Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7903146 | 0.554 | 0.680 | 10 | 112998590 | intron variant | C/G;T | snv | 93 | |||
rs12255372 | 0.667 | 0.480 | 10 | 113049143 | intron variant | G/A;T | snv | 28 | |||
rs13266634 | 0.724 | 0.480 | 8 | 117172544 | missense variant | C/A;T | snv | 0.29 | 23 | ||
rs4506565 | 0.790 | 0.280 | 10 | 112996282 | intron variant | A/G;T | snv | 22 | |||
rs651007 | 0.851 | 0.160 | 9 | 133278431 | upstream gene variant | T/A;C | snv | 22 | |||
rs174576 | 0.851 | 0.200 | 11 | 61836038 | intron variant | C/A;T | snv | 14 | |||
rs7756992 | 0.827 | 0.240 | 6 | 20679478 | intron variant | A/G;T | snv | 12 | |||
rs1387153 | 0.807 | 0.200 | 11 | 92940662 | downstream gene variant | C/G;T | snv | 10 | |||
rs4607517 | 0.882 | 0.080 | 7 | 44196069 | intron variant | G/A;C | snv | 8 | |||
rs9368222 | 1.000 | 0.080 | 6 | 20686765 | intron variant | C/A;T | snv | 8 | |||
rs10830962 | 0.851 | 0.160 | 11 | 92965261 | upstream gene variant | C/A;G;T | snv | 7 | |||
rs13023194 | 0.925 | 0.120 | 2 | 27744393 | intergenic variant | G/A;C | snv | 4 | |||
rs4665965 | 0.925 | 0.120 | 2 | 27313513 | intron variant | T/A;C | snv | 4 | |||
rs853789 | 2 | 168944978 | intron variant | A/G;T | snv | 0.75 | 4 | ||||
rs1783598 | 1.000 | 0.080 | 11 | 73140418 | intron variant | C/G;T | snv | 3 | |||
rs2018860 | 0.925 | 0.120 | 15 | 98715481 | intron variant | A/C;G;T | snv | 3 | |||
rs7034200 | 1.000 | 0.080 | 9 | 4289050 | intron variant | C/A;G | snv | 3 | |||
rs8004664 | 0.925 | 0.080 | 14 | 89568628 | intron variant | G/A;C | snv | 3 | |||
rs10278336 | 7 | 44205764 | intron variant | A/C;G | snv | 2 | |||||
rs10747083 | 12 | 132465032 | downstream gene variant | G/A;T | snv | 2 | |||||
rs11195502 | 10 | 111279909 | intergenic variant | C/A;G;T | snv | 2 | |||||
rs11715915 | 3 | 49417897 | synonymous variant | C/A;T | snv | 0.28 | 2 | ||||
rs117911989 | 7 | 131285034 | intron variant | G/A;C | snv | 2 | |||||
rs1974620 | 1.000 | 0.080 | 7 | 15025842 | intergenic variant | C/A;T | snv | 2 | |||
rs2166706 | 1.000 | 0.080 | 11 | 92958366 | intergenic variant | T/A;C | snv | 2 |