Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3094122 | 1.000 | 0.120 | 6 | 30760583 | intron variant | T/G | snv | 0.21 | 1 | ||
rs3104402 | 1.000 | 0.120 | 6 | 32713899 | upstream gene variant | T/G | snv | 0.96 | 1 | ||
rs3842753 | 1.000 | 0.120 | 11 | 2159830 | missense variant | T/G | snv | 0.73 | 0.60 | 1 | |
rs4849135 | 1.000 | 0.120 | 2 | 110857502 | intron variant | T/G | snv | 0.67 | 1 | ||
rs7762619 | 1.000 | 0.120 | 6 | 31563533 | downstream gene variant | T/G | snv | 1.5E-02 | 1 | ||
rs928815 | 1.000 | 0.120 | 6 | 31563438 | downstream gene variant | T/G | snv | 0.65 | 1 | ||
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 81 | |
rs1063856 | 0.763 | 0.400 | 12 | 6044368 | missense variant | T/C;G | snv | 0.31 | 14 | ||
rs1332099 | 0.724 | 0.240 | 10 | 99538694 | downstream gene variant | T/C;G | snv | 14 | |||
rs9261290 | 0.807 | 0.280 | 6 | 30070870 | 3 prime UTR variant | T/C;G | snv | 5.2E-02; 7.2E-06 | 10 | ||
rs9273349 | 0.827 | 0.200 | 6 | 32658092 | upstream gene variant | T/C;G | snv | 6 | |||
rs1150752 | 0.882 | 0.240 | 6 | 32096949 | missense variant | T/C;G | snv | 5.9E-02 | 3 | ||
rs412657 | 0.882 | 0.240 | 6 | 32243308 | intergenic variant | T/C;G | snv | 3 | |||
rs7202877 | 0.882 | 0.160 | 16 | 75213347 | intergenic variant | T/C;G | snv | 3 | |||
rs2050189 | 0.925 | 0.200 | 6 | 32371870 | 5 prime UTR variant | T/C;G | snv | 0.18 | 2 | ||
rs272893 | 0.925 | 0.160 | 5 | 132327369 | missense variant | T/C;G | snv | 0.58; 4.0E-06 | 2 | ||
rs35795399 | 1.000 | 0.120 | 4 | 76021524 | 3 prime UTR variant | T/C;G | snv | 1 | |||
rs662 | 0.485 | 0.840 | 7 | 95308134 | missense variant | T/C | snv | 0.38 | 0.42 | 157 | |
rs1267969615 | 0.532 | 0.760 | 17 | 63490960 | missense variant | T/C | snv | 4.0E-06 | 100 | ||
rs3804100 | 0.633 | 0.720 | 4 | 153704257 | synonymous variant | T/C | snv | 9.0E-02 | 6.7E-02 | 36 | |
rs2104286 | 0.662 | 0.440 | 10 | 6057082 | intron variant | T/C | snv | 0.18 | 25 | ||
rs10811661 | 0.724 | 0.400 | 9 | 22134095 | intergenic variant | T/C | snv | 0.14 | 22 | ||
rs12976445 | 0.689 | 0.600 | 19 | 51693200 | non coding transcript exon variant | T/C | snv | 0.45 | 20 | ||
rs12232497 | 0.701 | 0.360 | 17 | 39883866 | intergenic variant | T/C | snv | 0.35 | 18 | ||
rs560887 | 0.827 | 0.120 | 2 | 168906638 | intron variant | T/C | snv | 0.79 | 0.80 | 18 |