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: rs1356639869
rs1356639869
NPY ; LOC107986777
2 1.000 0.040 7 24289527 missense variant C/A snv 0.010 1.000 1 2011 2011
dbSNP: rs16139
rs16139
NPY ; LOC107986777
36 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 0.010 1.000 1 2011 2011
dbSNP: rs74566133
rs74566133 		2 8 133766099 regulatory region variant C/T snv 2.6E-02 0.700 1.000 1 2013 2013
dbSNP: rs6265
rs6265
BDNF ; BDNF-AS
272 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.080 0.750 8 2004 2019
dbSNP: rs759834365
rs759834365
BDNF ; BDNF-AS
237 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 0.070 0.714 7 2004 2016
dbSNP: rs746682028
rs746682028
BDNF ; BDNF-AS
36 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 0.020 0.500 2 2004 2010
dbSNP: rs1800497
rs1800497
ANKK1
56 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 0.010 1.000 1 2012 2012
dbSNP: rs1473473
rs1473473
TPH2
4 0.925 0.080 12 72010598 intron variant C/A;T snv 0.81 0.020 1.000 2 2011 2013
dbSNP: rs10858583
rs10858583
LOC107984478
3 1.000 0.040 12 87334666 intergenic variant C/T snv 0.79 0.700 1.000 1 2016 2016
dbSNP: rs6311
rs6311
HTR2A
41 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.010 1.000 1 2019 2019
dbSNP: rs6313
rs6313
HTR2A
82 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 0.010 1.000 1 2019 2019
dbSNP: rs7322916
rs7322916
ATP8A2
2 13 25433839 intron variant G/A;C snv 0.800 1.000 1 2013 2013
dbSNP: rs7180942
rs7180942
NTRK3
1 15 88131345 intron variant T/C snv 0.56 0.010 1.000 1 2008 2008
dbSNP: rs12149074
rs12149074
LOC105371357
3 1.000 0.040 16 80071969 intron variant C/A;G snv 0.700 1.000 1 2016 2016
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: rs4148087
rs4148087
ABCG1
3 1.000 0.040 21 42202157 intron variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs4680
rs4680
COMT ; MIR4761
249 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 0.030 0.667 3 2012 2018