Source: BEFREE ×
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: rs121913564
rs121913564
MC4R
2 0.882 0.080 18 60371403 missense variant A/C snv 2.0E-05 1.4E-05 0.010 1.000 1 2012 2012
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 1997 2007
dbSNP: rs201408477
rs201408477
POMC
2 0.925 0.080 2 25161455 missense variant A/G snv 1.8E-04 1.6E-04 0.010 1.000 1 2015 2015
dbSNP: rs2239607
rs2239607
ACACB
3 0.925 0.120 12 109209475 intron variant A/G snv 0.14 0.010 1.000 1 2011 2011
dbSNP: rs540467809
rs540467809
QPCTL
2 0.925 0.080 19 45698838 missense variant A/G snv 1.0E-03 2.2E-04 0.010 1.000 1 2015 2015
dbSNP: rs564343
rs564343
PACS1
2 0.925 0.080 11 66127695 intron variant A/G snv 0.46 0.010 1.000 1 2017 2017
dbSNP: rs6020846
rs6020846
CTNNBL1
2 0.925 0.080 20 37777265 intron variant A/G snv 0.13 0.010 1.000 1 2009 2009
dbSNP: rs746906443
rs746906443
MC4R
2 0.925 0.080 18 60371868 missense variant A/G snv 4.0E-06 0.010 1.000 1 2012 2012
dbSNP: rs917346005
rs917346005
CADM2
2 0.925 0.080 3 85912502 missense variant A/G snv 0.010 1.000 1 2015 2015
dbSNP: rs9930506
rs9930506
FTO
9 0.776 0.360 16 53796553 intron variant A/G snv 0.36 0.010 1.000 1 2016 2016
dbSNP: rs10487818
rs10487818
NAMPT
1 1.000 0.080 7 106269615 intron variant A/T snv 1.1E-02 0.010 1.000 1 2009 2009
dbSNP: rs28362491
rs28362491
NFKB1 ; LOC105377621
56 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 0.020 1.000 2 2016 2018
dbSNP: rs324420
rs324420
FAAH
48 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 0.020 0.500 2 2008 2015
dbSNP: rs35859249
rs35859249
TBC1D1
6 0.807 0.200 4 37902468 missense variant C/A;T snv 4.0E-06; 9.7E-02 0.010 1.000 1 2008 2008
dbSNP: rs738409
rs738409
PNPLA3
80 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 0.020 1.000 2 2010 2012
dbSNP: rs1801282
rs1801282
PPARG
127 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 1.000 1 2012 2012
dbSNP: rs1805192
rs1805192
PPARG
117 0.510 0.840 3 12379739 missense variant C/G snv 0.010 1.000 1 2012 2012
dbSNP: rs7566605
rs7566605
LOC107985940
11 0.752 0.320 2 118078449 regulatory region variant C/G snv 0.70 0.010 1.000 1 2008 2008
dbSNP: rs1800949
rs1800949
ENPP1
1 1.000 0.080 6 131807424 upstream gene variant C/G;T snv 0.18 0.010 1.000 1 2008 2008
dbSNP: rs1805097
rs1805097
IRS2
21 0.689 0.360 13 109782884 missense variant C/G;T snv 0.35 0.010 1.000 1 2003 2003
dbSNP: rs1322837244
rs1322837244
QPCTL
2 0.925 0.080 19 45698622 missense variant C/T snv 0.010 1.000 1 2015 2015
dbSNP: rs2076349
rs2076349
LAMB3
3 0.882 0.120 1 209626885 missense variant C/T snv 0.13 0.13 0.010 1.000 1 2016 2016
dbSNP: rs2229616
rs2229616
MC4R
18 0.732 0.200 18 60372043 missense variant C/T snv 1.6E-02 1.6E-02 0.010 1.000 1 2008 2008
dbSNP: rs3856806
rs3856806
PPARG
41 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 0.010 1.000 1 2012 2012
dbSNP: rs4148325
rs4148325
UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A6 ; UGT1A5 ; UGT1A9 ; UGT1A4 ; UGT1A1 ; UGT1A3
1 0.851 0.080 2 233764663 intron variant C/T snv 0.36 0.010 1.000 1 2015 2015