Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1253570532 | 0.925 | 0.080 | 21 | 34792289 | missense variant | G/A | snv | 7.0E-06 | 2 | ||
rs772889171 | 0.925 | 0.080 | 21 | 34834487 | missense variant | G/A | snv | 4.0E-06 | 2 | ||
rs17576 | 0.557 | 0.760 | 20 | 46011586 | missense variant | A/G | snv | 0.39 | 0.36 | 73 | |
rs12979860 | 0.547 | 0.520 | 19 | 39248147 | intron variant | C/T | snv | 0.39 | 84 | ||
rs318699 | 0.882 | 0.080 | 19 | 11390564 | intron variant | A/G | snv | 0.73 | 3 | ||
rs17849241 | 0.925 | 0.080 | 17 | 78358688 | missense variant | G/C;T | snv | 4.1E-06; 2.1E-04 | 3 | ||
rs267606870 | 0.763 | 0.280 | 15 | 90088703 | missense variant | G/A;C | snv | 11 | |||
rs775387828 | 0.851 | 0.200 | 12 | 54293083 | missense variant | G/A | snv | 2.2E-05 | 7.0E-06 | 7 | |
rs1188383936 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 102 | ||
rs754190776 | 0.925 | 0.080 | 11 | 5253350 | missense variant | G/A | snv | 8.0E-06 | 2 | ||
rs77375493 | 0.458 | 0.760 | 9 | 5073770 | missense variant | G/A;T | snv | 3.5E-04 | 187 | ||
rs12342421 | 0.851 | 0.080 | 9 | 5065750 | intron variant | G/C | snv | 0.23 | 5 | ||
rs10815148 | 0.882 | 0.080 | 9 | 5057284 | intron variant | T/A | snv | 0.33 | 3 | ||
rs10974947 | 0.882 | 0.080 | 9 | 5072846 | intron variant | G/A | snv | 0.23 | 3 | ||
rs121912473 | 0.925 | 0.080 | 9 | 5070026 | missense variant | AA/TT | mnv | 3 | |||
rs12339666 | 0.925 | 0.080 | 9 | 5063296 | intron variant | G/T | snv | 0.34 | 3 | ||
rs4495487 | 0.925 | 0.080 | 9 | 5072798 | intron variant | T/C | snv | 0.23 | 3 | ||
rs1200469268 | 0.925 | 0.080 | 9 | 104830968 | missense variant | C/A | snv | 7.0E-06 | 2 | ||
rs3808850 | 0.925 | 0.080 | 9 | 4983311 | upstream gene variant | T/A;C | snv | 2 | |||
rs7046736 | 0.925 | 0.080 | 9 | 5015732 | intron variant | C/A | snv | 0.39 | 2 | ||
rs11999802 | 1.000 | 0.080 | 9 | 5189773 | upstream gene variant | T/G | snv | 0.33 | 1 | ||
rs773475680 | 1.000 | 0.080 | 9 | 130884139 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
rs777342222 | 1.000 | 0.080 | 7 | 55155925 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
rs361525 | 0.562 | 0.760 | 6 | 31575324 | upstream gene variant | G/A | snv | 4.6E-02 | 62 | ||
rs9376092 | 0.851 | 0.120 | 6 | 135106006 | upstream gene variant | C/A | snv | 0.24 | 10 |