Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3745567
C3
19 6690760 intron variant C/T snv 0.11 0.11 1
rs3753394
CFH
0.882 0.040 1 196651787 upstream gene variant C/T snv 0.22 1