Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs7270101
ITPA
0.776 0.200 20 3213247 intron variant A/C snv 8.7E-02 9.7E-02 10
rs72613567
HSD17B13
0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs7254880
ZNF699
0.882 0.160 19 9298599 intron variant C/G snv 0.16 4
rs7158733
ATXN3
1.000 0.080 14 92070879 stop gained G/A;T snv 1.2E-05; 0.27 1
rs7080536
HABP2 ; NRAP
0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 27
rs705382
PON1
0.827 0.200 7 95325909 upstream gene variant C/G snv 0.53 5
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs6897932
IL7R
0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs6834059
AFP
0.925 0.080 4 73435958 intron variant C/G snv 0.23 2
rs675520
LOC102723649 ; LOC105378018
0.925 0.080 6 137672095 non coding transcript exon variant A/G;T snv 2
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs6715787
EPAS1
0.851 0.200 2 46349033 intron variant C/G;T snv 4
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs6591182
EHBP1L1
0.925 0.080 11 65582285 missense variant T/G snv 0.47 0.45 2
rs6487679 0.925 0.080 12 9218736 intergenic variant C/T snv 0.80 2
rs643608 0.925 0.080 21 43348682 intergenic variant C/T snv 0.69 2
rs642588
IGF2R
0.925 0.120 6 159990235 intron variant A/G snv 0.83 2
rs641738
LOC112268246 ; TMC4 ; MBOAT7
0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs629849
IGF2R
0.827 0.160 6 160073377 missense variant A/C;G;T snv 0.90 0.91 9
rs61330082
NAMPT
0.732 0.320 7 106286419 upstream gene variant G/A snv 0.22 13
rs5998152
DEPDC5
0.827 0.160 22 31867176 intron variant T/C snv 0.37 5