Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7157599 | 0.925 | 0.040 | 14 | 100159565 | missense variant | C/T | snv | 0.73 | 0.76 | 2 | |
rs6712515 | 0.925 | 0.160 | 2 | 100190052 | intron variant | T/A;C | snv | 1 | |||
rs221780 | 1.000 | 0.040 | 7 | 100699412 | regulatory region variant | G/C;T | snv | 1 | |||
rs506597 | 0.882 | 0.040 | 7 | 100715797 | upstream gene variant | A/G | snv | 0.90 | 1 | ||
rs1734907 | 0.925 | 0.080 | 7 | 100717894 | upstream gene variant | A/G | snv | 0.84 | 2 | ||
rs13096071 | 1.000 | 0.040 | 3 | 101082799 | intergenic variant | T/A;C | snv | 1 | |||
rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 8 | ||
rs1035130 | 1.000 | 0.040 | 2 | 102384942 | synonymous variant | C/T | snv | 0.26 | 0.24 | 1 | |
rs6878284 | 0.925 | 0.040 | 5 | 102434022 | intron variant | C/T | snv | 0.64 | 1 | ||
rs1502844 | 1.000 | 0.040 | 5 | 102523613 | regulatory region variant | C/T | snv | 0.66 | 1 | ||
rs7085104 | 1.000 | 0.040 | 10 | 102869116 | intron variant | A/G | snv | 0.35 | 1 | ||
rs11191454 | 0.776 | 0.160 | 10 | 102900247 | intron variant | A/G | snv | 7.9E-02 | 1 | ||
rs1046778 | 0.851 | 0.160 | 10 | 102901727 | 3 prime UTR variant | T/C | snv | 0.30 | 1 | ||
rs7897654 | 1.000 | 0.040 | 10 | 102902701 | intron variant | T/C | snv | 0.30 | 1 | ||
rs7914558 | 0.851 | 0.040 | 10 | 103016151 | intron variant | G/A | snv | 0.40 | 2 | ||
rs11191580 | 0.827 | 0.040 | 10 | 103146454 | intron variant | T/C | snv | 7.9E-02 | 4 | ||
rs7775385 | 1.000 | 0.040 | 6 | 103198419 | intergenic variant | G/A;T | snv | 1 | |||
rs11191732 | 1.000 | 0.040 | 10 | 103572004 | intron variant | G/A | snv | 0.14 | 1 | ||
rs7341475 | 0.851 | 0.240 | 7 | 103764368 | intron variant | G/A | snv | 0.17 | 1 | ||
rs313327 | 1.000 | 0.040 | 12 | 104580243 | intron variant | C/T | snv | 0.75 | 1 | ||
rs9297357 | 0.851 | 0.040 | 8 | 105130105 | intron variant | C/G;T | snv | 1 | |||
rs11952719 | 1.000 | 0.040 | 5 | 106755127 | regulatory region variant | C/T | snv | 0.45 | 1 | ||
rs12871532 | 0.851 | 0.040 | 13 | 108016199 | intergenic variant | T/C | snv | 0.46 | 1 | ||
rs1379552 | 1.000 | 0.040 | 5 | 111643461 | intron variant | T/C | snv | 0.27 | 1 | ||
rs3782886 | 0.724 | 0.480 | 12 | 111672685 | synonymous variant | T/C | snv | 1.9E-02 | 5.9E-03 | 7 |