Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1057520039 | 0.882 | 0.200 | 19 | 1207169 | stop gained | C/G;T | snv | 4 | |||
| rs730881976 | 0.882 | 0.240 | 19 | 1220702 | stop gained | C/A;G | snv | 4 | |||
| rs1085307466 | 1.000 | 0.160 | 19 | 1221990 | stop gained | C/T | snv | 3 | |||
| rs121913324 | 1.000 | 0.160 | 19 | 1207022 | stop gained | C/T | snv | 3 | |||
| rs1131690940 | 1.000 | 0.160 | 19 | 1220641 | stop gained | C/T | snv | 2 | |||
| rs137853076 | 1.000 | 0.160 | 19 | 1207163 | stop gained | A/G;T | snv | 4.1E-06 | 2 | ||
| rs778376925 | 1.000 | 0.160 | 19 | 1207093 | stop gained | C/A;G;T | snv | 1.2E-05 | 2 | ||
| rs864622488 | 1.000 | 0.160 | 19 | 1222987 | stop gained | G/A;T | snv | 2 | |||
| rs137853075 | 1.000 | 0.160 | 19 | 1221237 | stop gained | C/A;T | snv | 1 | |||
| rs137853082 | 1.000 | 0.160 | 19 | 1220700 | stop gained | G/A;C | snv | 1 | |||
| rs137853083 | 1.000 | 0.160 | 19 | 1221216 | stop gained | C/G;T | snv | 4.0E-06 | 1 | ||
| rs137854584 | 1.000 | 0.160 | 19 | 1207082 | stop gained | G/T | snv | 1 | |||
| rs786201213 | 1.000 | 0.160 | 19 | 1220613 | stop gained | C/A;T | snv | 1 | |||
| rs786201349 | 1.000 | 0.160 | 19 | 1220376 | stop gained | C/G;T | snv | 1 | |||
| rs121913315 | 0.882 | 0.160 | 19 | 1220488 | missense variant | G/A;T | snv | 5 | |||
| rs1057520038 | 0.925 | 0.160 | 19 | 1220627 | missense variant | G/A | snv | 2 | |||
| rs137853077 | 1.000 | 0.160 | 19 | 1207113 | missense variant | T/C | snv | 2 | |||
| rs730881979 | 1.000 | 0.160 | 19 | 1220434 | missense variant | G/A | snv | 2 | |||
| rs878853247 | 1.000 | 0.160 | 19 | 1220692 | missense variant | G/C;T | snv | 2 | |||
| rs886037859 | 1.000 | 0.160 | 19 | 1220450 | missense variant | A/G | snv | 2 | |||
| rs1057520040 | 1.000 | 0.160 | 19 | 1218449 | missense variant | A/G | snv | 1 | |||
| rs1057520041 | 1.000 | 0.160 | 19 | 1220438 | missense variant | T/A | snv | 1 | |||
| rs1057520042 | 1.000 | 0.160 | 19 | 1222988 | missense variant | G/C | snv | 1 | |||
| rs1060499958 | 1.000 | 0.160 | 19 | 1219356 | missense variant | T/C | snv | 1 | |||
| rs1568708382 | 1.000 | 0.160 | 19 | 1220708 | missense variant | G/A | snv | 1 |