Disease: Metabolic Syndrome X
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11600380 1.000 0.040 11 116799466 intergenic variant T/C snv 6.6E-02 3
rs11820589
BUD13
1.000 0.040 11 116763146 missense variant G/A snv 7.8E-02 0.10 5
rs12286037
ZPR1
1.000 0.040 11 116781491 intron variant C/T snv 0.11 6
rs12686004
ABCA1
1.000 0.040 9 104891145 intron variant G/A snv 9.1E-02 6
rs17410962 1.000 0.040 8 19990569 intergenic variant G/A snv 0.15 7
rs1797912
PPARG
1.000 0.040 3 12428740 intron variant A/C snv 0.33 3
rs2160669
ZPR1
1.000 0.040 11 116776891 3 prime UTR variant C/T snv 0.92 5
rs481843
LINC02702
1.000 0.040 11 116655150 non coding transcript exon variant C/T snv 8.8E-02 5
rs6494005
ALDH1A2 ; LIPC
1.000 0.040 15 58432325 non coding transcript exon variant A/G snv 0.38 5
rs6589567 1.000 0.040 11 116799960 intergenic variant A/C;G;T snv 4
rs711752
CETP
1.000 0.040 16 56962299 splice region variant G/A;C snv 10
rs7350481 0.882 0.040 11 116715567 regulatory region variant T/C snv 0.93 8
rs7575840 1.000 0.040 2 21050618 intergenic variant G/T snv 0.26 4
rs9939224
CETP
1.000 0.040 16 56968820 intron variant T/G snv 0.75 6
rs9987289
LOC157273
1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 10
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 8
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 9
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 13
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 11
rs2043085
ALDH1A2
0.827 0.080 15 58388755 intron variant T/C snv 0.54 9
rs3905000
ABCA1
0.925 0.080 9 104894789 intron variant G/A snv 0.14 5
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 10
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 12
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26 10
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 13