Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13260300 1.000 0.080 8 74567389 regulatory region variant C/T snv 0.67 2
rs12988804
LRP2
1.000 0.080 2 169261301 intron variant C/T snv 0.24 2