Source: UNIPROT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs137854470 | 1.000 | 0.160 | 15 | 48487425 | missense variant | C/T | snv | 1 | |||
rs137854465 | 0.925 | 0.160 | 15 | 48488230 | missense variant | A/G | snv | 1 | |||
rs137854478 | 0.851 | 0.160 | 15 | 48488233 | missense variant | C/T | snv | 1 | |||
rs137854472 | 0.925 | 0.160 | 15 | 48488448 | missense variant | T/C | snv | 8.0E-06 | 1 | ||
rs140593 | 0.925 | 0.160 | 15 | 48489896 | missense variant | C/G;T | snv | 1 | |||
rs140592 | 0.925 | 0.160 | 15 | 48489947 | missense variant | A/G | snv | 7.0E-06 | 1 | ||
rs137854477 | 0.925 | 0.160 | 15 | 48489979 | missense variant | C/T | snv | 1 | |||
rs137854463 | 1.000 | 0.160 | 15 | 48497391 | missense variant | T/G | snv | 1 | |||
rs140603 | 0.925 | 0.160 | 15 | 48503845 | stop gained | G/A;C;T | snv | 7.6E-04 | 1 | ||
rs137854462 | 1.000 | 0.160 | 15 | 48510115 | missense variant | T/A | snv | 1 | |||
rs137854480 | 0.742 | 0.200 | 15 | 48537629 | missense variant | G/A | snv | 2 | |||
rs363853 | 1.000 | 0.160 | 15 | 48596292 | missense variant | A/G | snv | 1 | |||
rs137854467 | 0.790 | 0.280 | 15 | 48600217 | missense variant | G/A | snv | 1 | |||
rs112660651 | 0.925 | 0.160 | 15 | 48610808 | missense variant | C/A;G;T | snv | 1 | |||
rs25403 | 0.882 | 0.200 | 15 | 48613073 | missense variant | G/A | snv | 1 |