Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1256030 0.827 0.240 14 64280452 intron variant A/G;T snv 1
rs1256031 0.790 0.200 14 64279461 intron variant G/A;T snv 0.57 1