Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G 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
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 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
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 9
rs4820268
TMPRSS6
0.851 0.160 22 37073551 missense variant G/A;C snv 0.53; 4.0E-06 9
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 8
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 8
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 8
rs129128
H2BC4 ; H2AC6
6 26125114 intron variant C/T snv 0.91 7
rs130624 22 37042611 regulatory region variant G/T snv 0.47 6
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 6
rs9399137
HBS1L
0.851 0.320 6 135097880 intron variant T/C snv 0.20 6
rs228129
LOC112268295
22 37032558 upstream gene variant A/G snv 0.48 6
rs2413450
TMPRSS6
22 37074184 intron variant T/C snv 0.61 6
rs198846
H1-6
6 26107235 downstream gene variant A/G;T snv 5
rs11089823 22 37113139 upstream gene variant T/C snv 0.28 4
rs11089824 22 37113146 upstream gene variant A/C;T snv 4
rs198833 6 26114280 downstream gene variant G/A snv 0.87 4
rs218237 4 54528005 intergenic variant C/T snv 0.18 4
rs763668 22 37115036 intergenic variant C/G;T snv 4
rs3218097
CCND3
6 41937537 intron variant G/A;T snv 4
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 4
rs16926246
HK1
10 69333636 intron variant C/T snv 0.12 4