Source: GWASDB ×
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 14
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
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 9
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 9
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs6457617 0.763 0.480 6 32696074 intergenic variant C/A;T snv 6
rs9275312 0.807 0.280 6 32697951 intergenic variant A/G snv 0.16 6
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 6
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 6
rs2856718 0.790 0.360 6 32702478 downstream gene variant C/T snv 0.34 5
rs7774434 0.807 0.360 6 32689801 TF binding site variant T/C snv 0.40 5
rs9272535
HLA-DQA2 ; LOC107986589 ; HLA-DQA1
0.827 0.280 6 32638979 synonymous variant G/A snv 3.0E-05 1.8E-03 5
rs7453920
HLA-DQB2
0.752 0.440 6 32762235 intron variant A/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
rs2228603
NCAN
0.790 0.360 19 19219115 missense variant C/A;T snv 2.8E-05; 5.9E-02 5
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 5
rs2647012 0.790 0.320 6 32696681 intergenic variant T/C snv 0.64 4
rs2856683 0.827 0.320 6 32687441 regulatory region variant T/A;C;G snv 0.25 4
rs3135363 0.776 0.360 6 32421871 intergenic variant A/G snv 0.24 4
rs5000634 0.851 0.200 6 32695787 intergenic variant A/G snv 0.39 4
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 4
rs548234
ATG5
0.763 0.360 6 106120159 intron variant C/T snv 0.76 4