Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs183334241 | 0.925 | 0.080 | 18 | 75288186 | missense variant | G/A;C | snv | 1.6E-04 | 2 | ||
rs78081605 | 0.925 | 0.080 | 18 | 75288051 | missense variant | G/C | snv | 8.0E-06 | 7.0E-06 | 2 | |
rs1188536960 | 0.882 | 0.120 | 15 | 45043305 | missense variant | A/G | snv | 5 | |||
rs11214077 | 0.752 | 0.120 | 11 | 112087953 | missense variant | A/G | snv | 6.6E-03 | 6.7E-03 | 12 | |
rs867966048 | 1.000 | 0.080 | 1 | 161340637 | missense variant | G/A;C | snv | 2 | |||
rs769177037 | 1.000 | 0.080 | 1 | 161328467 | missense variant | G/A;C;T | snv | 4.0E-06; 4.0E-06 | 1 | ||
rs770599902 | 1.000 | 0.080 | 1 | 161362382 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
rs33927012 | 1.000 | 0.080 | 1 | 17027802 | missense variant | A/G | snv | 1.2E-02 | 9.3E-03 | 1 | |
rs74799832 | 0.662 | 0.280 | 10 | 43121968 | missense variant | T/C | snv | 4.0E-06 | 33 | ||
rs79658334 | 0.662 | 0.360 | 10 | 43119548 | missense variant | G/A;C;T | snv | 1.2E-04; 4.3E-06 | 29 | ||
rs1799939 | 0.658 | 0.280 | 10 | 43114671 | missense variant | G/A;C;T | snv | 0.21 | 27 | ||
rs75076352 | 0.689 | 0.240 | 10 | 43114500 | missense variant | T/A;C;G | snv | 1.2E-05 | 24 | ||
rs77724903 | 0.672 | 0.280 | 10 | 43118460 | missense variant | A/G;T | snv | 4.0E-06; 2.1E-03 | 23 | ||
rs75996173 | 0.716 | 0.240 | 10 | 43114501 | missense variant | G/A;C;T | snv | 4.0E-06; 4.0E-06 | 21 | ||
rs76262710 | 0.724 | 0.280 | 10 | 43113648 | missense variant | T/A;C;G | snv | 4.0E-06; 4.0E-06 | 17 | ||
rs79781594 | 0.732 | 0.160 | 10 | 43113649 | missense variant | G/A;C;T | snv | 16 | |||
rs77939446 | 0.724 | 0.120 | 10 | 43113622 | missense variant | G/A;C;T | snv | 4.0E-06 | 15 | ||
rs75234356 | 0.716 | 0.240 | 10 | 43120144 | missense variant | T/G | snv | 1.2E-05 | 7.0E-06 | 14 | |
rs77709286 | 0.752 | 0.160 | 10 | 43114502 | missense variant | C/G | snv | 4.0E-06 | 12 | ||
rs78014899 | 0.742 | 0.160 | 10 | 43118392 | missense variant | G/A;C;T | snv | 8.0E-06 | 12 | ||
rs377767404 | 0.742 | 0.160 | 10 | 43114488 | missense variant | T/C | snv | 11 | |||
rs377767397 | 0.790 | 0.280 | 10 | 43113628 | missense variant | G/A;C;T | snv | 10 | |||
rs75873440 | 0.763 | 0.200 | 10 | 43112173 | missense variant | G/A;T | snv | 4.4E-05 | 10 | ||
rs77316810 | 0.776 | 0.200 | 10 | 43113654 | missense variant | T/A;C;G | snv | 10 | |||
rs377767406 | 0.776 | 0.120 | 10 | 43114491 | missense variant | G/A;T | snv | 4.0E-05; 4.0E-06 | 9 |