Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 21
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 17
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 13
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 11
rs2896019
PNPLA3
0.790 0.160 22 43937814 intron variant T/G snv 0.20 8
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 7
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs2294915
PNPLA3
1.000 0.040 22 43945024 intron variant C/G;T snv 5
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs58542926
TM6SF2
0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 5
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 4
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 4
rs6982502 0.882 0.080 8 125467120 intron variant C/T snv 0.62 4
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 4
rs4823173
PNPLA3
0.827 0.200 22 43932850 intron variant G/A snv 0.24 0.18 4
rs2143571
SAMM50
0.827 0.080 22 43995806 intron variant G/A snv 0.25 4
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 3
rs206833 1.000 0.040 2 31485750 intergenic variant G/A snv 0.17 3
rs11976006
CREB5
1.000 0.040 7 28691895 intron variant G/A snv 6.1E-02 3
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 3