Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs536289169
GSTM1 ; GSTM2
0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04 13
rs491603
AGO3
1.000 0.080 1 36066715 3 prime UTR variant T/A;C snv 2
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs11901649
APOB
0.882 0.080 2 21027351 intron variant G/A;C;T snv 3
rs7255
GDF7
0.925 0.080 2 20679060 3 prime UTR variant T/A;C snv 3
rs3072
GDF7
0.925 0.160 2 20678646 3 prime UTR variant T/C snv 0.30 2
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs2687201 0.925 0.080 3 70879779 intergenic variant A/C;G snv 6
rs7632500
LOC107986152
0.925 0.080 3 168007561 downstream gene variant A/G snv 0.17 5
rs764643047
OGG1
0.851 0.120 3 9750336 missense variant C/T snv 4.0E-06 5
rs4676893 0.882 0.080 3 70868488 intergenic variant A/T snv 0.61 3
rs2687202 0.925 0.080 3 70880832 regulatory region variant T/C snv 0.64 2
rs9823696 0.925 0.080 3 184065565 downstream gene variant A/G;T snv 2
rs9918259
CEP72 ; TPPP
0.925 0.080 5 662977 3 prime UTR variant C/T snv 2.1E-03 2
rs3776082 1.000 0.080 5 150164482 upstream gene variant G/A;C snv 1
rs3776083
SLC6A7
1.000 0.080 5 150188407 upstream gene variant G/A;C;T snv 1
rs6449586 1.000 0.080 5 51339044 intergenic variant C/T snv 0.64 1
rs717746
CDX1
1.000 0.080 5 150176995 intron variant T/A;C;G snv 1
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs9257809
OR12D3 ; OR5V1
0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02 10
rs62423175 0.925 0.080 6 61485463 intergenic variant G/A snv 2