Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10927887 | 0.925 | 0.040 | 1 | 16024780 | missense variant | A/C;G | snv | 0.55 | 3 | ||
rs3798220 | 0.732 | 0.160 | 6 | 160540105 | missense variant | T/C | snv | 5.6E-02 | 3.1E-02 | 16 | |
rs10455872 | 0.662 | 0.320 | 6 | 160589086 | intron variant | A/G | snv | 4.3E-02 | 33 | ||
rs12567209 | 0.807 | 0.080 | 1 | 162066689 | upstream gene variant | G/A | snv | 8.6E-02 | 6 | ||
rs4819554 | 0.776 | 0.320 | 22 | 17084145 | upstream gene variant | G/A | snv | 0.84 | 10 | ||
rs5219 | 0.701 | 0.360 | 11 | 17388025 | stop gained | T/A;C | snv | 0.64 | 25 | ||
rs141322087 | 0.851 | 0.160 | 11 | 17404552 | missense variant | C/T | snv | 1.2E-05 | 2.1E-05 | 13 | |
rs1344172059 | 0.882 | 0.080 | 11 | 17430838 | missense variant | C/T | snv | 7.0E-06 | 12 | ||
rs2241562 | 0.925 | 0.040 | 5 | 175684809 | intron variant | G/C;T | snv | 1.0E-03 | 2 | ||
rs766265889 | 0.827 | 0.240 | 2 | 178535508 | stop gained | G/A;T | snv | 8.0E-06; 4.0E-06 | 11 | ||
rs548787835 | 1.000 | 0.040 | 5 | 179823911 | missense variant | C/G;T | snv | 1.2E-05; 1.6E-05 | 1 | ||
rs12564445 | 0.851 | 0.040 | 1 | 201376359 | intron variant | G/A | snv | 0.27 | 5 | ||
rs7311358 | 0.827 | 0.160 | 12 | 20862826 | missense variant | G/A | snv | 0.81 | 0.72 | 6 | |
rs1595065 | 0.925 | 0.040 | 2 | 211377916 | 3 prime UTR variant | G/A | snv | 0.73 | 2 | ||
rs1595064 | 0.925 | 0.040 | 2 | 211378020 | 3 prime UTR variant | G/A;C | snv | 2 | |||
rs13003941 | 0.925 | 0.040 | 2 | 211378978 | 3 prime UTR variant | G/C;T | snv | 0.26 | 2 | ||
rs10932374 | 0.925 | 0.040 | 2 | 211379678 | 3 prime UTR variant | G/A | snv | 0.23 | 2 | ||
rs3748960 | 0.925 | 0.040 | 2 | 211383109 | 3 prime UTR variant | C/T | snv | 0.96 | 2 | ||
rs4149056 | 0.633 | 0.480 | 12 | 21178615 | missense variant | T/C | snv | 0.13 | 0.12 | 45 | |
rs267607499 | 0.851 | 0.160 | 2 | 219418809 | missense variant | A/G;T | snv | 4 | |||
rs10757274 | 0.701 | 0.320 | 9 | 22096056 | intron variant | A/G | snv | 0.41 | 22 | ||
rs2383206 | 0.742 | 0.320 | 9 | 22115027 | intron variant | A/G | snv | 0.49 | 17 | ||
rs2383207 | 0.695 | 0.280 | 9 | 22115960 | intron variant | A/G | snv | 0.64 | 22 | ||
rs10757278 | 0.620 | 0.520 | 9 | 22124478 | intron variant | A/G | snv | 0.40 | 44 | ||
rs699 | 0.501 | 0.800 | 1 | 230710048 | missense variant | A/G | snv | 0.55 | 0.58 | 134 |