs78888833 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | LYN | GRCh38.p7 | 8:55887106 | TGTAAATATCTTAAA[A/G]GATAAAACATTCAAT | 4067 |
rs78891183 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | LYN | GRCh38.p7 | 8:55990837 | GGCCAAGGGGAGGGT[C/T]TACCCAGTTGGTTAA | 4067 |
rs78965273 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | LYN | GRCh38.p7 | 8:55971956 | TTCCAGGGGGCTTCA[C/G]TTGACTCTCCTGTCA | 4067 |
rs78972555 | snp | C/T | 0.131723 | 0.220251 | intron-variant | LYN | GRCh38.p7 | 8:55881404 | ACCTAAAGCCATGCC[C/T]TGGGGAATAGGCACT | 4067 |
rs78998014 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | LYN | GRCh38.p7 | 8:55984408 | CAGTGCCTATTACCC[C/T]CTTTTCCAAAACCTG | 4067 |
rs79117436 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | LYN | GRCh38.p7 | 8:55972087 | GCCAGGTGAACTCAT[A/G]TTCACAGGTCCAGGG | 4067 |
rs79149277 | snp | A/G | 0.145978 | 0.227331 | intron-variant | LYN | GRCh38.p7 | 8:55949427 | TTTAATTCCATCACG[A/G]AGAGTGAATTTTCCC | 4067 |
rs79153336 | snp | A/C | 0.0115144 | 0.0749975 | upstream-variant-2KB | LYN | GRCh38.p7 | 8:55876476 | CAAACTTGGCTGCTC[A/C]TTGGAACCACCTGGC | 4067 |
rs79163926 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | LYN | GRCh38.p7 | 8:55984823 | ATTTGCCTGCAGTGT[A/G]TGTCAGTCATGATGT | 4067 |
rs79264935 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | LYN | GRCh38.p7 | 8:55939346 | AATTATCCATGACAA[C/T]GGTGGAAAGAAATTA | 4067 |
rs79265928 | in-del | -/AT | | | intron-variant | LYN | GRCh38.p7 | 8:55957191 | ACAAACTCCAATCTT[-/AT]CAGTTGTTCAAAGGA | 4067 |
rs79297159 | snp | A/G | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:56000756 | AAAAAAAAAAAAAAA[A/G]AGGGATTTCTCCCAG | 4067 |
rs79307691 | snp | A/G | 0.0984431 | 0.198823 | intron-variant | LYN | GRCh38.p7 | 8:55909938 | TTTTGAAAAATATGT[A/G]TTCATGTTCTTTGCC | 4067 |
rs79308980 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | LYN | GRCh38.p7 | 8:55912400 | ACTATACCATGCCTG[C/T]GCTTAAGTAGTTTTT | 4067 |
rs79370872 | snp | A/G | 0.454423 | 0.143914 | intron-variant | LYN | GRCh38.p7 | 8:55911259 | TACGTGTGTGTGTGT[A/G]TATATATATATATAT | 4067 |
rs79408978 | snp | A/T | 0.0325976 | 0.123435 | intron-variant | LYN | GRCh38.p7 | 8:56008951 | AACTACAGACAAGTG[A/T]CCTTCAGATTAACTG | 4067 |
rs79412043 | snp | A/T | 0.0984431 | 0.198823 | intron-variant | LYN | GRCh38.p7 | 8:55966433 | AATGCAATGGTGCGA[A/T]CTCAGCTCACTGCAA | 4067 |
rs79474730 | snp | A/C | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55919028 | CTGTCTCTACAAAAA[A/C]AAAAAAAAAAAAAAA | 4067 |
rs79486848 | snp | A/G | 0.149999 | 0.229128 | utr-variant-5-prime | LYN | GRCh38.p7 | 8:55877812 | TGATCACTGCCTTCT[A/G]TGCTCAATTTAGAGA | 4067 |
rs79490546 | snp | C/T | 0.100944 | 0.200705 | intron-variant | LYN | GRCh38.p7 | 8:55935025 | TGCCCACACCATGGA[C/T]GGAAGCAGCTCCACG | 4067 |
rs79520241 | snp | C/G | 0.0471551 | 0.14613 | intron-variant | LYN | GRCh38.p7 | 8:55939535 | GCAGGAACGCAGTGG[C/G]GGGGGGACAGGGGAT | 4067 |
