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: rs10997875
rs10997875 		4 0.882 0.080 10 67920067 downstream gene variant T/A;C snv 0.010 1.000 1 2019 2019
dbSNP: rs112025902
rs112025902 		4 0.925 0.080 4 120232669 intron variant A/G;T snv 0.010 1.000 1 2016 2016
dbSNP: rs115482041
rs115482041
RCL1
4 0.925 0.080 9 4860267 missense variant C/T snv 2.6E-03 2.3E-03 0.010 1.000 1 2018 2018
dbSNP: rs11636753
rs11636753
CHRNB4
4 0.882 0.120 15 78636604 intron variant G/T snv 0.35 0.010 1.000 1 2012 2012
dbSNP: rs11911834
rs11911834
S100B
4 0.882 0.080 21 46602608 5 prime UTR variant G/A;T snv 0.010 1.000 1 2009 2009
dbSNP: rs1402757753
rs1402757753
P2RX2
4 0.882 0.080 12 132621913 missense variant G/A snv 7.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs143830698
rs143830698
ACE
4 0.882 0.120 17 63488659 missense variant G/A snv 8.4E-05 0.010 1.000 1 2013 2013
dbSNP: rs1491851
rs1491851 		4 0.925 0.080 11 27731216 intron variant T/C;G snv 0.41 0.010 1.000 1 2011 2011
dbSNP: rs1743963
rs1743963
SGK1
4 0.882 0.120 6 134176537 intron variant G/A;C snv 0.010 1.000 1 2019 2019
dbSNP: rs1763509
rs1763509
SGK1
4 0.882 0.120 6 134233200 intron variant G/A;T snv 0.010 1.000 1 2019 2019
dbSNP: rs17759843
rs17759843
PPM1F
4 0.882 0.080 22 21920372 3 prime UTR variant G/A snv 6.7E-02 0.010 1.000 1 2018 2018
dbSNP: rs1800035
rs1800035
ADRA2A
4 0.925 0.080 10 111078794 missense variant C/G;T snv 1.9E-03 0.010 < 0.001 1 2006 2006
dbSNP: rs1800041
rs1800041
HTR1A
4 0.882 0.120 5 63961673 missense variant G/A snv 1.8E-03 5.3E-04 0.010 1.000 1 2004 2004
dbSNP: rs1858232
rs1858232
NOS1AP
4 0.882 0.080 1 162334048 intron variant A/G;T snv 0.010 1.000 1 2015 2015
dbSNP: rs1863918
rs1863918
ADAMTS2
4 0.882 0.160 5 179112381 3 prime UTR variant G/T snv 0.25 0.010 1.000 1 2016 2016
dbSNP: rs2228079
rs2228079
ADORA1
4 0.882 0.160 1 203129147 synonymous variant T/G snv 0.31 0.26 0.010 1.000 1 2015 2015
dbSNP: rs2910709
rs2910709
GDNF-AS1
4 0.882 0.120 5 37811762 non coding transcript exon variant A/G;T snv 0.010 1.000 1 2013 2013
dbSNP: rs3125
rs3125
HTR2A
4 0.925 0.080 13 46834716 3 prime UTR variant C/G;T snv 0.010 1.000 1 2019 2019
dbSNP: rs36010656
rs36010656
SLCO1C1
4 0.925 0.080 12 20711408 missense variant C/A;T snv 3.4E-02 0.010 1.000 1 2008 2008
dbSNP: rs371356064
rs371356064
P2RX7 ; LOC105370032
4 0.882 0.120 12 121133072 synonymous variant C/T snv 1.2E-05 7.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs386231
rs386231
NOS1AP
4 0.882 0.080 1 162356033 intron variant C/T snv 0.68 0.010 1.000 1 2013 2013
dbSNP: rs3916966
rs3916966 		4 0.882 0.080 13 105458546 upstream gene variant C/A snv 0.63 0.010 < 0.001 1 2010 2010
dbSNP: rs4305745
rs4305745 		4 0.882 0.080 6 132572573 downstream gene variant G/A snv 0.55 0.010 1.000 1 2010 2010
dbSNP: rs4672619
rs4672619
ERBB4
4 0.882 0.160 2 211592470 intron variant C/A;G snv 0.010 1.000 1 2018 2018
dbSNP: rs4792887
rs4792887
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
4 0.882 0.080 17 45799654 non coding transcript exon variant C/T snv 0.16 0.010 1.000 1 2009 2009