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
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs4994
ADRB3
0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs324420
FAAH
0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs7799039
LOC105375494
0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs696217
GHRL ; GHRLOS
0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 22
rs2229616
MC4R
0.732 0.200 18 60372043 missense variant C/T snv 1.6E-02 1.6E-02 22
rs2023239
CNR1
0.724 0.160 6 88150763 intron variant T/C snv 0.21 20
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 18
rs3846662
HMGCR
0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 12
rs17300539
ADIPOQ
0.752 0.320 3 186841671 upstream gene variant G/A snv 5.3E-02 11
rs5934505 0.776 0.120 X 8945785 intergenic variant T/A;C snv 10
rs10968576
LINGO2
0.882 0.120 9 28414341 intron variant A/G snv 0.26 10
rs4917
AHSG
0.790 0.160 3 186619924 missense variant T/C snv 0.68 0.68 9
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 7
rs3846663
HMGCR ; CERT1
0.882 0.120 5 75359901 intron variant C/T snv 0.35 7
rs3923113 0.882 0.120 2 164645339 intergenic variant A/C;G;T snv 3
rs2419621
ACSL5
0.925 0.080 10 112375255 non coding transcript exon variant C/T snv 0.23 3
rs4425043
GCKR
0.882 0.120 2 27510585 intron variant G/A;T snv 3
rs806381
CNR1
0.925 0.080 6 88156182 intron variant A/G snv 0.32 2