Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs869109213
NOS3
0.790 0.200 7 150997269 intron variant GGGGGTGAGGAAGTCTAGACCTGCTGCG/A delins 10
rs12413409
CNNM2
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 9
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14 9
rs320
LPL
0.827 0.200 8 19961566 intron variant T/A;G snv 9
rs57137919
ABCG1 ; LOC105372814
0.776 0.160 21 42218908 intron variant G/A snv 0.14 9
rs10116277
CDKN2B-AS1
0.827 0.160 9 22081398 intron variant G/T snv 0.62 8
rs1041740
SOD1
0.807 0.320 21 31667849 intron variant C/T snv 0.24 8
rs243866
MMP2
0.827 0.120 16 55477625 intron variant G/A snv 0.19 8
rs2781666
ARG1
0.790 0.280 6 131572419 intron variant G/T snv 0.45 8
rs374778785
RORA-AS1 ; RORA
0.790 0.240 15 60627500 intron variant T/A snv 4.2E-05 8
rs3807306
IRF5
0.776 0.320 7 128940626 intron variant G/A;T snv 8
rs10118757
MTAP
0.827 0.120 9 21853340 intron variant A/G snv 0.26 7
rs10432782
SOD1
0.807 0.160 21 31664078 intron variant T/G snv 0.19 7
rs6922269
MTHFD1L
0.807 0.200 6 150931849 intron variant G/A snv 0.35 7
rs7944926
NADSYN1
0.807 0.200 11 71454579 intron variant A/G snv 0.54 7
rs1234313
TNFSF4
0.807 0.400 1 173197108 intron variant A/G snv 0.72 6
rs12746200
PLA2G4A
0.851 0.160 1 186880054 intron variant A/G snv 7.3E-02 6
rs2162679
IGF1
0.851 0.240 12 102477481 intron variant C/G;T snv 6
rs2453021
TNFRSF9
0.807 0.080 1 7929506 intron variant C/A;T snv 6
rs264
LPL
0.882 0.080 8 19955669 intron variant G/A snv 0.14 6
rs4788102
SH2B1
0.851 0.160 16 28862077 intron variant G/A snv 0.34 6
rs518394
CDKN2B-AS1
0.827 0.160 9 22019674 intron variant G/C snv 0.30 6
rs72743461
SMAD3
0.827 0.160 15 67149412 intron variant C/A;T snv 6
rs9551963
ALOX5AP
0.851 0.160 13 30758410 intron variant A/C;T snv 6
rs9632884
CDKN2B-AS1
0.851 0.160 9 22072302 intron variant G/A;C snv 6