rs79522141 | snp | C/T | 0.122411 | 0.214991 | intron-variant | LYN | GRCh38.p7 | 8:55926000 | ATAAAACTTTTTATC[C/T]TGTTTTATAAAAATT | 4067 |
rs79594160 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | LYN | GRCh38.p7 | 8:55945073 | ATATGACAAAATGCA[C/T]GCTATGGATTGATTA | 4067 |
rs79623648 | snp | G/T | | | intron-variant | LYN | GRCh38.p7 | 8:55902470 | GTAGCTGGAATTACA[G/T]GTGCGCTCCACAACG | 4067 |
rs79634012 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | LYN | GRCh38.p7 | 8:55878639 | TTTCTCCATAGGATT[C/G]TTGATAGGTTTCAAT | 4067 |
rs79726138 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | LYN | GRCh38.p7 | 8:55901776 | GATGTGGCTAGGAAC[C/T]GGCTCCCAGCTGAAT | 4067 |
rs79765501 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | LYN | GRCh38.p7 | 8:55901344 | TTTAAGCAAAACCCC[A/G]GTGTTCTCTTGTCTG | 4067 |
rs79779650 | snp | A/T | | | intron-variant | LYN | GRCh38.p7 | 8:55882221 | CCAATCCAGAAGACC[A/T]ACATTATTTTAGAGT | 4067 |
rs79842493 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | LYN | GRCh38.p7 | 8:55949638 | GTATGCAGTGTGTAC[A/G]GATCAAGTCAGCGTA | 4067 |
rs79877474 | snp | A/C | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55997161 | AGTGAGACTGTCTCA[A/C]AAAAAAAAAAAAAAG | 4067 |
rs79904136 | snp | A/G | 0.0142736 | 0.0832652 | utr-variant-3-prime | LYN | GRCh38.p7 | 8:56010545 | TATACATAGCATGAC[A/G]TTTCTTTGTGCTTTG | 4067 |
rs79939821 | snp | G/T | 0.0737376 | 0.17729 | intron-variant | LYN | GRCh38.p7 | 8:55965789 | GAGTTTTGTTTTGTT[G/T]TTTTTGGTCTTGAAT | 4067 |
rs79946269 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | LYN | GRCh38.p7 | 8:55901713 | GAAGCTACAGCAGCA[A/C]TGCTCTATCCTAGAC | 4067 |
rs79976542 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | LYN | GRCh38.p7 | 8:55887146 | TAATATGAAAAATTT[A/T]TTTTCAAAAGCTGAA | 4067 |
rs80005936 | snp | A/C | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55934225 | AGCGAGATCCGTCTC[A/C]AAAAAAAAGAAGGAG | 4067 |
rs80034178 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LYN | GRCh38.p7 | 8:55906095 | CTGTTAAGTCAGAGG[C/G]CTGGGATGGTGAGGT | 4067 |
rs80037740 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | LYN | GRCh38.p7 | 8:55945954 | TCTCCATCCTGCTGC[C/T]GCTGGTGTTTGCTTT | 4067 |
rs80097288 | snp | G/T | 0.095934 | 0.196885 | intron-variant | LYN | GRCh38.p7 | 8:55899338 | GAACCCAAGTCAGCC[G/T]GACCCCTAAACTGAT | 4067 |
rs80106623 | snp | A/T | 0.00716266 | 0.059414 | upstream-variant-2KB, utr-variant-5-prime | LYN | GRCh38.p7 | 8:55878329 | CTCAGGTAAGCCTGA[A/T]GATGCTTTGTTCCTT | 4067 |
rs80121350 | snp | C/T | | | intron-variant | LYN | GRCh38.p7 | 8:55949767 | TTTTTAATAGCTTTA[C/T]TGAGAATTCACAATA | 4067 |
rs80218232 | snp | A/C | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55987408 | TGAGACTTCATCTCA[A/C]AAAAAAAAAAAAAAA | 4067 |
rs80252396 | snp | A/T | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55927747 | AGACTGAGGCAGGAG[A/T]ATTTTTTGAACCTGG | 4067 |
rs111237452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYN | GRCh38.p7 | 8:55941183 | AGGCCCCCCACCCCA[C/T]TCCACCTTGCACACT | 4067 |
