Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9936833 0.882 0.160 16 86369512 intergenic variant C/T snv 0.64 6
rs9918259
CEP72 ; TPPP
0.925 0.080 5 662977 3 prime UTR variant C/T snv 2.1E-03 2
rs9823696 0.925 0.080 3 184065565 downstream gene variant A/G;T snv 2
rs9668109
IKBIP
1.000 0.080 12 98617494 intron variant G/A snv 0.15 1
rs9257809
OR12D3 ; OR5V1
0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02 10
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs7852462
TMOD1
0.925 0.080 9 97548219 intron variant C/A;T snv 2
rs764643047
OGG1
0.851 0.120 3 9750336 missense variant C/T snv 4.0E-06 5
rs7632500
LOC107986152
0.925 0.080 3 168007561 downstream gene variant A/G snv 0.17 5
rs759412116
ERCC2
0.581 0.640 19 45352210 missense variant C/G;T snv 4.0E-06; 6.0E-05 55
rs7255
GDF7
0.925 0.080 2 20679060 3 prime UTR variant T/A;C snv 3
rs717746
CDX1
1.000 0.080 5 150176995 intron variant T/A;C;G snv 1
rs66725070
ALDH1A2
1.000 0.080 15 57975219 intron variant ACAT/- delins 0.35 1
rs6449586 1.000 0.080 5 51339044 intergenic variant C/T snv 0.64 1
rs62423175 0.925 0.080 6 61485463 intergenic variant G/A snv 2
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
rs491603
AGO3
1.000 0.080 1 36066715 3 prime UTR variant T/A;C snv 2
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs4800353 0.925 0.080 18 22074176 intergenic variant A/G snv 0.30 5
rs4769585 1.000 0.080 13 27976441 downstream gene variant C/T snv 0.39 1
rs4676893 0.882 0.080 3 70868488 intergenic variant A/T snv 0.61 3
rs3812863
CDX2
1.000 0.080 13 27971131 upstream gene variant G/A snv 0.48 1
rs3784262
ALDH1A2
0.882 0.160 15 57960908 intron variant T/A;C snv 6
rs3776083
SLC6A7
1.000 0.080 5 150188407 upstream gene variant G/A;C;T snv 1