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: rs104893877
rs104893877
SNCA
59 0.614 0.360 4 89828149 missense variant C/T snv 0.030 1.000 3 2013 2020
dbSNP: rs110402
rs110402
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
12 0.790 0.120 17 45802681 intron variant G/A;C snv 0.030 1.000 3 2013 2019
dbSNP: rs25531
rs25531
SLC6A4 ; LOC105371720
72 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 0.030 1.000 3 2011 2019
dbSNP: rs6295
rs6295
HTR1A
40 0.645 0.200 5 63962738 intron variant C/G snv 0.49 0.030 1.000 3 2010 2018
dbSNP: rs1709393
rs1709393
LINC02085
2 1.000 0.080 3 101980310 intron variant C/T snv 0.55 0.700 1.000 2 2016 2019
dbSNP: rs2180619
rs2180619
CNR1
3 1.000 0.040 6 88168233 upstream gene variant G/A snv 0.53 0.020 1.000 2 2009 2014
dbSNP: rs2254298
rs2254298
CAV3 ; OXTR
23 0.701 0.200 3 8760542 intron variant G/A snv 0.16 0.020 1.000 2 2011 2012
dbSNP: rs2298383
rs2298383
ADORA2A ; ADORA2A-AS1 ; SPECC1L-ADORA2A
11 0.827 0.200 22 24429543 non coding transcript exon variant C/A;T snv 0.020 1.000 2 2008 2019
dbSNP: rs3219151
rs3219151
GABRA6
14 0.752 0.160 5 161701908 3 prime UTR variant C/T snv 0.51 0.020 1.000 2 2017 2019
dbSNP: rs4570625
rs4570625
TPH2
25 0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 0.020 1.000 2 2013 2015
dbSNP: rs53576
rs53576
CAV3 ; OXTR
42 0.641 0.320 3 8762685 intron variant A/G;T snv 0.020 1.000 2 2016 2017
dbSNP: rs9470080
rs9470080
FKBP5
13 0.827 0.080 6 35678658 intron variant T/A;C snv 0.020 1.000 2 2012 2016
dbSNP: rs1006737
rs1006737
CACNA1C
27 0.695 0.120 12 2236129 intron variant G/A snv 0.36 0.010 1.000 1 2011 2011
dbSNP: rs10112596
rs10112596
GATA4
3 0.925 0.120 8 11722293 intron variant A/G snv 0.83 0.010 1.000 1 2018 2018
dbSNP: rs1012176
rs1012176
CTNND2
1 5 11320426 intron variant G/T snv 0.24 0.010 1.000 1 2014 2014
dbSNP: rs1043307
rs1043307
PSMD9
14 0.776 0.360 12 121915890 missense variant A/C;G snv 0.010 1.000 1 2015 2015
dbSNP: rs10801153
rs10801153 		3 0.925 0.080 1 192794818 intron variant G/A snv 0.27 0.010 1.000 1 2015 2015
dbSNP: rs10835210
rs10835210
BDNF ; BDNF-AS
4 0.882 0.040 11 27674363 intron variant C/A;G snv 0.010 1.000 1 2018 2018
dbSNP: rs10868235
rs10868235
NTRK2
6 0.925 0.040 9 84878840 intron variant C/T snv 0.40 0.010 1.000 1 2017 2017
dbSNP: rs10893268
rs10893268
OR8A1
1 11 124568716 intron variant C/T snv 0.40 0.700 1.000 1 2014 2014
dbSNP: rs11030107
rs11030107
BDNF ; BDNF-AS
2 1.000 0.040 11 27673288 intron variant A/G snv 0.19 0.010 1.000 1 2018 2018
dbSNP: rs11059336
rs11059336 		1 12 127745489 regulatory region variant T/C snv 0.14 0.700 1.000 1 2019 2019
dbSNP: rs1110976
rs1110976
DRD2
3 1.000 0.040 11 113413797 intron variant T/G snv 0.010 1.000 1 2008 2008
dbSNP: rs11111
rs11111
GDNF ; GDNF-AS1
5 0.882 0.080 5 37814000 3 prime UTR variant T/C snv 0.22 0.010 1.000 1 2013 2013
dbSNP: rs112146896
rs112146896
EFHD2
2 1.000 0.040 1 15418527 intron variant A/C;G;T snv 0.010 < 0.001 1 2018 2018