rs111239271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYN | GRCh38.p7 | 8:55911552 | CGTAGGGGCAGCAGG[C/T]GGAAATGTACATTCA | 4067 |
rs111241896 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | LYN | GRCh38.p7 | 8:55904539 | CATGGAATTATGATG[C/T]CACACAAAATAATTT | 4067 |
rs111253430 | snp | C/G | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55881364 | AACTGGTGGGCTACA[C/G]GGATGTTTTCTCTGT | 4067 |
rs111282776 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LYN | GRCh38.p7 | 8:55943050 | GCTGGACTAGAAATA[G/T]TTTATGAGTGATGTG | 4067 |
rs111286775 | snp | A/G | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55946238 | CGCTCCCTTCCTGCC[A/G]CCCACAGCAAGTGAT | 4067 |
rs111289256 | snp | A/T | 0.0232847 | 0.105357 | intron-variant | LYN | GRCh38.p7 | 8:55987687 | TCCCAAAGTGCTGGG[A/T]TTATAGGCATGAGCC | 4067 |
rs111295560 | in-del | -/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | LYN | GRCh38.p7 | 8:55922659 | GTAATCCCAGCTATT[-/G]GGGGAGCTGAGGCAG | 4067 |
rs111296805 | snp | C/T | 0.163892 | 0.234703 | intron-variant | LYN | GRCh38.p7 | 8:55892188 | AGCATTTTAGAAGGC[C/T]GAGGCAGATGGATCA | 4067 |
rs111298995 | in-del | -/TA | 0.267364 | 0.249396 | intron-variant | LYN | GRCh38.p7 | 8:55942332 | ATGTATATATATGTG[-/TA]TATATATATGTGTAT | 4067 |
rs111300731 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LYN | GRCh38.p7 | 8:55970708 | GTACAGAGGTGAAGC[A/C]CCTCACCTAAGGTAG | 4067 |
rs111304364 | snp | A/G | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55947917 | TTTTCCTTTTAAGTC[A/G]GTCTGTGAGCACACT | 4067 |
rs111304538 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | LYN | GRCh38.p7 | 8:55995860 | CGGAAGTGAAATACT[A/G]GACTGAATAGTCTTT | 4067 |
rs111313187 | snp | C/T | 0.143284 | 0.226079 | intron-variant | LYN | GRCh38.p7 | 8:55934182 | AGTGAGCCGAGATTG[C/T]GCCATTGCACTCCAG | 4067 |
rs111323958 | snp | A/T | 0.0581099 | 0.160244 | intron-variant | LYN | GRCh38.p7 | 8:55953493 | CTCTACTAAAAAATA[A/T]AAAAACTAGCTGGGC | 4067 |
rs111342382 | snp | A/G | 0.0174175 | 0.0916809 | utr-variant-3-prime | LYN | GRCh38.p7 | 8:56010653 | CTTTCCCAGATTTCA[A/G]TGATTTTTTTCCCCC | 4067 |
rs111353190 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LYN | GRCh38.p7 | 8:55880425 | CCGCGTGTCCTTCCC[G/T]GTGAGGGCCCGAGGG | 4067 |
rs111386305 | snp | C/G | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:56000863 | GTTTAAATCTTTCTC[C/G]TATTCAAAAAATATT | 4067 |
rs111441103 | snp | A/G | 0.0509478 | 0.151255 | intron-variant | LYN | GRCh38.p7 | 8:55925119 | TGAGCCACCGTGCCC[A/G]GCCTCTTTTTTTGTT | 4067 |
rs111458273 | snp | A/G | 0.142609 | 0.225759 | intron-variant | LYN | GRCh38.p7 | 8:55927708 | TGTGTGGTGGCGGGT[A/G]CCTGTAATGCCCAGC | 4067 |
rs111551315 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | LYN | GRCh38.p7 | 8:55936174 | GCTTGAACCAGTCTT[A/G]GACCTAATTTGAAAC | 4067 |
rs111592867 | snp | C/T | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55959000 | GGCTGGATCCTGTAA[C/T]TCTTCTATCTCTAAA | 4067 |
