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: 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: 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
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: rs5743708
rs5743708
TLR2
97 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 0.010 1.000 1 2016 2016
dbSNP: rs6013029
rs6013029
CTNNBL1
2 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: rs6265
rs6265
BDNF ; BDNF-AS
264 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.010 1.000 1 2019 2019
dbSNP: rs6449213
rs6449213
SLC2A9 ; LOC105374476
3 0.827 0.240 4 9992591 intron variant C/T snv 0.82 0.010 1.000 1 2008 2008
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: rs7001819
rs7001819
LOC105379243
2 0.925 0.080 8 11792966 upstream gene variant T/C snv 0.35 0.010 < 0.001 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: rs750845408
rs750845408
PCSK1 ; LOC101929710
2 0.925 0.080 5 96423317 missense variant T/C snv 4.5E-05 7.0E-05 0.010 1.000 1 2015 2015
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: rs757139012
rs757139012
SIM1
3 0.882 0.080 6 100390522 missense variant T/C snv 8.0E-06; 4.0E-06 1.4E-05 0.010 1.000 1 2013 2013
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: 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: rs917346005
rs917346005
CADM2
2 0.925 0.080 3 85912502 missense variant A/G snv 0.010 1.000 1 2015 2015
dbSNP: rs943003
rs943003
ENPP1
3 0.882 0.120 6 131819872 non coding transcript exon variant C/T snv 0.64 0.010 1.000 1 2008 2008
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: 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
80 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2012 2012