Source: UNIPROT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs397508267 | 1.000 | 0.120 | 7 | 117590353 | missense variant | A/C | snv | 4.0E-06 | 1 | ||
rs121909037 | 1.000 | 0.120 | 7 | 117611653 | missense variant | A/C;G | snv | 4.0E-06 | 1 | ||
rs397508288 | 0.882 | 0.200 | 7 | 117590409 | missense variant | A/C;G | snv | 4.0E-06 | 1 | ||
rs397508464 | 0.851 | 0.160 | 7 | 117530918 | missense variant | A/C;G | snv | 8.0E-06 | 1 | ||
rs79635528 | 1.000 | 0.120 | 7 | 117611695 | missense variant | A/C;G | snv | 4.0E-06 | 1 | ||
rs397508314 | 1.000 | 0.120 | 7 | 117592026 | missense variant | A/C;G;T | snv | 8.6E-06; 4.3E-06 | 1 | ||
rs76371115 | 0.807 | 0.160 | 7 | 117531041 | missense variant | A/C;G;T | snv | 8.0E-06 | 1 | ||
rs121909042 | 1.000 | 0.120 | 7 | 117652875 | missense variant | A/C;T | snv | 4.0E-06 | 1 | ||
rs121909008 | 0.925 | 0.160 | 7 | 117603612 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 1 | |
rs121909031 | 1.000 | 0.120 | 7 | 117530951 | missense variant | A/G | snv | 1 | |||
rs150691494 | 1.000 | 0.120 | 7 | 117540132 | missense variant | A/G | snv | 2.9E-04 | 1.8E-04 | 1 | |
rs1800103 | 0.925 | 0.160 | 7 | 117592588 | missense variant | A/G | snv | 7.7E-04 | 4.4E-04 | 1 | |
rs191456345 | 0.925 | 0.160 | 7 | 117536576 | missense variant | A/G | snv | 1.8E-04 | 1.1E-04 | 1 | |
rs201124247 | 0.882 | 0.160 | 7 | 117592008 | missense variant | A/G | snv | 3.1E-05 | 1 | ||
rs397508225 | 0.925 | 0.160 | 7 | 117559609 | missense variant | A/G | snv | 4.0E-06 | 1 | ||
rs397508277 | 1.000 | 0.120 | 7 | 117590379 | missense variant | A/G | snv | 1 | |||
rs397508428 | 1.000 | 0.120 | 7 | 117603624 | missense variant | A/G | snv | 1 | |||
rs397508553 | 1.000 | 0.120 | 7 | 117614654 | missense variant | A/G | snv | 3.6E-05 | 4.9E-05 | 1 | |
rs397508621 | 1.000 | 0.120 | 7 | 117642592 | missense variant | A/G | snv | 4.0E-06 | 1 | ||
rs75389940 | 0.882 | 0.120 | 7 | 117627753 | missense variant | A/G | snv | 4.0E-06 | 1 | ||
rs1800074 | 1.000 | 0.120 | 7 | 117504330 | missense variant | A/G;T | snv | 4.0E-06 | 1 | ||
rs397508306 | 1.000 | 0.120 | 7 | 117591968 | missense variant | A/G;T | snv | 4.3E-06; 4.3E-06 | 1 | ||
rs1177201180 | 1.000 | 0.120 | 7 | 117592160 | missense variant | A/T | snv | 1 | |||
rs121909033 | 1.000 | 0.120 | 7 | 117592110 | missense variant | A/T | snv | 1 | |||
rs397508804 | 1.000 | 0.120 | 7 | 117536663 | missense variant | A/T | snv | 1.2E-05 | 1 |