rs111611540 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | LYN | GRCh38.p7 | 8:55999925 | GCAGTGAGCTGAGAT[C/T]GCGCCATTCCACTCC | 4067 |
rs111627561 | snp | A/G | 0.141596 | 0.225274 | intron-variant | LYN | GRCh38.p7 | 8:55934024 | CAAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 4067 |
rs111635714 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | LYN | GRCh38.p7 | 8:55960160 | AAATGGGTAAATGAC[A/G]TGGTATATGAATTAT | 4067 |
rs111647306 | snp | C/T | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55887575 | ATATATATATATATA[C/T]ACACACACACACACA | 4067 |
rs111730117 | snp | C/T | 0.155987 | 0.23165 | intron-variant | LYN | GRCh38.p7 | 8:55894714 | ATTTTTTTGTATTTT[C/T]AGTAGAGACGGGGTT | 4067 |
rs111743735 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LYN | GRCh38.p7 | 8:55882832 | CAGGCTTGGTTAAGC[A/G]GTACCATTAGGAGTA | 4067 |
rs111765573 | in-del | -/A | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55905410 | GTGAAACTCCGTCTC[-/A]AAAAAAAAGAAAGAA | 4067 |
rs111778968 | snp | G/T | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55967594 | GTGCTAGGATTACAG[G/T]CATGAGCACCCAGCC | 4067 |
rs111791264 | snp | A/G | 0.117886 | 0.21224 | intron-variant | LYN | GRCh38.p7 | 8:55997896 | GAGACCATCCTGGCT[A/G]ACATGGTGAAACCCC | 4067 |
rs111797259 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | LYN | GRCh38.p7 | 8:55934095 | GCCAGGCATGGTGGC[A/G]AGCGCCTGTAGTCCC | 4067 |
rs111848943 | in-del | -/CAAA | 0.0520825 | 0.152737 | intron-variant | LYN | GRCh38.p7 | 8:56006270 | AAATTTGTCCTGCTG[-/CAAA]CAAACACTCACCTTG | 4067 |
rs111849184 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | LYN | GRCh38.p7 | 8:55997881 | CGAGGTCAGGAGATC[C/G]AGACCATCCTGGCTA | 4067 |
rs111850394 | snp | A/T | | | intron-variant | LYN | GRCh38.p7 | 8:55931180 | ATATTATATTTTAAA[A/T]TATAATATGTAACTC | 4067 |
rs111857708 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LYN | GRCh38.p7 | 8:55896132 | AGTTTTAGCTAGACG[C/T]GGTGGCATGCCCCTG | 4067 |
rs111880687 | snp | C/G | 0.148996 | 0.228688 | intron-variant | LYN | GRCh38.p7 | 8:55951597 | TTGAGCCCAAGAGGT[C/G]GAGGCTGCAGTTAGC | 4067 |
rs111903948 | snp | A/G/T | 0.0275645 | 0.114116 | intron-variant | LYN | GRCh38.p7 | 8:55942700 | TGAGGCAGGAGAATC[A/G/T]CTTGAACCTGGGAAG | 4067 |
rs111912929 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | LYN | GRCh38.p7 | 8:55962421 | TGGTGAGATGCATCC[A/G]TGCTTTTGGGTGTGA | 4067 |
rs111924341 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | LYN | GRCh38.p7 | 8:55944805 | TTTTTAAATGATGAA[C/T]AAAGATGTCCTTTAT | 4067 |
rs111951441 | in-del | -/AG/AGAGAG/AGAGAGAGAG | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55939462 | CCTTTTCCCAAGAGA[-/AG/AGAGAG/AGAGAGAGAG]AGAGAGAGAGAGAGA | 4067 |
rs111953180 | snp | A/G | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:56003687 | TCAAAAAAAAAAAAA[A/G]AAGAAGTCATATCAT | 4067 |
rs112004572 | snp | C/T | | | intron-variant | LYN | GRCh38.p7 | 8:55902335 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTGAGAT | 4067 |
