Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs58542926
TM6SF2
0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs641738
LOC112268246 ; TMC4 ; MBOAT7
0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs2228603
NCAN
0.790 0.360 19 19219115 missense variant C/A;T snv 2.8E-05; 5.9E-02 12
rs626283
TMC4 ; MBOAT7 ; LOC112268246
0.827 0.160 19 54173307 upstream gene variant C/G snv 0.61 7
rs4074
CXCL1
0.827 0.200 4 73870427 intron variant A/G snv 0.46 6
rs10392
PPP1R16B
0.882 0.160 20 38922292 3 prime UTR variant G/A snv 0.17 6
rs441
ALDH2
0.882 0.200 12 111791045 intron variant T/C snv 0.18 4
rs2303015
CALCOCO2
0.851 0.160 17 48852546 missense variant T/C snv 7.4E-02 0.12 4
rs752949
SLC1A2
0.925 0.160 11 35306201 synonymous variant C/T snv 0.23 0.22 3