Source: GWASDB
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3828309 | 0.882 | 0.160 | 2 | 233271764 | intron variant | A/G | snv | 0.42 | 3 | ||
| rs10210302 | 1.000 | 0.040 | 2 | 233250193 | intron variant | C/A;T | snv | 1 | |||
| rs12994997 | 1.000 | 0.040 | 2 | 233264857 | intron variant | G/A;C | snv | 0.45; 4.0E-06 | 1 | ||
| rs2241880 | 0.627 | 0.600 | 2 | 233274722 | missense variant | A/G | snv | 0.45 | 0.44 | 1 | |
| rs3792109 | 1.000 | 0.040 | 2 | 233275771 | non coding transcript exon variant | G/A | snv | 0.45 | 0.42 | 1 |