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: rs4722404
rs4722404 		4 0.851 0.120 7 3089155 intron variant T/C snv 0.40 0.020 1.000 2 2016 2017
dbSNP: rs4845454
rs4845454 		2 0.925 0.040 1 152619708 downstream gene variant C/A;T snv 0.710 1.000 2 2015 2018
dbSNP: rs6887695
rs6887695 		14 0.732 0.440 5 159395637 intron variant G/C snv 0.35 0.020 1.000 2 2009 2013
dbSNP: rs1010824
rs1010824 		1 1.000 0.040 8 107239685 intergenic variant G/A snv 0.14 0.010 1.000 1 2015 2015
dbSNP: rs10733113
rs10733113 		3 0.882 0.160 1 247459055 upstream gene variant A/G snv 0.81 0.010 1.000 1 2018 2018
dbSNP: rs10865331
rs10865331 		5 0.827 0.120 2 62324337 intergenic variant A/G snv 0.57 0.700 1.000 1 2015 2015
dbSNP: rs12884468
rs12884468 		2 0.925 0.040 14 35383280 downstream gene variant T/C snv 0.47 0.700 1.000 1 2015 2015
dbSNP: rs17728338
rs17728338 		4 0.851 0.160 5 151098757 downstream gene variant G/A snv 7.1E-02 0.010 1.000 1 2013 2013
dbSNP: rs2675669
rs2675669 		1 1.000 0.040 10 73894114 intergenic variant C/T snv 0.55 0.700 1.000 1 2015 2015
dbSNP: rs4649203
rs4649203 		4 0.851 0.160 1 24193430 intergenic variant G/A snv 0.61 0.010 1.000 1 2013 2013
dbSNP: rs4683946
rs4683946 		2 0.925 0.080 3 101896982 intron variant G/T snv 0.19 0.700 1.000 1 2015 2015
dbSNP: rs4810482
rs4810482 		1 1.000 0.040 20 46005911 upstream gene variant T/C snv 0.45 0.010 1.000 1 2015 2015
dbSNP: rs6474412
rs6474412 		4 0.925 0.120 8 42695355 upstream gene variant C/T snv 0.64 0.010 1.000 1 2014 2014
dbSNP: rs7552167
rs7552167 		6 0.807 0.120 1 24192153 upstream gene variant A/G snv 0.87 0.700 1.000 1 2015 2015
dbSNP: rs878329
rs878329 		4 0.882 0.120 17 5649930 intergenic variant G/C snv 0.44 0.010 1.000 1 2018 2018
dbSNP: rs1868554
rs1868554
ANGPT2 ; MCPH1
1 1.000 0.040 8 6529226 intron variant T/A;C;G snv 0.010 1.000 1 2015 2015
dbSNP: rs2442598
rs2442598
ANGPT2 ; MCPH1
2 0.925 0.120 8 6537300 intron variant T/C snv 0.71 0.010 1.000 1 2015 2015
dbSNP: rs3739390
rs3739390
ANGPT2 ; MCPH1
1 1.000 0.040 8 6562969 5 prime UTR variant C/G snv 6.7E-02 5.9E-02 0.010 1.000 1 2015 2015
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 2014 2014
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 2014 2014
dbSNP: rs12489120
rs12489120
BHLHE40 ; BHLHE40-AS1
1 1.000 0.040 3 4978778 intron variant C/A;G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs2675662
rs2675662
CAMK2G
2 0.925 0.040 10 73839369 intron variant A/G snv 0.55 0.700 1.000 1 2015 2015
dbSNP: rs201285077
rs201285077
CARD14
3 0.882 0.040 17 80198545 missense variant C/G;T snv 4.0E-06; 2.3E-04 3.1E-04 0.010 1.000 1 2016 2016
dbSNP: rs518604
rs518604
CASP5
1 1.000 0.040 11 104998504 intron variant G/A snv 0.58 0.010 1.000 1 2015 2015
dbSNP: rs523104
rs523104
CASP5
1 1.000 0.040 11 104998981 missense variant G/C;T snv 0.46; 4.0E-06 0.010 1.000 1 2015 2015