Source: GWASDB ×
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs28927680 | 11 | 116748357 | 3 prime UTR variant | C/G;T | snv | 4 | |||||
| rs2975634 | 7 | 30452077 | missense variant | C/A;T | snv | 4.0E-06; 6.3E-03 | 3 | ||||
| rs2980875 | 8 | 125469505 | intron variant | A/C;G;T | snv | 6 | |||||
| rs3093267 | 13 | 113118661 | missense variant | G/A;T | snv | 8.0E-05 | 6 | ||||
| rs33980385 | 19 | 40991388 | missense variant | A/G | snv | 6 | |||||
| rs3783567 | 2 | 112788378 | upstream gene variant | G/A;T | snv | 3 | |||||
| rs3890182 | 0.925 | 0.120 | 9 | 104885374 | intron variant | G/A;T | snv | 4 | |||
| rs473224 | 15 | 58445142 | intron variant | T/A;G | snv | 5 | |||||
| rs485538 | 15 | 58448978 | intron variant | C/G;T | snv | 5 | |||||
| rs485671 | 15 | 58448935 | intron variant | A/C;T | snv | 5 | |||||
| rs519113 | 1.000 | 0.080 | 19 | 44873027 | intron variant | C/G;T | snv | 6 | |||
| rs572410 | 15 | 58449185 | intron variant | C/G;T | snv | 4 | |||||
| rs588136 | 15 | 58438299 | intron variant | C/G;T | snv | 5 | |||||
| rs599839 | 0.724 | 0.360 | 1 | 109279544 | downstream gene variant | G/A;C | snv | 9 | |||
| rs673548 | 0.925 | 0.120 | 2 | 21014672 | intron variant | G/A;T | snv | 10 | |||
| rs676210 | 0.925 | 0.120 | 2 | 21008652 | missense variant | G/A;T | snv | 0.29 | 7 | ||
| rs711752 | 1.000 | 0.040 | 16 | 56962299 | splice region variant | G/A;C | snv | 6 | |||
| rs7241918 | 18 | 49634583 | intergenic variant | G/A;T | snv | 3 | |||||
| rs7499892 | 16 | 56972678 | intron variant | C/G;T | snv | 6 | |||||
| rs7518440 | 1 | 150818286 | non coding transcript exon variant | A/G;T | snv | 3 | |||||
| rs7666097 | 4 | 55124971 | intron variant | T/A;C | snv | 5 | |||||
| rs874565 | 18 | 49562320 | synonymous variant | C/A;T | snv | 9.4E-03 | 3 | ||||
| rs9341023 | 6 | 152062578 | intron variant | C/T | snv | 6 | |||||
| rs970548 | 10 | 45517829 | intron variant | A/C;T | snv | 3 | |||||
| rs35233375 | 12 | 120739357 | missense variant | G/A | snv | 7.0E-06 | 3 |