Disease: Body mass index
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8082812 0.851 0.120 18 8522684 intergenic variant C/A snv 4.6E-02 16
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs9930333
FTO
0.882 0.120 16 53766065 intron variant T/C;G snv 7
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs9942416 5 75741470 intergenic variant C/G snv 0.53 9
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs2304130
ZNF101
1.000 0.080 19 19678719 splice region variant A/G snv 0.10 0.12 5
rs7607980
COBLL1
1.000 0.080 2 164694691 missense variant T/C snv 0.11 0.13 8
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs7200543
PDXDC1
16 15036113 synonymous variant A/G snv 0.35 0.30 6