Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 | |
rs4680 | 0.442 | 0.920 | 22 | 19963748 | missense variant | G/A | snv | 0.46 | 0.44 | 249 | |
rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
rs746682028 | 0.645 | 0.480 | 11 | 27658414 | missense variant | C/A;T | snv | 4.0E-06; 4.0E-06 | 36 | ||
rs2254298 | 0.701 | 0.200 | 3 | 8760542 | intron variant | G/A | snv | 0.16 | 23 | ||
rs1176744 | 0.708 | 0.240 | 11 | 113932306 | missense variant | A/C | snv | 0.33 | 0.36 | 19 | |
rs10070190 | 0.925 | 0.040 | 5 | 26866262 | intergenic variant | G/A | snv | 0.60 | 2 | ||
rs11174202 | 0.925 | 0.040 | 12 | 61858476 | intron variant | A/G | snv | 0.49 | 2 | ||
rs11783752 | 0.925 | 0.040 | 8 | 20192013 | intergenic variant | G/A;C | snv | 2 | |||
rs12504244 | 0.925 | 0.040 | 4 | 54619021 | intergenic variant | C/A;G;T | snv | 2 | |||
rs2834070 | 0.925 | 0.040 | 21 | 33015144 | intron variant | G/T | snv | 0.24 | 2 | ||
rs4825476 | 0.925 | 0.040 | X | 123307628 | intron variant | G/A;C | snv | 2 | |||
rs75063949 | 0.925 | 0.040 | 6 | 25590813 | intron variant | C/G | snv | 0.14 | 2 |