Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10195252
rs10195252
COBLL1
7 0.925 0.080 2 164656581 intron variant T/C snv 0.48 0.010 1.000 1 2016 2016
dbSNP: rs1045895
rs1045895
LEPR ; LEPROT
2 0.925 0.080 1 65432298 3 prime UTR variant G/A;T snv 0.010 1.000 1 2016 2016
dbSNP: rs10822184
rs10822184
REEP3
2 1.000 10 63577393 intron variant T/C;G snv 0.010 1.000 1 2016 2016
dbSNP: rs10968576
rs10968576
LINGO2
10 0.882 0.120 9 28414341 intron variant A/G snv 0.26 0.010 1.000 1 2016 2016
dbSNP: rs1121980
rs1121980
FTO
18 0.807 0.240 16 53775335 intron variant G/A;C snv 0.010 1.000 1 2013 2013
dbSNP: rs1501299
rs1501299
ADIPOQ ; ADIPOQ-AS1
52 0.597 0.720 3 186853334 intron variant G/C;T snv 0.010 1.000 1 2016 2016
dbSNP: rs17300539
rs17300539
ADIPOQ
11 0.752 0.320 3 186841671 upstream gene variant G/A snv 5.3E-02 0.010 1.000 1 2016 2016
dbSNP: rs1801282
rs1801282
PPARG
131 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 1.000 1 2016 2016
dbSNP: rs1805092
rs1805092
LEPR
2 0.925 0.080 1 65570758 missense variant A/G snv 0.010 1.000 1 2016 2016
dbSNP: rs2023239
rs2023239
CNR1
20 0.724 0.160 6 88150763 intron variant T/C snv 0.21 0.010 < 0.001 1 2012 2012
dbSNP: rs2229616
rs2229616
MC4R
22 0.732 0.200 18 60372043 missense variant C/T snv 1.6E-02 1.6E-02 0.010 1.000 1 2010 2010
dbSNP: rs2419621
rs2419621
ACSL5
3 0.925 0.080 10 112375255 non coding transcript exon variant C/T snv 0.23 0.010 1.000 1 2016 2016
dbSNP: rs3782886
rs3782886
BRAP
22 0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 0.010 1.000 1 2019 2019
dbSNP: rs3846662
rs3846662
HMGCR
12 0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 0.010 1.000 1 2014 2014
dbSNP: rs3846663
rs3846663
HMGCR ; CERT1
7 0.882 0.120 5 75359901 intron variant C/T snv 0.35 0.010 1.000 1 2014 2014
dbSNP: rs3923113
rs3923113 		3 0.882 0.120 2 164645339 intergenic variant A/C;G;T snv 0.010 1.000 1 2016 2016
dbSNP: rs4425043
rs4425043
GCKR
3 0.882 0.120 2 27510585 intron variant G/A;T snv 0.010 1.000 1 2011 2011
dbSNP: rs4917
rs4917
AHSG
9 0.790 0.160 3 186619924 missense variant T/C snv 0.68 0.68 0.010 1.000 1 2017 2017
dbSNP: rs4994
rs4994
ADRB3
65 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 0.010 1.000 1 2018 2018
dbSNP: rs5934505
rs5934505 		10 0.776 0.120 X 8945785 intergenic variant T/A;C snv 0.010 1.000 1 2016 2016
dbSNP: rs6265
rs6265
BDNF ; BDNF-AS
272 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.010 1.000 1 2019 2019
dbSNP: rs696217
rs696217
GHRL ; GHRLOS
32 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 0.010 1.000 1 2019 2019
dbSNP: rs7799039
rs7799039
LOC105375494
33 0.649 0.560 7 128238730 upstream gene variant G/A;C snv 0.010 1.000 1 2018 2018
dbSNP: rs806381
rs806381
CNR1
2 0.925 0.080 6 88156182 intron variant A/G snv 0.32 0.010 < 0.001 1 2012 2012
dbSNP: rs8179206
rs8179206
GCKR
1 1.000 2 27497575 missense variant A/G snv 1.9E-03 7.2E-04 0.010 1.000 1 2011 2011