Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1169288 | 0.776 | 0.160 | 12 | 120978847 | missense variant | A/C;T | snv | 0.35 | 6 | ||
rs2244608 | 0.882 | 0.160 | 12 | 120979185 | intron variant | A/G | snv | 0.29 | 4 | ||
rs2259816 | 0.827 | 0.280 | 12 | 120997784 | synonymous variant | G/A;T | snv | 6.7E-06; 0.40 | 3 | ||
rs2393791 | 0.925 | 0.160 | 12 | 120986153 | intron variant | C/T | snv | 0.62 | 3 | ||
rs7310409 | 0.925 | 0.160 | 12 | 120987058 | intron variant | A/C;G;T | snv | 3 | |||
rs1169310 | 12 | 121001630 | 3 prime UTR variant | G/A | snv | 0.31 | 2 | ||||
rs1183910 | 1.000 | 0.080 | 12 | 120983004 | intron variant | G/A | snv | 0.28 | 2 | ||
rs12427353 | 1.000 | 0.080 | 12 | 120989098 | intron variant | G/A;C;T | snv | 2 | |||
rs2464196 | 0.742 | 0.320 | 12 | 120997624 | missense variant | G/A | snv | 0.34 | 0.27 | 2 | |
rs1169306 | 12 | 121000508 | 3 prime UTR variant | C/T | snv | 0.31 | 1 | ||||
rs11065385 | 12 | 120985583 | intron variant | A/G | snv | 0.72 | 1 | ||||
rs1169286 | 1.000 | 0.080 | 12 | 120981253 | intron variant | T/C | snv | 0.39 | 1 | ||
rs1169300 | 0.882 | 0.080 | 12 | 120993422 | intron variant | G/A | snv | 0.27 | 1 | ||
rs1169303 | 12 | 120998573 | intron variant | A/C;G | snv | 0.45 | 1 | ||||
rs2259820 | 0.882 | 0.160 | 12 | 120997539 | synonymous variant | C/T | snv | 0.34 | 0.26 | 1 | |
rs2393775 | 12 | 120986771 | intron variant | G/A;C | snv | 1 | |||||
rs2464195 | 12 | 120997672 | missense variant | G/A | snv | 0.39 | 0.31 | 1 | |||
rs7979473 | 12 | 120982457 | intron variant | A/C;G | snv | 1 | |||||
rs7979478 | 12 | 120982460 | intron variant | A/C;G;T | snv | 1 | |||||
rs735396 | 12 | 121001041 | 3 prime UTR variant | T/C | snv | 0.39 | 0.31 | 1 |