Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2023239
CNR1
0.724 0.160 6 88150763 intron variant T/C snv 0.21 20
rs4917
AHSG
0.790 0.160 3 186619924 missense variant T/C snv 0.68 0.68 9
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 7
rs10822184
REEP3
1.000 10 63577393 intron variant T/C;G snv 2