rs112045629 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | LYN | GRCh38.p7 | 8:55882232 | GACCTACATTATTTT[A/C]GAGTCATTGGTGTTA | 4067 |
rs112090436 | in-del | -/CTC | 0 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55953748 | TTGGACACTATAAGG[-/CTC]CTAGTGTTCAACTTT | 4067 |
rs112100083 | snp | A/C | 0.0733688 | 0.176922 | intron-variant | LYN | GRCh38.p7 | 8:55898400 | TTCAAGCAATCCTCC[A/C]ATCTCAGCCTCCCAA | 4067 |
rs112105166 | snp | G/T | 0.149665 | 0.228982 | intron-variant | LYN | GRCh38.p7 | 8:55903808 | TACTTGAGCCCAGGA[G/T]TTTGACACCAGCCTG | 4067 |
rs112108402 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | LYN | GRCh38.p7 | 8:55922385 | ATGAGCCACCACACC[A/T]GGCTGACATCACAAT | 4067 |
rs112143439 | snp | A/C | | | intron-variant | LYN | GRCh38.p7 | 8:56002082 | GGTCAGGAGTTCGAG[A/C]CCAGCCTGGCCAACA | 4067 |
rs112157637 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | LYN | GRCh38.p7 | 8:55934785 | CTTCCCACCTCACCC[A/C]CCTTTCCCAATTGAC | 4067 |
rs112159623 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | LYN | GRCh38.p7 | 8:55968844 | CTTGACCAAGGCTAC[A/C/G]CGTAAGGCTGGTACT | 4067 |
rs112164934 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | LYN | GRCh38.p7 | 8:55957339 | TTCCCCAATTTTAAT[A/C]ATAAAACAGAGCCAT | 4067 |
rs112181335 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | LYN | GRCh38.p7 | 8:55910086 | ATATACTTTCTCCCA[C/T]TCTGCAGGTTGTCGG | 4067 |
rs112202706 | snp | C/G | 0.0345262 | 0.126772 | intron-variant | LYN | GRCh38.p7 | 8:55979688 | CTGAGGTTCCCATCT[C/G]AGGCCTCCACCCAGC | 4067 |
rs112206062 | snp | A/T | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55961970 | TTTTGCCACTTTTGT[A/T]TATGGGGATGTATGC | 4067 |
rs112284736 | snp | A/C | 0.021333 | 0.101051 | intron-variant | LYN | GRCh38.p7 | 8:55894206 | TTATTTTATTTTTTA[A/C]TTTTTATTATTTTAG | 4067 |
rs112304696 | snp | A/G/T | 0.00716266 | 0.059414 | intron-variant | LYN | GRCh38.p7 | 8:55898375 | CTCACTGCAACCTCC[A/G/T]CCTTCCGTGTTCAAG | 4067 |
rs112330763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYN | GRCh38.p7 | 8:55938336 | TAACCAAATTCTCTA[C/T]GCATAAAATATGTCT | 4067 |
rs112353231 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | LYN | GRCh38.p7 | 8:55900775 | TTCAGTATGTATCTC[A/T]TACTTTTCTTTTGCT | 4067 |
rs112366578 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | LYN | GRCh38.p7 | 8:55944089 | GCGAGAGTCTCCAAA[A/G]AAAAAGGAAGTGGAG | 4067 |
rs112408594 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | LYN | GRCh38.p7 | 8:55997912 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 4067 |
rs112415811 | snp | C/T | 0.124837 | 0.216412 | intron-variant | LYN | GRCh38.p7 | 8:55925030 | TATTTTTAGTAGAGA[C/T]GGGATTTCACCATGT | 4067 |
rs112421369 | snp | A/T | | | intron-variant | LYN | GRCh38.p7 | 8:55951754 | TCATGAAGAAAGAAA[A/T]TGGTATGTTGGCAAG | 4067 |
rs112427676 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | LYN | GRCh38.p7 | 8:55929709 | AGTGGGTAGAGGCCA[A/G]GGATGCTGCTAAGTA | 4067 |
