Source: ALL
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 0.10 226
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
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
rs121434569
EGFR-AS1 ; EGFR
0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs759412116
ERCC2
0.581 0.640 19 45352210 missense variant C/G;T snv 4.0E-06; 6.0E-05 55
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 30
rs1202989817
SOD1 ; LOC102724449
0.716 0.360 21 31659813 missense variant T/C;G snv 8.0E-06 7.0E-06 18
rs536289169
GSTM1 ; GSTM2
0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04 13
rs764643047
OGG1
0.851 0.120 3 9750336 missense variant C/T snv 4.0E-06 5
rs1263178238
VSIG10L
0.925 0.080 19 51338047 missense variant T/C snv 2.6E-05 4.9E-05 2
rs150885638
DLG5
1.000 0.080 10 77842176 missense variant T/C snv 6.1E-04 3.5E-04 1
rs10108511
LINC00208
0.925 0.080 8 11578007 non coding transcript exon variant T/A;C snv 2
rs2409797
LINC00208
1.000 0.080 8 11576271 non coding transcript exon variant T/C;G snv 1
rs6214
LINC02456 ; HELLPAR ; IGF1
0.672 0.400 12 102399791 3 prime UTR variant C/T snv 0.45 26
rs3088440
CDKN2A ; CDKN2A-DT
0.776 0.240 9 21968160 3 prime UTR variant G/A snv 0.13 12
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
rs491603
AGO3
1.000 0.080 1 36066715 3 prime UTR variant T/A;C snv 2
rs9918259
CEP72 ; TPPP
0.925 0.080 5 662977 3 prime UTR variant C/T snv 2.1E-03 2
rs1979654 0.925 0.080 16 86363229 TF binding site variant G/C snv 0.55 2
rs2671828 1.000 0.080 17 35404745 upstream gene variant T/C snv 0.55 1