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: rs1080963
rs1080963 		1 22 15376497 intergenic variant C/T snv 0.010 1.000 1 2018 2018
dbSNP: rs112025902
rs112025902 		4 0.925 0.080 4 120232669 intron variant A/G;T snv 0.010 1.000 1 2016 2016
dbSNP: rs11265263
rs11265263 		2 1 159740727 intergenic variant C/A;T snv 0.010 1.000 1 2018 2018
dbSNP: rs138191010
rs138191010 		1 7 145416641 intergenic variant G/T snv 0.010 < 0.001 1 2017 2017
dbSNP: rs1475157
rs1475157 		1 6 6016936 intergenic variant A/G snv 0.17 0.010 1.000 1 2017 2017
dbSNP: rs7582472
rs7582472 		1 2 133887223 regulatory region variant T/C snv 0.21 0.010 1.000 1 2012 2012
dbSNP: rs1045642
rs1045642
ABCB1
214 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2015 2015
dbSNP: rs1202184
rs1202184
ABCB1
7 0.851 0.120 7 87584585 intron variant C/T snv 0.39 0.010 1.000 1 2011 2011
dbSNP: rs1922242
rs1922242
ABCB1
8 0.827 0.120 7 87544351 intron variant A/T snv 0.43 0.010 1.000 1 2011 2011
dbSNP: rs11046205
rs11046205
ABCC9
2 12 21839392 intron variant G/A snv 0.19 0.010 1.000 1 2013 2013
dbSNP: rs776943620
rs776943620
ACE
7 0.851 0.120 17 63477287 missense variant G/A snv 2.1E-05 0.010 1.000 1 2009 2009
dbSNP: rs699
rs699
AGT
134 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.010 1.000 1 2008 2008
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 2007 2007
dbSNP: rs165599
rs165599
ARVCF ; COMT
27 0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 0.010 1.000 1 2010 2010
dbSNP: rs749437638
rs749437638
ARVCF ; COMT
14 0.752 0.240 22 19968597 missense variant C/T snv 2.4E-05 1.4E-05 0.010 1.000 1 2016 2016
dbSNP: rs6265
rs6265
BDNF ; BDNF-AS
272 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.100 0.967 30 2007 2020
dbSNP: rs759834365
rs759834365
BDNF ; BDNF-AS
237 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 0.100 0.964 28 2007 2020
dbSNP: rs7103411
rs7103411
BDNF ; BDNF-AS
15 0.752 0.160 11 27678578 intron variant C/T snv 0.82 0.010 1.000 1 2012 2012
dbSNP: rs7124442
rs7124442
BDNF ; BDNF-AS
9 0.827 0.160 11 27655494 3 prime UTR variant C/G;T snv 0.010 1.000 1 2012 2012
dbSNP: rs53576
rs53576
CAV3 ; OXTR
42 0.641 0.320 3 8762685 intron variant A/G;T snv 0.020 1.000 2 2019 2020
dbSNP: rs2254298
rs2254298
CAV3 ; OXTR
23 0.701 0.200 3 8760542 intron variant G/A snv 0.16 0.010 1.000 1 2011 2011
dbSNP: rs680244
rs680244
CHRNA5
4 0.882 0.120 15 78578946 intron variant T/C snv 0.60 0.010 1.000 1 2015 2015
dbSNP: rs11932595
rs11932595
CLOCK
12 0.827 0.160 4 55457430 intron variant A/G;T snv 0.010 1.000 1 2014 2014
dbSNP: rs1220000453
rs1220000453
CNTF ; ZFP91-CNTF
5 0.882 0.120 11 58624189 synonymous variant C/T snv 0.010 < 0.001 1 2006 2006
dbSNP: rs165774
rs165774
COMT
11 0.807 0.120 22 19965038 3 prime UTR variant G/A snv 0.27 0.010 < 0.001 1 2016 2016