Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 24 | ||
rs35747 | 12 | 102518780 | intergenic variant | G/A | snv | 0.70 | 3 | ||||
rs11191580 | 0.827 | 0.040 | 10 | 103146454 | intron variant | T/C | snv | 7.9E-02 | 10 | ||
rs2967951 | 5 | 10463995 | intron variant | C/T | snv | 0.19 | 1 | ||||
rs3934834 | 1 | 1070426 | downstream gene variant | C/T | snv | 0.21 | 1 | ||||
rs12229654 | 0.763 | 0.320 | 12 | 110976657 | intergenic variant | T/G | snv | 4.8E-03 | 7 | ||
rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 21 | |
rs308971 | 3 | 12075120 | intron variant | G/A | snv | 0.82 | 3 | ||||
rs1801282 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 5 | |
rs7973683 | 12 | 123964676 | intron variant | C/A | snv | 0.39 | 1 | ||||
rs4836133 | 0.925 | 0.160 | 5 | 124996410 | intron variant | C/A;G;T | snv | 1 | |||
rs867559 | 9 | 126703046 | non coding transcript exon variant | A/G | snv | 0.26 | 1 | ||||
rs2745353 | 6 | 127131790 | intron variant | C/T | snv | 0.55 | 3 | ||||
rs2275215 | 6 | 129540247 | intron variant | T/C | snv | 0.35 | 1 | ||||
rs1542829 | 3 | 130418627 | intron variant | G/A | snv | 8.0E-02 | 1 | ||||
rs1106683 | 7 | 131768766 | intergenic variant | G/A | snv | 0.14 | 1 | ||||
rs2890652 | 2 | 142202362 | intergenic variant | T/C | snv | 0.21 | 1 | ||||
rs7708584 | 5 | 154163906 | intron variant | A/G | snv | 0.58 | 1 | ||||
rs4691380 | 4 | 156798972 | intron variant | C/T | snv | 0.45 | 4 | ||||
rs7607980 | 1.000 | 0.080 | 2 | 164694691 | missense variant | T/C | snv | 0.11 | 0.13 | 7 | |
rs633715 | 1.000 | 0.080 | 1 | 177883445 | intron variant | T/C | snv | 0.17 | 5 | ||
rs516636 | 1 | 177886382 | intron variant | C/A | snv | 0.17 | 1 | ||||
rs574367 | 1 | 177904075 | intron variant | G/T | snv | 0.16 | 1 | ||||
rs543874 | 1.000 | 0.080 | 1 | 177920345 | upstream gene variant | A/G | snv | 0.21 | 8 | ||
rs591120 | 1 | 177933618 | missense variant | G/A;C | snv | 4.0E-06; 0.42 | 1 |