Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1744297
ASPG
14 104102135 intron variant T/C snv 0.86 12
rs2238732
PRODH
22 18927834 intron variant C/G;T snv 7
rs12613336 2 210704675 regulatory region variant T/C snv 0.19 6
rs13244654
SUMF2
7 56079263 intron variant T/C snv 0.48 4
rs62149891
CCT4
2 61877999 intron variant A/G snv 1.0E-01 3