Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11789015
BARX1
0.882 0.080 9 93953746 intron variant A/C;G snv 6
rs2687201 0.925 0.080 3 70879779 intergenic variant A/C;G snv 6
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
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
rs4800353 0.925 0.080 18 22074176 intergenic variant A/G snv 0.30 5
rs7632500
LOC107986152
0.925 0.080 3 168007561 downstream gene variant A/G snv 0.17 5
rs1548445
VPS35L
1.000 0.080 16 19680261 intron variant A/G snv 0.17 1
rs9823696 0.925 0.080 3 184065565 downstream gene variant A/G;T snv 2
rs4676893 0.882 0.080 3 70868488 intergenic variant A/T snv 0.61 3
rs66725070
ALDH1A2
1.000 0.080 15 57975219 intron variant ACAT/- delins 0.35 1
rs7852462
TMOD1
0.925 0.080 9 97548219 intron variant C/A;T snv 2
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs759412116
ERCC2
0.581 0.640 19 45352210 missense variant C/G;T snv 4.0E-06; 6.0E-05 55
rs121434569
EGFR-AS1 ; EGFR
0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs6214
LINC02456 ; HELLPAR ; IGF1
0.672 0.400 12 102399791 3 prime UTR variant C/T snv 0.45 26
rs536289169
GSTM1 ; GSTM2
0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04 13
rs9936833 0.882 0.160 16 86369512 intergenic variant C/T snv 0.64 6
rs764643047
OGG1
0.851 0.120 3 9750336 missense variant C/T snv 4.0E-06 5
rs2518720
CDKN2A
0.925 0.080 9 21978980 intron variant C/T snv 0.43 2
rs9918259
CEP72 ; TPPP
0.925 0.080 5 662977 3 prime UTR variant C/T snv 2.1E-03 2
rs4769585 1.000 0.080 13 27976441 downstream gene variant C/T snv 0.39 1
rs6449586 1.000 0.080 5 51339044 intergenic variant C/T snv 0.64 1