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
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 12
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 10
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 9
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 8
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 7
rs12663103
GPSM3
0.851 0.240 6 32193547 intron variant T/C snv 6.1E-02 7
rs477515
HLA-DRB1
0.790 0.400 6 32601914 intergenic variant G/A snv 0.27 7
rs9275141 0.827 0.240 6 32683340 intergenic variant T/G snv 0.50 6
rs652888
EHMT2-AS1 ; EHMT2 ; LOC107986588 ; CYP21A2
0.776 0.480 6 31883457 non coding transcript exon variant A/G snv 0.18 0.20 6
rs2395174 0.827 0.320 6 32437101 upstream gene variant T/G snv 0.24 5
rs2517459 0.882 0.160 6 30929245 downstream gene variant T/C snv 0.74 5
rs2856718 0.790 0.360 6 32702478 downstream gene variant C/T snv 0.34 5
rs3130542 0.827 0.160 6 31264334 downstream gene variant A/G snv 0.81 5
rs3130779 0.925 0.080 6 30904426 upstream gene variant A/C;G;T snv 5
rs1265115
CCHCR1
0.925 0.080 6 31149298 non coding transcript exon variant C/A;T snv 5
rs3131034
DDR1
0.925 0.080 6 30886019 intron variant G/A snv 0.75 5
rs9277554
HLA-DPB1
0.790 0.520 6 33087761 3 prime UTR variant C/T snv 0.38 5
rs7453920
HLA-DQB2
0.752 0.440 6 32762235 intron variant A/G;T snv 5
rs9268645
HLA-DRA
0.827 0.360 6 32440750 intron variant C/G;T snv 5
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 5
rs2596542
MICA-AS1 ; MICA
0.724 0.200 6 31398818 upstream gene variant C/T snv 0.41 5