Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs641738
LOC112268246 ; TMC4 ; MBOAT7
0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs13361189 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 13
rs1010023
PNPLA3
0.851 0.080 22 43940218 intron variant T/C snv 0.20 4
rs3213445
CHKB-CPT1B ; CPT1B
0.851 0.120 22 50577409 missense variant T/C snv 0.12 8.9E-02 4
rs2862954
ERLIN1
0.925 0.040 10 100152307 missense variant T/C snv 0.34 0.32 2
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60