Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs4580704
CLOCK
0.790 0.200 4 55460540 intron variant G/C snv 0.69 13
rs11932595
CLOCK
0.827 0.160 4 55457430 intron variant A/G;T snv 12
rs1984112
CD36
0.807 0.280 7 80613604 intron variant A/G snv 0.33 8
rs6782181
MRAS
0.851 0.160 3 138386212 intron variant G/A;C snv 6
rs804280
GATA4
0.882 0.120 8 11755189 intron variant C/A;G snv 6
rs4149081
SLCO1B1
1.000 0.040 12 21225087 intron variant G/A snv 0.18 5
rs2235543
HSD11B1-AS1 ; HSD11B1
0.925 0.080 1 209687323 intron variant T/A;C snv 4
rs3761740
HMGCR
0.882 0.160 5 75336308 intron variant C/A snv 8.2E-02 4
rs17222772
ALOX5AP
0.925 0.120 13 30737959 intron variant A/T snv 3
rs1746661
FNDC5
0.925 0.080 1 32869438 intron variant G/A;T snv 3
rs1468271
LOC107986777 ; NPY
1.000 0.040 7 24287362 intron variant C/T snv 0.97 2
rs4072032
PECAM1
1.000 0.040 17 64378896 intron variant G/A snv 0.40 2
rs4393158
HSD11B1-AS1
1.000 0.040 1 209678552 intron variant A/G;T snv 2
rs6066394
NCOA3
1.000 0.040 20 47581409 intron variant C/T snv 0.29 2
rs4823613
PPARA
1.000 0.040 22 46202410 intron variant A/G snv 0.30 1
rs515135 0.807 0.160 2 21063185 intergenic variant T/C snv 0.73 9
rs7566605
LOC107985940
0.752 0.320 2 118078449 regulatory region variant C/G snv 0.70 11
rs2228671
LDLR
0.790 0.160 19 11100236 stop gained C/A;G;T snv 1.6E-05; 8.9E-02 14
rs368657165
LDLR
0.827 0.080 19 11107436 stop gained G/A;T snv 4.0E-05 7
rs138947766
LDLR
0.851 0.080 19 11116883 stop gained G/A;C snv 8.0E-06 6
rs144172724
LDLR
0.851 0.080 19 11102774 stop gained G/A;T snv 1.6E-05 6
rs879254597
LDLR
0.851 0.120 19 11105528 stop gained G/A;T snv 4