Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs61755783
PRPH2
0.763 0.080 6 42721911 missense variant G/A snv 1.4E-05 11
rs61755792
PRPH2
0.763 0.160 6 42721821 missense variant G/A;C snv 10
rs1555968874
CHM
0.925 0.040 X 86027530 inframe deletion AGC/- delins 2