Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11071657 1.000 0.040 15 62141763 regulatory region variant A/G snv 0.31 1
rs12513649 0.851 0.160 5 173045049 regulatory region variant C/G;T snv 1
rs6564851 0.882 0.120 16 81230992 intergenic variant T/G snv 0.48 1
rs7193788 0.925 0.120 16 82622555 upstream gene variant A/G snv 0.16 1
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 1
rs137852671
ABCC8
0.790 0.160 11 17394295 missense variant C/T snv 1
rs28938469
ABCC8
0.925 0.160 11 17395659 missense variant G/A snv 1
rs735949
ACSL1
0.925 0.080 4 184795078 intron variant T/C snv 0.10 1
rs4994
ADRB3
0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 1
rs3789678
AGT
1.000 0.040 1 230713736 intron variant C/T snv 0.15 1
rs35457250
AHSG
0.925 0.080 3 186620775 missense variant C/T snv 9.0E-03 8.1E-03 1
rs796065047
APPL1
0.882 0.080 3 57238111 missense variant G/A snv 4.0E-06 1
rs869320673
APPL1
0.882 0.080 3 57260016 stop gained T/A snv 1
rs4838605
ARHGAP22
0.882 0.160 10 48491914 intron variant C/T snv 0.38 1
rs55758736
BLK
0.851 0.120 8 11548067 missense variant G/A snv 1.2E-02 1.5E-02 1
rs6929846
BTN2A1
0.827 0.160 6 26458037 5 prime UTR variant T/C snv 0.70 1
rs11212617
C11orf65
0.827 0.200 11 108412434 intron variant C/A snv 0.49 1
rs4151667
CFB ; CYP21A2
0.790 0.320 6 31946247 missense variant T/A snv 3.9E-02 3.4E-02 1
rs12144939
CFH
0.925 0.080 1 196729815 intron variant G/A;T snv 1
rs5063
CLCN6 ; NPPA-AS1 ; NPPA
0.763 0.280 1 11847591 missense variant C/T snv 5.6E-02 5.3E-02 1
rs9925481
CLEC16A
0.882 0.160 16 11003622 intron variant C/G;T snv 1
rs2279590
CLU
0.851 0.200 8 27598736 non coding transcript exon variant T/C snv 0.69 1
rs2073618
COLEC10 ; TNFRSF11B
0.716 0.480 8 118951813 missense variant G/C snv 0.52 0.60 1
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 1
rs36071027
EBF1
0.925 0.080 5 159017266 intron variant C/T snv 0.29 1