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: rs199951903
rs199951903
CYTB ; ND6
2 0.925 0.120 MT 15497 missense variant G/A snv 0.010 1.000 1 2006 2006
dbSNP: rs738409
rs738409
PNPLA3
88 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 0.020 1.000 2 2010 2012
dbSNP: rs6013029
rs6013029
CTNNBL1
5 0.882 0.160 20 37771178 intron variant G/T snv 0.12 0.010 1.000 1 2009 2009
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: rs1322837244
rs1322837244
QPCTL
2 0.925 0.080 19 45698622 missense variant C/T snv 0.010 1.000 1 2015 2015
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: rs121913564
rs121913564
MC4R
3 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: rs121913566
rs121913566
MC4R
2 0.925 0.080 18 60372165 missense variant T/C snv 4.0E-06 0.010 1.000 1 2000 2000
dbSNP: rs13447331
rs13447331
MC4R
2 0.925 0.080 18 60371970 missense variant G/A snv 1.7E-04 7.7E-05 0.010 1.000 1 2014 2014
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 2008 2008
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: rs768916374
rs768916374
MC4R
1 1.000 0.080 18 60371880 missense variant T/G snv 4.0E-06 0.010 1.000 1 2008 2008
dbSNP: rs9930506
rs9930506
FTO
16 0.776 0.360 16 53796553 intron variant A/G snv 0.36 0.010 1.000 1 2016 2016
dbSNP: rs9932411
rs9932411
FTO
1 1.000 0.080 16 53971251 intron variant C/T snv 0.50 0.010 1.000 1 2013 2013
dbSNP: rs9939609
rs9939609
FTO
98 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2012 2012
dbSNP: rs1805097
rs1805097
IRS2
22 0.689 0.360 13 109782884 missense variant C/G;T snv 0.35 0.010 1.000 1 2003 2003
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: rs2268388
rs2268388
ACACB
6 0.851 0.200 12 109205840 intron variant G/A snv 0.14 0.010 1.000 1 2011 2011
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: 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: rs660339
rs660339
UCP2
24 0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43 0.010 1.000 1 2007 2007
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 2019 2019
dbSNP: rs1064891
rs1064891
PFKFB3
2 0.925 0.080 10 6234611 3 prime UTR variant T/C snv 0.37 0.010 1.000 1 2008 2008
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: rs7001819
rs7001819
LOC105379243
4 0.925 0.080 8 11792966 upstream gene variant T/C snv 0.35 0.010 < 0.001 1 2009 2009