Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7972947 | 1.000 | 0.040 | 12 | 2061267 | intron variant | C/A;T | snv | 1 | |||
rs2007044 | 0.882 | 0.040 | 12 | 2235794 | intron variant | A/G | snv | 0.50 | 1 | ||
rs1006737 | 0.695 | 0.120 | 12 | 2236129 | intron variant | G/A | snv | 0.36 | 6 | ||
rs2159100 | 0.925 | 0.040 | 12 | 2237227 | intron variant | C/A;G;T | snv | 1 | |||
rs4765905 | 0.827 | 0.040 | 12 | 2240418 | intron variant | G/A;C | snv | 2 | |||
rs10774037 | 0.882 | 0.040 | 12 | 2311360 | intron variant | G/A | snv | 0.77 | 2 | ||
rs2239063 | 1.000 | 0.040 | 12 | 2402665 | intron variant | A/C | snv | 0.23 | 1 |