Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs779724499 | 12 | 54411885 | missense variant | G/A | snv | 1 | |||||
rs7795743 | 7 | 55182437 | non coding transcript exon variant | G/A | snv | 0.56 | 1 | ||||
rs77709286 | 0.752 | 0.160 | 10 | 43114502 | missense variant | C/G | snv | 4.0E-06 | 12 | ||
rs776880789 | 0.925 | 0.080 | 11 | 101128241 | missense variant | G/C;T | snv | 4.7E-06; 4.7E-06 | 4 | ||
rs7758229 | 0.732 | 0.120 | 6 | 160419220 | intron variant | G/A;T | snv | 16 | |||
rs773895706 | 0.925 | 0.080 | 15 | 79090236 | missense variant | G/A | snv | 4.2E-06 | 3 | ||
rs77375493 | 0.458 | 0.760 | 9 | 5073770 | missense variant | G/A;T | snv | 3.5E-04 | 187 | ||
rs772893086 | 0.925 | 0.080 | 21 | 45176099 | missense variant | A/C;G;T | snv | 4.0E-06 | 4 | ||
rs772551056 | 0.807 | 0.120 | 1 | 17044824 | missense variant | C/A;T | snv | 4.0E-06 | 9 | ||
rs77191406 | 0.790 | 0.280 | 6 | 137881704 | 3 prime UTR variant | C/T | snv | 7.2E-04 | 12 | ||
rs771386507 | 0.882 | 0.120 | 6 | 31355479 | missense variant | C/T | snv | 4.0E-06 | 6 | ||
rs771308693 | 8 | 140752306 | missense variant | G/A | snv | 3.2E-05 | 7.0E-06 | 2 | |||
rs769483475 | 0.925 | 0.080 | 11 | 35229231 | missense variant | G/A | snv | 8.0E-06 | 3 | ||
rs768949233 | 0.851 | 0.040 | 2 | 9490466 | missense variant | G/C;T | snv | 4.0E-06 | 5 | ||
rs768827923 | 0.851 | 0.080 | 1 | 9721816 | missense variant | T/G | snv | 6 | |||
rs767649 | 0.695 | 0.480 | 21 | 25572410 | intron variant | T/A | snv | 7.5E-02 | 18 | ||
rs767151455 | 0.925 | 0.080 | 17 | 39708379 | missense variant | C/T | snv | 8.0E-06 | 4 | ||
rs766914563 | 0.732 | 0.320 | 2 | 136115082 | synonymous variant | C/T | snv | 7.0E-06 | 16 | ||
rs7668666 | 1.000 | 4 | 186080138 | intron variant | C/A;T | snv | 4 | ||||
rs765431049 | 0.925 | 0.040 | 7 | 93890271 | missense variant | C/T | snv | 1.6E-05 | 4 | ||
rs7646409 | 0.882 | 0.040 | 3 | 179182405 | intron variant | T/C | snv | 0.26 | 4 | ||
rs76322625 | 1.000 | 0.080 | 7 | 116798111 | 3 prime UTR variant | C/A;T | snv | 3 | |||
rs763059810 | 0.623 | 0.600 | 2 | 136115750 | missense variant | T/C | snv | 4.0E-06 | 41 | ||
rs762846821 | 0.614 | 0.320 | 17 | 7675151 | missense variant | C/A;T | snv | 8.0E-06 | 57 | ||
rs76262710 | 0.724 | 0.280 | 10 | 43113648 | missense variant | T/A;C;G | snv | 4.0E-06; 4.0E-06 | 17 |