Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7041 | 0.576 | 0.800 | 4 | 71752617 | missense variant | A/C;T | snv | 0.52; 4.0E-06 | 64 | ||
rs4588 | 0.597 | 0.720 | 4 | 71752606 | missense variant | G/A;T | snv | 1.6E-05; 0.25 | 53 | ||
rs12785878 | 0.677 | 0.520 | 11 | 71456403 | intron variant | G/A;T | snv | 25 | |||
rs3755967 | 0.925 | 0.080 | 4 | 71743681 | intron variant | C/A;T | snv | 6 | |||
rs12800438 | 1.000 | 0.080 | 11 | 71459957 | non coding transcript exon variant | G/A;T | snv | 5 | |||
rs1155563 | 0.925 | 0.080 | 4 | 71777771 | intron variant | T/A;C | snv | 4 | |||
rs10485165 | 6 | 88403098 | intron variant | C/G;T | snv | 3 | |||||
rs2302190 | 17 | 58507147 | missense variant | T/A;C | snv | 0.24 | 3 | ||||
rs4944062 | 11 | 71476248 | 3 prime UTR variant | G/A;T | snv | 2 | |||||
rs55665837 | 11 | 14473503 | intron variant | C/G;T | snv | 2 | |||||
rs6730714 | 2 | 222184302 | intergenic variant | G/A;T | snv | 2 | |||||
rs8018720 | 14 | 39086981 | missense variant | G/C;T | snv | 0.80; 1.1E-04 | 2 | ||||
rs843005 | 4 | 71750610 | intron variant | C/A;T | snv | 2 | |||||
rs182244780 | 11 | 14363985 | intron variant | G/A | snv | 6.0E-03 | 2 | ||||
rs117865811 | 11 | 14180763 | intron variant | A/G | snv | 6.3E-03 | 2 | ||||
rs117300835 | 11 | 15097429 | intergenic variant | G/A | snv | 7.6E-03 | 2 | ||||
rs117913124 | 11 | 14879385 | synonymous variant | G/A | snv | 1.7E-02 | 1.6E-02 | 2 | |||
rs719700 | 12 | 45635426 | intergenic variant | T/C | snv | 1.8E-02 | 2 | ||||
rs116970203 | 11 | 14855172 | intron variant | G/A | snv | 2.2E-02 | 2 | ||||
rs79666294 | 5 | 155047146 | regulatory region variant | C/T | snv | 2.2E-02 | 2 | ||||
rs12868495 | 13 | 34067425 | intergenic variant | G/A | snv | 2.3E-02 | 2 | ||||
rs148189294 | 4 | 71575200 | downstream gene variant | G/A | snv | 2.6E-02 | 2 | ||||
rs79761689 | 4 | 72005565 | intergenic variant | T/C | snv | 3.7E-02 | 2 | ||||
rs78862524 | 4 | 72305473 | intron variant | C/A | snv | 3.9E-02 | 3 | ||||
rs138485827 | 4 | 72166226 | intergenic variant | C/T | snv | 5.0E-02 | 2 |