Disease: Metabolic Syndrome X
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10738760 0.807 0.320 9 2691186 regulatory region variant A/G snv 0.56 7
rs10830962 0.851 0.160 11 92965261 upstream gene variant C/A;G;T snv 7
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs11646213 0.827 0.320 16 82609046 intergenic variant A/T snv 0.47 6
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 10
rs1423096 0.925 0.080 19 7674291 upstream gene variant T/C snv 0.92 3
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs1800592 0.807 0.200 4 140572807 upstream gene variant T/C snv 0.40 8
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs5015480 0.851 0.120 10 92705802 downstream gene variant C/T snv 0.42 9
rs5945326 0.925 0.080 X 153634467 regulatory region variant A/G snv 0.25 2
rs6921438 0.776 0.360 6 43957870 intergenic variant G/A;C snv 10
rs6947830 0.925 0.080 7 15025359 intergenic variant G/A;C snv 2
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 17
rs9282541
ABCA1
0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 13
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 9
rs17300539
ADIPOQ
0.752 0.320 3 186841671 upstream gene variant G/A snv 5.3E-02 11
rs266729
ADIPOQ
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs822396
ADIPOQ
0.732 0.400 3 186849088 intron variant G/A snv 0.81 16
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs185847354
ADIPOQ ; ADIPOQ-AS1
0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05 11