Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs397507444 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 306 | |||
rs2910164 | 0.447 | 0.880 | 5 | 160485411 | mature miRNA variant | C/G | snv | 0.71; 4.1E-06 | 0.70 | 193 | |
rs1801131 | 0.535 | 0.840 | 1 | 11794419 | missense variant | T/G | snv | 0.29 | 0.26 | 93 | |
rs234709 | 0.827 | 0.200 | 21 | 43066854 | intron variant | C/T | snv | 7 | |||
rs4752028 | 0.807 | 0.200 | 10 | 117075480 | intron variant | C/T | snv | 0.73 | 6 | ||
rs2124459 | 0.827 | 0.200 | 21 | 43055604 | 3 prime UTR variant | T/C | snv | 0.36 | 5 | ||
rs7078160 | 0.851 | 0.120 | 10 | 117068049 | intron variant | G/A | snv | 0.19 | 4 | ||
rs4938016 | 0.925 | 0.120 | 11 | 113399293 | missense variant | G/A;C;T | snv | 1.7E-04; 0.64; 2.0E-03 | 2 | ||
rs234705 | 0.925 | 0.120 | 21 | 43063662 | intron variant | C/T | snv | 2 | |||
rs1076562 | 0.925 | 0.120 | 11 | 113425286 | intron variant | A/G | snv | 0.65 | 2 | ||
rs2855530 | 1.000 | 0.120 | 14 | 53955199 | non coding transcript exon variant | G/C | snv | 0.50 | 1 |