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
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 10
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs9257809
OR12D3 ; OR5V1
0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02 4
rs9936833 0.882 0.160 16 86369512 intergenic variant C/T snv 0.64 3
rs10419226
CRTC1
0.925 0.080 19 18692362 intron variant T/G snv 0.67 2
rs2687201 0.925 0.080 3 70879779 intergenic variant A/C;G snv 1
rs6449586 1.000 0.080 5 51339044 intergenic variant C/T snv 0.64 1
rs3784262
ALDH1A2
0.882 0.160 15 57960908 intron variant T/A;C snv 1
rs11789015
BARX1
0.882 0.080 9 93953746 intron variant A/C;G snv 1