Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913338 | 0.677 | 0.400 | 7 | 140753354 | missense variant | T/A;C;G | snv | 12 | |||
rs587782289 | 0.752 | 0.240 | 17 | 7674257 | missense variant | A/C;G;T | snv | 12 | |||
rs121913530 | 0.583 | 0.640 | 12 | 25245351 | missense variant | C/A;G;T | snv | 11 | |||
rs397516896 | 0.763 | 0.360 | 7 | 140753355 | missense variant | C/G;T | snv | 11 | |||
rs77375493 | 0.458 | 0.760 | 9 | 5073770 | missense variant | G/A;T | snv | 3.5E-04 | 10 | ||
rs121913351 | 0.776 | 0.240 | 7 | 140781611 | missense variant | C/A;G;T | snv | 4.0E-06 | 9 | ||
rs121913370 | 0.763 | 0.360 | 7 | 140753393 | missense variant | T/C;G | snv | 9 | |||
rs121913409 | 0.708 | 0.400 | 3 | 41224646 | missense variant | C/A;G;T | snv | 9 | |||
rs869025608 | 0.763 | 0.400 | 15 | 66435117 | missense variant | G/C;T | snv | 9 | |||
rs112445441 | 0.658 | 0.400 | 12 | 25245347 | missense variant | C/A;G;T | snv | 8 | |||
rs121913369 | 0.790 | 0.280 | 7 | 140753346 | missense variant | G/A;C | snv | 4.0E-06 | 8 | ||
rs121913240 | 0.672 | 0.440 | 12 | 25227342 | missense variant | T/A;C;G | snv | 6 | |||
rs121913378 | 0.776 | 0.280 | 7 | 140753337 | missense variant | C/A;G;T | snv | 6 | |||
rs121913386 | 0.807 | 0.120 | 9 | 21971018 | missense variant | G/A;T | snv | 6 | |||
rs727504317 | 0.807 | 0.320 | 15 | 66435145 | missense variant | G/A | snv | 6 | |||
rs121913535 | 0.742 | 0.320 | 12 | 25245348 | missense variant | C/A;G;T | snv | 5 | |||
rs121913246 | 0.827 | 0.200 | 7 | 116783360 | missense variant | A/G | snv | 4 | |||
rs121913428 | 0.827 | 0.120 | 7 | 55174015 | missense variant | G/A;C | snv | 4 | |||
rs113994088 | 0.925 | 0.080 | 2 | 29222584 | missense variant | C/G | snv | 3 | |||
rs121913238 | 0.732 | 0.240 | 12 | 25227343 | missense variant | G/C;T | snv | 3 | |||
rs121913444 | 0.724 | 0.160 | 7 | 55191831 | missense variant | T/A;C;G | snv | 3 | |||
rs121913465 | 0.763 | 0.160 | 7 | 55181312 | missense variant | G/T | snv | 3 | |||
rs149840192 | 0.807 | 0.080 | 7 | 55154129 | missense variant | C/A;T | snv | 3 | |||
rs28929495 | 0.807 | 0.120 | 7 | 55174014 | missense variant | G/A;C;T | snv | 3 | |||
rs662 | 0.485 | 0.840 | 7 | 95308134 | missense variant | T/C | snv | 0.38 | 0.42 | 3 |