Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11466023 | 0.827 | 0.320 | 16 | 3249586 | missense variant | G/A;T | snv | 1.5E-02; 4.0E-05 | 6 | ||
rs121908513 | 0.807 | 0.280 | 2 | 32116145 | missense variant | T/A | snv | 6 | |||
rs864622269 | 0.851 | 0.240 | 14 | 50628394 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 6 | |
rs886041761 | 0.925 | 0.200 | 1 | 110603902 | missense variant | C/T | snv | 6 | |||
rs104894490 | 0.827 | 0.240 | 15 | 22812252 | missense variant | G/A;C | snv | 5 | |||
rs119476046 | 0.827 | 0.240 | 14 | 50613343 | missense variant | C/T | snv | 5 | |||
rs2228044 | 0.882 | 0.240 | 5 | 55968325 | missense variant | C/G | snv | 0.13 | 0.21 | 5 | |
rs121434441 | 0.882 | 0.240 | 12 | 57569015 | missense variant | A/G | snv | 3 | |||
rs121908517 | 0.925 | 0.240 | 2 | 32063965 | missense variant | C/A | snv | 3.9E-04 | 6.2E-04 | 3 | |
rs121918262 | 0.882 | 0.240 | 2 | 86282216 | missense variant | G/A;T | snv | 4.0E-06 | 3 | ||
rs483352923 | 0.882 | 0.160 | 5 | 138441386 | missense variant | T/A | snv | 3 | |||
rs121908510 | 0.925 | 0.240 | 2 | 32136898 | missense variant | G/A | snv | 2 | |||
rs1331505548 | 0.925 | 0.200 | 2 | 148949891 | missense variant | A/G | snv | 2 | |||
rs145555213 | 0.925 | 0.160 | 6 | 5368994 | missense variant | G/A;T | snv | 4.0E-06; 4.0E-06 | 2 | ||
rs200154785 | 0.925 | 0.240 | 21 | 25997362 | missense variant | T/A | snv | 2 | |||
rs376971794 | 0.925 | 0.160 | 3 | 100728760 | missense variant | G/A | snv | 6.4E-05 | 3.5E-05 | 2 | |
rs483352925 | 0.925 | 0.160 | 5 | 138444447 | missense variant | T/A | snv | 2 | |||
rs768560449 | 1.000 | 0.160 | 2 | 86166521 | missense variant | A/G | snv | 8.1E-06 | 7.0E-06 | 2 | |
rs80338865 | 0.925 | 0.240 | 8 | 125061192 | missense variant | T/C | snv | 2 | |||
rs143129431 | 1.000 | 0.160 | 3 | 100748290 | missense variant | C/G | snv | 4.0E-06 | 1 | ||
rs757334523 | 1.000 | 0.160 | 19 | 10829132 | missense variant | C/T | snv | 1 | |||
rs762630964 | 1.000 | 0.160 | 2 | 32145007 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
rs989357227 | 1.000 | 0.160 | 3 | 100713749 | missense variant | C/T | snv | 1.6E-05 | 1 | ||
rs9463772 | 0.925 | 0.240 | 6 | 52246993 | non coding transcript exon variant | C/A;T | snv | 3 | |||
rs1800897 | 0.925 | 0.240 | 10 | 100809115 | synonymous variant | C/T | snv | 7.4E-02 | 0.13 | 2 |