Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1466524306 | 1.000 | 0.040 | 13 | 99295133 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
rs750610248 | 0.882 | 0.200 | 14 | 99175513 | missense variant | A/C;G | snv | 4.1E-06 | 1 | ||
rs786205156 | 1.000 | 2 | 99162492 | missense variant | A/G | snv | 4.0E-06 | 1 | |||
rs137973334 | 1.000 | 2 | 99162249 | missense variant | C/G;T | snv | 1.2E-04; 4.0E-06 | 1 | |||
rs767568897 | 1.000 | 2 | 99162169 | missense variant | C/G;T | snv | 8.0E-06; 8.8E-05 | 1 | |||
rs142573758 | 1.000 | 0.080 | 4 | 991538 | missense variant | C/T | snv | 5.6E-04 | 6.0E-04 | 1 | |
rs113605875 | 0.882 | 0.120 | 9 | 99149253 | missense variant | G/A;C;T | snv | 1 | |||
rs111426349 | 0.882 | 0.120 | 9 | 99149252 | missense variant | C/A;T | snv | 4.0E-06 | 1 | ||
rs121918711 | 1.000 | 0.120 | 9 | 99146553 | missense variant | A/G | snv | 1 | |||
rs121918710 | 1.000 | 0.120 | 9 | 99142683 | missense variant | T/G | snv | 1 | |||
rs111854391 | 0.716 | 0.280 | 9 | 99138006 | stop gained | C/A;T | snv | 4.0E-06 | 1 | ||
rs121918712 | 1.000 | 0.120 | 9 | 99137883 | missense variant | C/T | snv | 1 | |||
rs757374917 | 9 | 99129005 | missense variant | C/T | snv | 1 | |||||
rs587776865 | 9 | 99128911 | missense variant | G/C | snv | 1 | |||||
rs387906696 | 9 | 99128891 | missense variant | A/G | snv | 8.0E-06 | 2.8E-05 | 1 | |||
rs139024319 | 1.000 | 0.080 | 4 | 991150 | missense variant | G/A | snv | 2.5E-04 | 1.6E-04 | 1 | |
rs148832260 | 1.000 | 0.080 | 4 | 989866 | missense variant | G/A | snv | 2.8E-04 | 3.1E-04 | 1 | |
rs1294404368 | 1.000 | 0.080 | 7 | 98981947 | missense variant | C/T | snv | 4.4E-06 | 1.4E-05 | 1 | |
rs753661271 | 1.000 | 0.080 | 7 | 98976613 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
rs528967912 | 1.000 | 0.080 | 7 | 98964724 | missense variant | C/T | snv | 1.6E-05 | 7.0E-06 | 1 | |
rs141802822 | 1.000 | 0.080 | 15 | 98957347 | missense variant | C/T | snv | 3.3E-04 | 6.8E-04 | 1 | |
rs782203759 | 1.000 | 0.080 | 7 | 98950120 | missense variant | G/A | snv | 2.4E-05 | 2.8E-05 | 1 | |
rs373632999 | 1.000 | 0.080 | 7 | 98949733 | missense variant | G/A | snv | 1.2E-05 | 4.2E-05 | 1 | |
rs587777730 | 1.000 | 3 | 9893310 | missense variant | A/G | snv | 8.0E-06 | 1.4E-05 | 1 | ||
rs587777728 | 1.000 | 3 | 9892955 | missense variant | C/T | snv | 1 |