Source: UNIPROT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs193922525 | 1.000 | 0.120 | 7 | 117664770 | missense variant | G/A | snv | 1 | |||
| rs200553511 | 1.000 | 0.120 | 7 | 117610614 | missense variant | G/A;T | snv | 4.0E-06 | 1 | ||
| rs201958172 | 1.000 | 0.120 | 7 | 117530983 | missense variant | G/A;C;T | snv | 1.4E-04; 4.0E-06 | 1 | ||
| rs201978662 | 1.000 | 0.120 | 7 | 117592004 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
| rs397508146 | 1.000 | 0.120 | 7 | 117540267 | missense variant | T/C | snv | 1 | |||
| rs397508195 | 1.000 | 0.120 | 7 | 117548797 | missense variant | G/C;T | snv | 1 | |||
| rs397508223 | 1.000 | 0.120 | 7 | 117559581 | stop gained | G/C;T | snv | 1 | |||
| rs397508267 | 1.000 | 0.120 | 7 | 117590353 | missense variant | A/C | snv | 4.0E-06 | 1 | ||
| rs397508272 | 1.000 | 0.120 | 7 | 117509038 | missense variant | T/C;G | snv | 1 | |||
| rs397508277 | 1.000 | 0.120 | 7 | 117590379 | missense variant | A/G | snv | 1 | |||
| rs397508280 | 1.000 | 0.120 | 7 | 117590385 | missense variant | T/C | snv | 1 | |||
| rs397508282 | 1.000 | 0.120 | 7 | 117590387 | missense variant | G/A | snv | 1 | |||
| rs397508306 | 1.000 | 0.120 | 7 | 117591968 | missense variant | A/G;T | snv | 4.3E-06; 4.3E-06 | 1 | ||
| rs397508311 | 1.000 | 0.120 | 7 | 117591996 | missense variant | T/C | snv | 1 | |||
| rs397508313 | 1.000 | 0.120 | 7 | 117592023 | missense variant | T/C | snv | 1 | |||
| rs397508314 | 1.000 | 0.120 | 7 | 117592026 | missense variant | A/C;G;T | snv | 8.6E-06; 4.3E-06 | 1 | ||
| rs397508315 | 1.000 | 0.120 | 7 | 117592027 | missense variant | T/G | snv | 1 | |||
| rs397508316 | 1.000 | 0.120 | 7 | 117592049 | missense variant | G/A;C | snv | 4.1E-06 | 1 | ||
| rs397508318 | 1.000 | 0.120 | 7 | 117592065 | missense variant | T/C | snv | 1 | |||
| rs397508403 | 1.000 | 0.120 | 7 | 117509128 | missense variant | T/A;C | snv | 1 | |||
| rs397508428 | 1.000 | 0.120 | 7 | 117603624 | missense variant | A/G | snv | 1 | |||
| rs397508479 | 1.000 | 0.120 | 7 | 117610544 | missense variant | T/G | snv | 4.0E-06 | 1 | ||
| rs397508531 | 1.000 | 0.120 | 7 | 117611733 | missense variant | T/C | snv | 1 | |||
| rs397508553 | 1.000 | 0.120 | 7 | 117614654 | missense variant | A/G | snv | 3.6E-05 | 4.9E-05 | 1 | |
| rs397508616 | 1.000 | 0.120 | 7 | 117642564 | missense variant | T/C;G | snv | 1 |