Source: GWASDB ×
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 25
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 11
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 10
rs2126259
LOC157273
1.000 8 9327636 intron variant T/C snv 0.87 7
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 6
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 5
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 4
rs2071303
LOC108783645 ; HFE
0.882 0.120 6 26091108 splice region variant T/C snv 0.38 0.36 3
rs1461729
LOC157273
1.000 8 9329732 intron variant A/G snv 0.88 3
rs2281135
PNPLA3
0.851 0.160 22 43936690 intron variant G/A snv 0.19 3
rs2896019
PNPLA3
0.790 0.160 22 43937814 intron variant T/G snv 0.20 3
rs12447924
CETP
1.000 16 56960280 upstream gene variant C/T snv 0.76 2
rs12597002
CETP
1.000 16 56968492 intron variant C/A snv 0.25 2
rs1572982
HFE
0.827 0.200 6 26094139 intron variant G/A;T snv 0.52; 8.0E-06 2
rs6601299
LOC157273
0.925 0.040 8 9327181 intron variant T/C snv 0.88 2
rs2073080
PARVB ; SAMM50
0.925 0.040 22 43998522 intron variant C/T snv 0.20 2
rs6006473
PARVB ; SAMM50
0.925 0.040 22 43997195 intron variant C/T snv 0.47 2
rs12483959
PNPLA3
1.000 22 43930116 intron variant G/A;C;T snv 2
rs2143571
SAMM50
0.827 0.080 22 43995806 intron variant G/A snv 0.25 2
rs2235776
SAMM50
0.925 0.040 22 43982119 intron variant C/T snv 0.24 2
rs3761472
SAMM50
0.925 0.040 22 43972242 missense variant A/G snv 0.21 0.18 2
rs738491
SAMM50 ; PNPLA3
0.882 0.040 22 43958231 intron variant C/T snv 0.34 2