Disease: Obesity, Morbid
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
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
rs2229616
MC4R
0.732 0.200 18 60372043 missense variant C/T snv 1.6E-02 1.6E-02 22
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 16
rs6013029
CTNNBL1
0.882 0.160 20 37771178 intron variant G/T snv 0.12 5
rs7001819
LOC105379243
0.925 0.080 8 11792966 upstream gene variant T/C snv 0.35 4