Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs4437130 1.000 0.040 3 2035283 intergenic variant G/A snv 0.12 2
rs62561366 1.000 0.040 9 95555669 intergenic variant A/T snv 3.9E-02 2
rs1127354
ITPA
0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 2
rs10273639
PRSS1
0.776 0.280 7 142749077 upstream gene variant T/A;C snv 2
rs379742 1.000 0.040 X 106250703 intergenic variant G/A snv 0.17 1
rs1042636
CASR
0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02 1
rs1801725
CASR
0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 1
rs199695765
CPA2
0.925 0.160 7 130269008 stop gained C/T snv 8.8E-05 1.3E-04 1
rs11556218
IL16
0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 1
rs2995271
LOC101929279
0.925 0.040 10 30230903 regulatory region variant C/T snv 0.64 1
rs12014762
MORC4
0.882 0.080 X 106940440 intron variant C/T snv 0.14 1
rs12688220
MORC4
0.827 0.200 X 107001537 upstream gene variant C/T snv 0.19 1
rs6622126
MORC4
0.851 0.080 X 106956972 missense variant G/A snv 0.58 1
rs12008279
MORC4 ; CLDN2
0.882 0.080 X 106917472 intron variant A/G;T snv 1
rs7057398
MORC4 ; RIPPLY1 ; CLDN2
0.827 0.080 X 106901299 intron variant T/C snv 0.41 1
rs42490
RIPK2
0.882 0.160 8 89766285 intron variant G/A snv 0.60 1