Disease: Body mass index
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs11651052
HNF1B
0.851 0.200 17 37742390 intron variant G/A snv 0.50 7
rs11658063
HNF1B
0.851 0.120 17 37743881 intron variant G/C;T snv 5