rs112429473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LYN | GRCh38.p7 | 8:55974733 | GATGTGTTAGACGCT[C/T]ATATTCCACCTCAAG | 4067 |
rs112429665 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | LYN | GRCh38.p7 | 8:55987668 | TGATCCACCCACCTC[A/G]TCCTCCCAAAGTGCT | 4067 |
rs112431000 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | LYN | GRCh38.p7 | 8:55939590 | GCTCAGTCAGGGCTC[C/G]GTCCGTGCTGGGAGG | 4067 |
rs112456008 | snp | A/G | 0.234692 | 0.249531 | intron-variant | LYN | GRCh38.p7 | 8:55934055 | ATATGGTGAAACCCC[A/G]TCTTTACTAAAAGTA | 4067 |
rs112470212 | snp | C/G | | | intron-variant | LYN | GRCh38.p7 | 8:56002322 | TACTCGGGAGGCTGG[C/G]GCAGGAGAATGGCAT | 4067 |
rs112497839 | in-del | -/C | 0.198014 | 0.244535 | intron-variant | LYN | GRCh38.p7 | 8:55936976 | TTTATCCCTTTTCTA[-/C]CCCCCACGTCTTTTG | 4067 |
rs112576994 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | LYN | GRCh38.p7 | 8:55983074 | TTTGCCCTCATGTCC[A/G]CACAACAGCTGTGAC | 4067 |
rs112591757 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | LYN | GRCh38.p7 | 8:56003480 | GACCAGCCTGGACAA[C/T]ATGGCCAAACCCTGT | 4067 |
rs112607389 | snp | A/G | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55943032 | CCTAACCTTAGAGAA[A/G]TAGCTGGACTAGAAA | 4067 |
rs112654600 | in-del | -/T | 0.00755907 | 0.0610114 | intron-variant | LYN | GRCh38.p7 | 8:55907302 | TTGAATCTCAAAAAC[-/T]TTTTTTTCACCTATA | 4067 |
rs112676659 | snp | A/G | 0.039522 | 0.134904 | intron-variant | LYN | GRCh38.p7 | 8:56009584 | TGGTCTTTCCCCTAT[A/G]CTAGTCTGTGTTCTA | 4067 |
rs112687590 | snp | C/T | 0.5 | 0 | intron-variant | LYN | GRCh38.p7 | 8:55950189 | AGGCATTTTGGTTGT[C/T]TCTACTTTTTGCTTT | 4067 |
rs112699673 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | LYN | GRCh38.p7 | 8:55920123 | TGGGCTGTAAATATA[A/G]TAAAATAATTCAGCA | 4067 |
rs112705451 | snp | C/G | | | intron-variant | LYN | GRCh38.p7 | 8:55978850 | AGCCAAGCCCTTGGC[C/G]TCTCTCCCTCTTCCT | 4067 |
rs112710277 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | LYN | GRCh38.p7 | 8:55933411 | ATTCCAAACAGTCCC[A/G]CAATAAGTATTCTCT | 4067 |
rs112725195 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | LYN | GRCh38.p7 | 8:55999709 | GGGCATGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 4067 |
rs112748159 | in-del | -/T | 0.330482 | 0.236691 | intron-variant | LYN | GRCh38.p7 | 8:55947980 | TTTTCTTTAAAACAA[-/T]TTTTTTTTTTTGAGA | 4067 |
rs112754158 | snp | A/G | | | intron-variant | LYN | GRCh38.p7 | 8:55888757 | TTGTTTTGTTTTTGA[A/G]ACAGAGTCTCACTCT | 4067 |
rs112774305 | snp | C/G | | | intron-variant | LYN | GRCh38.p7 | 8:55880167 | GGGTGCAGGGGCCGC[C/G]GCTGTGCCACCAGCC | 4067 |
rs112775774 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | LYN | GRCh38.p7 | 8:55944014 | TTTGAACCAGGACCC[A/G]GGAGGGAGAGGTTGC | 4067 |
rs112779890 | snp | A/G | 0.142947 | 0.22592 | intron-variant | LYN | GRCh38.p7 | 8:55928295 | GGACTATAGGCAAGC[A/G]CCACCACGCCCGGCT | 4067 |