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
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 9
rs4820268
TMPRSS6
0.851 0.160 22 37073551 missense variant G/A;C snv 0.53; 4.0E-06 9
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 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
rs9494145 0.925 0.080 6 135111414 intergenic variant T/A;C snv 7
rs129128
H2BC4 ; H2AC6
6 26125114 intron variant C/T snv 0.91 7
rs4895441
LOC105378010
0.925 0.080 6 135105435 upstream gene variant A/G snv 0.21 7
rs12216125 0.925 0.120 6 25997230 intron variant C/T snv 0.26 6
rs130624 22 37042611 regulatory region variant G/T snv 0.47 6
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 6
rs9399137
HBS1L
0.851 0.320 6 135097880 intron variant T/C snv 0.20 6
rs9376092
LOC105378010
0.851 0.120 6 135106006 upstream gene variant C/A snv 0.24 6
rs228129
LOC112268295
22 37032558 upstream gene variant A/G snv 0.48 6
rs17342717
SLC17A1
6 25821542 intron variant C/T snv 6.1E-02 6
rs3887266
SLC17A3
0.925 0.120 6 25843518 intron variant C/T snv 8.9E-02 6
rs2413450
TMPRSS6
22 37074184 intron variant T/C snv 0.61 6
rs1320963 6 135122074 intergenic variant A/G snv 0.35 5
rs9295684 0.925 0.120 6 26069441 intergenic variant T/C snv 0.38 5
rs9379818 0.925 0.120 6 26022978 downstream gene variant G/A;T snv 5
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 5
rs1547247
HBS1L
6 135069698 intron variant G/A snv 0.22 5