Disease: Body mass index
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs1481012
ABCG2
0.882 0.200 4 88117930 intron variant A/G snv 8.9E-02 6
rs4148155
ABCG2
0.882 0.200 4 88133515 intron variant A/G snv 8.7E-02 5
rs11663816 18 60208994 intergenic variant T/C snv 0.20 4
rs506338
NRXN2
0.925 0.120 11 64673448 intron variant T/C snv 0.52 4
rs60808706
KCNQ1
11 2836003 intron variant G/A snv 0.12 4
rs11084786
LINC01801
19 34791277 intron variant A/G snv 0.38 2
rs12135191 1 236307434 regulatory region variant C/G;T snv 2
rs12693043 2 174512837 intergenic variant C/T snv 0.36 2
rs13116011 4 136424394 intergenic variant T/A;C snv 2
rs16886173 8 114608231 intergenic variant T/G snv 7.5E-02 2
rs1917861 11 80678655 intergenic variant A/G;T snv 2
rs35198068
TCF7L2
10 112995025 intron variant T/C snv 0.29 2
rs7305242 12 111818958 downstream gene variant T/C snv 5.0E-02 2
rs898534
RBFOX3
17 79277431 intron variant G/A snv 8.7E-02 2