Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs58542926
TM6SF2
0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs1800730
HFE ; LOC108783645
0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs28934571
TP53
0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 15
rs72613567
HSD17B13
0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs11127
GNLY
0.925 0.160 2 85697606 missense variant C/T snv 0.39 0.31 3
rs2148356 1.000 0.080 9 7395038 intergenic variant G/A;C snv 2
rs1866139
GNLY
1.000 0.080 2 85694266 intron variant G/C snv 0.51 2
rs7959378
TFCP2
1.000 0.080 12 51173447 upstream gene variant A/C snv 0.41 2