Disease: Metabolic Syndrome X
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1000283
HSD11B1 ; HSD11B1-AS1
0.925 0.080 1 209721316 intron variant G/A snv 0.18 2
rs10247649
PDK4
0.925 0.080 7 95586935 non coding transcript exon variant A/G snv 0.43 2
rs11063069
CCND2-AS1
0.925 0.080 12 4265207 intron variant A/G snv 0.20 2
rs11724758
FABP2
0.925 0.080 4 119318723 3 prime UTR variant G/A snv 0.47 2
rs12691
CEBPA
0.925 0.080 19 33300221 3 prime UTR variant G/A snv 0.16 2
rs3212183
HNF4A ; MIR3646
0.925 0.080 20 44406498 intron variant C/T snv 0.58 2
rs5945326 0.925 0.080 X 153634467 regulatory region variant A/G snv 0.25 2
rs6947830 0.925 0.080 7 15025359 intergenic variant G/A;C snv 2
rs745975
HNF4A
0.925 0.080 20 44406053 splice region variant C/T snv 0.20 0.18 2
rs1051295
KCNB1 ; LOC105372649
0.925 0.080 20 49372368 3 prime UTR variant A/G snv 0.22 3
rs1052717
SREBF2
0.925 0.080 22 41885425 intron variant A/G snv 0.62 3
rs13283456
PTGES2
0.925 0.080 9 128122474 missense variant C/A;T snv 4.0E-06; 0.13 3
rs1411766
LOC101927627
0.882 0.160 13 109599813 intron variant G/A;T snv 3
rs1423096 0.925 0.080 19 7674291 upstream gene variant T/C snv 0.92 3
rs163182
KCNQ1
0.882 0.160 11 2822986 intron variant G/A;C snv 3
rs1801276
IRS1
0.882 0.160 2 226797205 missense variant C/G snv 1.4E-02 1.3E-02 3
rs2291726
GIP
0.925 0.080 17 48961892 intron variant T/A;C snv 3
rs2425637
HNF4A ; HNF4A-AS1
0.925 0.080 20 44395409 intron variant G/T snv 0.42 3
rs726344
FNDC5
0.882 0.120 1 32867503 intron variant G/A snv 0.16 3
rs7612463
UBE2E2
0.925 0.080 3 23294959 intron variant C/A;G snv 3
rs12221497
NR1H3
0.882 0.160 11 47259102 splice region variant G/A snv 0.11 4
rs17373080
NR1H2
0.851 0.160 19 50376267 5 prime UTR variant C/G snv 0.29 4
rs1884051
ESR1
0.882 0.080 6 151962144 intron variant G/A snv 0.60 4
rs2270565
UCP1
0.882 0.080 4 140562317 missense variant T/A snv 8.9E-02 6.5E-02 4
rs2291725
GIP
0.882 0.120 17 48961770 missense variant T/C snv 0.50 0.40 4