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
rs10010131
WFS1
0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63 7
rs10247649
PDK4
0.925 0.080 7 95586935 non coding transcript exon variant A/G snv 0.43 2
rs1041981
LOC100287329 ; LTA
0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 25
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1044250
ANGPTL4
0.807 0.240 19 8371280 missense variant C/T snv 0.30 0.29 12
rs1049353
CNR1
0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
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
rs10738760 0.807 0.320 9 2691186 regulatory region variant A/G snv 0.56 7
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
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
rs11063069
CCND2-AS1
0.925 0.080 12 4265207 intron variant A/G snv 0.20 2
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs11646213 0.827 0.320 16 82609046 intergenic variant A/T snv 0.47 6
rs116843064
ANGPTL4
0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 16
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 9
rs11724758
FABP2
0.925 0.080 4 119318723 3 prime UTR variant G/A snv 0.47 2
rs11868035
RAI1 ; SREBF1
0.763 0.200 17 17811787 splice region variant G/A snv 0.45 0.33 14
rs12086634
HSD11B1-AS1 ; HSD11B1
0.827 0.280 1 209706914 intron variant T/G snv 0.21 0.20 6
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121909244
PPARG
0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06 11