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: rs52804924
rs52804924
MC4R
2 0.925 0.080 18 60371454 missense variant G/A;T snv 8.0E-06 0.010 1.000 1 2003 2003
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: rs1232898090
rs1232898090
PPARA
40 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 0.020 1.000 2 2005 2006
dbSNP: rs162430
rs162430
PYY
1 1.000 0.080 17 43953041 3 prime UTR variant G/A snv 0.23 0.010 1.000 1 2007 2007
dbSNP: rs1800849
rs1800849
UCP3
5 0.851 0.160 11 74009120 upstream gene variant G/A;T snv 0.010 1.000 1 2007 2007
dbSNP: rs659366
rs659366
UCP2
17 0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 0.010 1.000 1 2007 2007
dbSNP: rs6857715
rs6857715
NPY2R ; LOC107986321
5 0.827 0.160 4 155208030 non coding transcript exon variant C/A;T snv 0.010 1.000 1 2007 2007
dbSNP: rs149106723
rs149106723
NMU
1 1.000 0.080 4 55599178 missense variant G/A snv 1.6E-05 4.2E-05 0.020 1.000 2 2006 2009
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: 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: 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
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: rs2016266
rs2016266
SP7
3 1.000 0.080 12 53334171 intron variant G/A;C snv 0.010 1.000 1 2011 2011
dbSNP: rs738409
rs738409
PNPLA3
88 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 0.010 1.000 1 2011 2011
dbSNP: rs2241423
rs2241423
MAP2K5
7 0.882 0.120 15 67794500 intron variant G/A snv 0.29 0.010 1.000 1 2012 2012
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: rs4704397
rs4704397
PDE8B
13 0.807 0.200 5 77222617 intron variant G/A snv 0.54 0.010 1.000 1 2012 2012
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: rs2285053
rs2285053
MMP2
15 0.752 0.320 16 55478465 intron variant C/T snv 0.12 0.010 1.000 1 2013 2013
dbSNP: rs243865
rs243865
MMP2
48 0.600 0.640 16 55477894 intron variant C/T snv 0.19 0.010 1.000 1 2013 2013
dbSNP: rs854566
rs854566
PON1
2 0.925 0.080 7 95319437 intron variant A/G snv 0.78 0.010 1.000 1 2013 2013
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