Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs16847548 | 0.807 | 0.120 | 1 | 162065484 | upstream gene variant | T/C | snv | 0.22 | 8 | ||
rs4657139 | 0.925 | 0.120 | 1 | 162060117 | intergenic variant | A/T | snv | 0.48 | 3 | ||
rs146695489 | 0.925 | 0.160 | 11 | 17470170 | missense variant | T/C | snv | 2.5E-04 | 5.6E-05 | 2 | |
rs1563145763 | 1.000 | 0.120 | 7 | 92099838 | stop gained | G/A | snv | 1 | |||
rs796052199 | 1.000 | 0.120 | 7 | 92002212 | missense variant | T/A | snv | 1 | |||
rs796052200 | 1.000 | 0.120 | 7 | 92045186 | missense variant | T/A | snv | 4.0E-06 | 1 | ||
rs1408198357 | 1.000 | 0.120 | 4 | 113373391 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 1 | |
rs755287627 | 1.000 | 0.120 | 4 | 113353494 | missense variant | A/G | snv | 4.0E-06 | 1 | ||
rs796052197 | 1.000 | 0.120 | 4 | 113354767 | missense variant | T/C | snv | 1 | |||
rs796052198 | 1.000 | 0.120 | 4 | 113356741 | missense variant | T/C | snv | 1 | |||
rs1047624774 | 1.000 | 0.120 | 1 | 203700807 | missense variant | T/C | snv | 4.0E-06 | 3.5E-05 | 2 | |
rs786205745 | 0.807 | 0.320 | 12 | 2504538 | missense variant | G/A;C | snv | 6 | |||
rs79891110 | 0.807 | 0.320 | 12 | 2504944 | stop gained | G/A;T | snv | 6 | |||
rs587782933 | 0.827 | 0.200 | 12 | 2504526 | missense variant | G/A | snv | 5 | |||
rs750835733 | 1.000 | 0.120 | 12 | 2593252 | missense variant | C/G;T | snv | 4.0E-06 | 1 | ||
rs786205748 | 1.000 | 0.120 | 12 | 2566465 | missense variant | C/T | snv | 1 | |||
rs1343191564 | 1.000 | 0.120 | 12 | 2688616 | missense variant | G/A | snv | 1 | |||
rs377564636 | 1.000 | 0.120 | 12 | 2679529 | missense variant | G/A | snv | 4.1E-06 | 1 | ||
rs749945590 | 1.000 | 0.120 | 12 | 2688601 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 | 1 | |
rs267607277 | 0.807 | 0.120 | 14 | 90404386 | missense variant | A/G | snv | 6 | |||
rs730882252 | 0.882 | 0.120 | 14 | 90404482 | missense variant | A/G | snv | 3 | |||
rs199744595 | 0.925 | 0.120 | 14 | 90404693 | missense variant | C/G;T | snv | 2.4E-05 | 2 | ||
rs1085307479 | 1.000 | 0.120 | 14 | 90404691 | missense variant | T/C | snv | 1 | |||
rs398124647 | 0.807 | 0.120 | 2 | 47161851 | missense variant | T/A;C | snv | 6 | |||
rs11551462 | 0.925 | 0.120 | 2 | 47160802 | missense variant | A/G | snv | 2 |