Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057519721 | 0.882 | 0.120 | 9 | 5078360 | missense variant | A/G | snv | 4 | |||
rs10974944 | 0.882 | 0.160 | 9 | 5070831 | intron variant | C/G | snv | 0.25 | 4 | ||
rs121913520 | 1.000 | 0.080 | 4 | 54727443 | missense variant | G/A | snv | 4 | |||
rs778767225 | 0.851 | 0.200 | 14 | 102231805 | missense variant | C/A | snv | 2.4E-05 | 7.0E-06 | 4 | |
rs2201862 | 0.925 | 0.080 | 3 | 168930251 | downstream gene variant | T/C | snv | 0.63 | 3 | ||
rs562533120 | 0.882 | 0.080 | 6 | 134966397 | missense variant | A/C | snv | 8.0E-06 | 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 | ||
rs121912473 | 0.925 | 0.080 | 9 | 5070026 | missense variant | AA/TT | mnv | 3 | |||
rs121913504 | 0.882 | 0.080 | 19 | 17837200 | missense variant | G/A | snv | 3 | |||
rs17292650 | 0.882 | 0.120 | 1 | 43338136 | missense variant | G/T | snv | 3.5E-03 | 1.4E-02 | 3 | |
rs17849241 | 0.925 | 0.080 | 17 | 78358688 | missense variant | G/C;T | snv | 4.1E-06; 2.1E-04 | 3 | ||
rs1259653415 | 1.000 | 0.080 | 3 | 196071416 | missense variant | T/C | snv | 7.0E-06 | 3 | ||
rs4858647 | 0.925 | 0.080 | 3 | 24749884 | intron variant | C/A;G;T | snv | 2 | |||
rs1200469268 | 0.925 | 0.080 | 9 | 104830968 | missense variant | C/A | snv | 7.0E-06 | 2 | ||
rs529311209 | 0.925 | 0.120 | 22 | 40409754 | missense variant | G/A;C;T | snv | 3.3E-05; 8.2E-06 | 2 | ||
rs3733609 | 1.000 | 0.080 | 4 | 105269705 | missense variant | T/A;C | snv | 6.4E-06; 3.4E-02 | 2 | ||
rs12340895 | 1.000 | 0.080 | 9 | 5076691 | intron variant | C/A;G | snv | 1 | |||
rs59384377 | 1.000 | 0.080 | 9 | 5005034 | intron variant | A/T | snv | 0.26 | 1 | ||
rs764634461 | 1.000 | 0.080 | 9 | 5072516 | missense variant | T/G | snv | 1.2E-05 | 2.8E-05 | 1 | |
rs1057519752 | 1.000 | 0.080 | 1 | 43349307 | missense variant | A/C;G;T | snv | 1 | |||
rs1441084781 | 1.000 | 0.080 | 9 | 117712543 | missense variant | G/A;T | snv | 4.0E-06 | 1 |