Disease: Metabolic Syndrome X
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1040288
NR3C2
1.000 0.040 4 148126966 intron variant G/C snv 0.49 3
rs11099680
NR3C2
1.000 0.040 4 148182095 intron variant G/A snv 0.78 2
rs2288775
NEDD4L
1.000 0.040 18 58316132 intron variant A/G snv 0.25 2
rs711752
CETP
1.000 0.040 16 56962299 splice region variant G/A;C snv 10
rs768925824
LDLR
0.925 0.040 19 11110693 missense variant G/A snv 4.0E-06 4
rs12149545 0.851 0.080 16 56959249 upstream gene variant G/A snv 0.23 7
rs137853240
HNF1A
0.807 0.080 12 120994405 missense variant G/A snv 1.4E-05 8
rs148446907
AGT
0.925 0.080 1 230710026 synonymous variant G/A;C snv 1.2E-05 3
rs3748024
CHCHD5
0.925 0.080 2 112588836 3 prime UTR variant C/G snv 0.41 0.35 3
rs6993
GOT2
0.925 0.080 16 58707463 3 prime UTR variant A/G snv 0.59 3
rs8057044
FTO
0.882 0.080 16 53778702 intron variant G/A snv 0.54 5
rs1175543
PPARG
0.851 0.120 3 12424934 intron variant A/G snv 0.28 5
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 21
rs4757268
PDE3B
0.827 0.120 11 14789216 synonymous variant A/G snv 0.63 0.64 6
rs568401628
ACE
0.882 0.120 17 63497280 missense variant C/T snv 4.5E-05 7.0E-06 4
rs121909244
PPARG
0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06 11
rs1337503417
KRT16
0.790 0.160 17 41612325 missense variant G/T snv 4.0E-06 12
rs146052672
HMGA1
0.851 0.160 6 34242693 intron variant -/C delins 5
rs1554483
CLOCK
0.882 0.160 4 55455650 intron variant C/G snv 0.33 5
rs185847354
ADIPOQ ; ADIPOQ-AS1
0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05 11
rs2074192
ACE2
0.827 0.160 X 15564667 intron variant C/T snv 0.40 9
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs3782889
MYL2
0.851 0.160 12 110912851 intron variant A/G snv 7.1E-02 5
rs4864548
CLOCK
0.827 0.160 4 55547636 non coding transcript exon variant G/A snv 0.33 8
rs5068
NPPA ; NPPA-AS1 ; CLCN6
0.776 0.160 1 11845917 3 prime UTR variant A/G;T snv 13