Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs57968458 0.882 0.160 17 16916785 intergenic variant G/A snv 0.15 3
rs57104699
DNAH11
0.882 0.160 7 21888461 intron variant C/A snv 0.26 3
rs56219066
ELL2
0.882 0.160 5 95907227 intron variant T/A;C snv 3
rs138740
TOM1
0.882 0.160 22 35303589 intron variant C/T snv 0.51 3
rs73071352
ULK4
0.882 0.160 3 41786808 intron variant A/G snv 0.12 3
rs9848754
ULK4
0.882 0.160 3 41712155 intron variant C/T snv 0.18 3
rs6919908
USP8P1 ; HLA-B
0.882 0.160 6 31277183 non coding transcript exon variant T/C snv 0.83 3
rs74998556
TNFRSF13B
0.925 0.080 17 16936468 intron variant A/T snv 0.16 2