Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1801270 | 0.689 | 0.400 | 6 | 36684194 | missense variant | C/A;T | snv | 0.15; 4.4E-05 | 22 | ||
rs11540652 | 0.592 | 0.640 | 17 | 7674220 | missense variant | C/A;G;T | snv | 1.2E-05 | 20 | ||
rs937283 | 0.716 | 0.200 | 12 | 68808384 | 5 prime UTR variant | A/G | snv | 0.37 | 19 | ||
rs371769427 | 0.683 | 0.400 | 21 | 43104346 | missense variant | G/A;T | snv | 8.0E-06 | 17 | ||
rs735482 | 0.742 | 0.160 | 19 | 45408744 | missense variant | A/C | snv | 0.21 | 0.20 | 16 | |
rs1046282 | 0.776 | 0.160 | 19 | 45407414 | 3 prime UTR variant | A/G | snv | 0.30 | 10 | ||
rs121917887 | 0.790 | 0.120 | 17 | 51161744 | missense variant | A/G | snv | 6.0E-05 | 7.0E-05 | 10 | |
rs3212948 | 0.776 | 0.160 | 19 | 45421104 | intron variant | G/C | snv | 0.53 | 10 | ||
rs4769793 | 0.807 | 0.120 | 13 | 29985289 | intergenic variant | G/C | snv | 8 | |||
rs12918952 | 0.851 | 0.120 | 16 | 78386878 | missense variant | G/A;C;T | snv | 7 | |||
rs738791 | 0.851 | 0.120 | 22 | 23775338 | intron variant | C/T | snv | 0.37 | 6 | ||
rs78768932 | 0.882 | 0.080 | 12 | 120222977 | missense variant | C/G;T | snv | 5.4E-03 | 5.4E-03 | 6 | |
rs1329032366 | 0.882 | 0.080 | 4 | 94654530 | missense variant | A/G | snv | 4.0E-06 | 5 | ||
rs374733251 | 0.882 | 0.080 | 7 | 116740993 | missense variant | A/G | snv | 6.0E-05 | 7.7E-05 | 5 | |
rs377444977 | 0.882 | 0.080 | 7 | 55143443 | missense variant | G/A | snv | 5.2E-05 | 2.1E-05 | 5 |