Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7799039
LOC105375494
0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs806381
CNR1
0.925 0.080 6 88156182 intron variant A/G snv 0.32 2
rs8179206
GCKR
1.000 2 27497575 missense variant A/G snv 1.9E-03 7.2E-04 1
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98