Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs670139
MS4A4A ; MS4A4E
0.925 0.080 11 60204322 intron variant G/A;T snv 1
rs6052751
RPS4XP2
20 4664427 intron variant G/A;C snv 1
rs2756271
RPS4XP2 ; PRNP
20 4684616 intron variant A/G;T snv 1