| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs73071328 | 1.000 | 0.160 | 3 | 41768563 | intron variant | A/C | snv | 0.12 | 1 | ||
| rs73073342 | 1.000 | 0.160 | 3 | 41797963 | intron variant | A/C | snv | 0.12 | 1 | ||
| rs73079307 | 1.000 | 0.160 | 3 | 41820781 | intron variant | A/C | snv | 0.12 | 1 | ||
| rs75341503 | 1.000 | 0.160 | 7 | 21897080 | intron variant | A/C | snv | 0.26 | 1 | ||
| rs77778906 | 1.000 | 0.160 | 3 | 41904120 | intron variant | A/C | snv | 0.12 | 1 | ||
| rs1801274 | 0.597 | 0.800 | 1 | 161509955 | missense variant | A/C;G | snv | 4.0E-06; 0.48 | 46 | ||
| rs78311289 | 0.689 | 0.440 | 4 | 1806162 | missense variant | A/C;G | snv | 4.0E-06 | 25 | ||
| rs2228055 | 0.851 | 0.280 | 11 | 117994131 | missense variant | A/C;G | snv | 8.2E-02 | 4 | ||
| rs6768972 | 1.000 | 0.160 | 3 | 3180101 | upstream gene variant | A/C;G | snv | 2 | |||
| rs10212536 | 1.000 | 0.160 | 3 | 41785534 | intron variant | A/C;G | snv | 1 | |||
| rs10452020 | 1.000 | 0.160 | 3 | 41774459 | intron variant | A/C;G | snv | 1 | |||
| rs12185908 | 1.000 | 0.160 | 3 | 41793000 | intron variant | A/C;G | snv | 1 | |||
| rs17284313 | 1.000 | 0.160 | 3 | 41945295 | intron variant | A/C;G | snv | 1 | |||
| rs73830516 | 1.000 | 0.160 | 3 | 41834564 | intron variant | A/C;G | snv | 1 | |||
| rs7649989 | 1.000 | 0.160 | 3 | 41824351 | intron variant | A/C;G | snv | 1 | |||
| rs80066790 | 1.000 | 0.160 | 3 | 41959351 | intron variant | A/C;G | snv | 1 | |||
| rs9847975 | 1.000 | 0.160 | 3 | 41745412 | intron variant | A/C;G | snv | 1 | |||
| rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 | ||
| rs2228570 | 0.521 | 0.760 | 12 | 47879112 | start lost | A/C;G;T | snv | 0.63 | 99 | ||
| rs760043106 | 0.645 | 0.440 | 17 | 7674947 | missense variant | A/C;G;T | snv | 32 | |||
| rs1057519981 | 0.689 | 0.440 | 17 | 7674251 | missense variant | A/C;G;T | snv | 22 | |||
| rs876660333 | 0.742 | 0.360 | 17 | 7673805 | missense variant | A/C;G;T | snv | 13 | |||
| rs1057519978 | 0.763 | 0.360 | 17 | 7675191 | missense variant | A/C;G;T | snv | 12 | |||
| rs121918465 | 0.827 | 0.200 | 12 | 112450407 | missense variant | A/C;G;T | snv | 7 | |||
| rs3134603 | 0.851 | 0.360 | 6 | 32158225 | non coding transcript exon variant | A/C;G;T | snv | 4 |