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: rs17782313
rs17782313 		34 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 0.040 1.000 4 2010 2018
dbSNP: rs7895833
rs7895833 		12 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 0.020 1.000 2 2015 2016
dbSNP: rs1996023
rs1996023 		3 0.925 0.120 4 45162620 intergenic variant T/A;G snv 0.010 1.000 1 2019 2019
dbSNP: rs2943650
rs2943650 		6 0.827 0.120 2 226241205 intergenic variant C/T snv 0.58 0.010 1.000 1 2019 2019
dbSNP: rs1501299
rs1501299
ADIPOQ ; ADIPOQ-AS1
52 0.597 0.720 3 186853334 intron variant G/C;T snv 0.010 1.000 1 2009 2009
dbSNP: rs4994
rs4994
ADRB3
65 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 0.020 1.000 2 2000 2015
dbSNP: rs2070600
rs2070600
AGER
82 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 0.010 1.000 1 2016 2016
dbSNP: rs2796749
rs2796749
AMD1
2 0.925 0.080 6 110873500 upstream gene variant C/A;G snv 0.80 0.010 1.000 1 2012 2012
dbSNP: rs2030323
rs2030323
BDNF
6 0.925 0.080 11 27706992 intron variant A/C snv 0.83 0.010 1.000 1 2017 2017
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 2012 2012
dbSNP: rs759834365
rs759834365
BDNF ; BDNF-AS
237 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 0.010 1.000 1 2012 2012
dbSNP: rs2501432
rs2501432
CNR2
16 0.716 0.480 1 23875430 missense variant T/C;G snv 0.62 0.010 1.000 1 2015 2015
dbSNP: rs35761398
rs35761398
CNR2
19 0.701 0.520 1 23875429 missense variant TT/CC mnv 0.010 1.000 1 2015 2015
dbSNP: rs879761216
rs879761216
CNR2
14 0.732 0.480 1 23875429 frameshift variant TT/C;T delins 0.010 1.000 1 2015 2015
dbSNP: rs997509
rs997509
ENPP1
6 0.827 0.200 6 131846837 intron variant C/T snv 5.3E-02 0.010 1.000 1 2009 2009
dbSNP: rs324419
rs324419
FAAH
3 0.925 0.120 1 46406314 stop gained T/A;C snv 0.87 0.010 1.000 1 2010 2010
dbSNP: rs324420
rs324420
FAAH
48 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 0.010 1.000 1 2010 2010
dbSNP: rs873978
rs873978
FAAH
1 1.000 0.080 1 46408231 intron variant C/T snv 5.2E-02 0.010 1.000 1 2010 2010
dbSNP: rs9939609
rs9939609
FTO
98 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.060 0.833 6 2012 2019
dbSNP: rs1421085
rs1421085
FTO
28 0.752 0.280 16 53767042 intron variant T/C snv 0.31 0.010 < 0.001 1 2014 2014
dbSNP: rs1558902
rs1558902
FTO
21 0.827 0.120 16 53769662 intron variant T/A snv 0.31 0.010 1.000 1 2017 2017
dbSNP: rs17817449
rs17817449
FTO
21 0.716 0.560 16 53779455 intron variant T/A;G snv 0.010 < 0.001 1 2014 2014
dbSNP: rs8057044
rs8057044
FTO
5 0.882 0.080 16 53778702 intron variant G/A snv 0.54 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 < 0.001 1 2005 2005
dbSNP: rs1800437
rs1800437
GIPR
13 0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 0.010 1.000 1 2010 2010