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: rs11904814
rs11904814
CREB1
5 0.851 0.080 2 207562074 intron variant T/G snv 0.30 0.010 1.000 1 2010 2010
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: rs120074175
rs120074175
TPH2
7 0.827 0.080 12 72031544 missense variant G/A snv 1.2E-05 7.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs12137417
rs12137417
DISC1 ; TSNAX-DISC1
3 0.925 0.080 1 231950407 intron variant G/A snv 0.17 0.010 1.000 1 2011 2011
dbSNP: rs12229394
rs12229394
TPH2
3 0.925 0.080 12 71999134 intron variant G/A snv 0.29 0.010 1.000 1 2010 2010
dbSNP: rs12630592
rs12630592
GSK3B
5 0.851 0.080 3 120049399 intron variant G/A;T snv 0.010 1.000 1 2017 2017
dbSNP: rs12936511
rs12936511
CRHR1 ; MAPT-AS1 ; LINC02210-CRHR1
5 0.925 0.080 17 45807036 synonymous variant C/T snv 3.1E-02 3.0E-02 0.010 1.000 1 2009 2009
dbSNP: rs13440581
rs13440581
GPR50
5 0.882 0.080 X 151181399 missense variant A/G snv 0.45 0.45 0.010 1.000 1 2015 2015
dbSNP: rs1364647619
rs1364647619
POMC
3 0.925 0.080 2 25161334 missense variant C/T snv 0.010 1.000 1 2011 2011
dbSNP: rs139315125
rs139315125
PER3
7 0.851 0.080 1 7809900 missense variant A/G snv 5.6E-03 5.0E-03 0.010 1.000 1 2016 2016
dbSNP: rs139832701
rs139832701
CAV3
3 0.925 0.080 3 8773124 intron variant T/G snv 0.13 0.010 1.000 1 2014 2014
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: rs1409851868
rs1409851868
EPHA3
6 0.882 0.080 3 89399325 missense variant A/G snv 0.010 1.000 1 2019 2019
dbSNP: rs1415259
rs1415259
NOS1AP ; LOC105371475
5 0.925 0.080 1 162115519 intron variant C/T snv 0.54 0.010 1.000 1 2015 2015
dbSNP: rs1488864
rs1488864
CAVIN3 ; LOC101927825
4 0.851 0.080 11 6321099 intron variant T/G snv 0.80 0.010 1.000 1 2017 2017
dbSNP: rs1491850
rs1491850 		6 0.925 0.080 11 27728178 intron variant T/C snv 0.37 0.010 1.000 1 2011 2011
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: rs156243
rs156243 		6 0.925 0.080 6 104416939 intergenic variant G/A snv 0.65 0.010 1.000 1 2014 2014
dbSNP: rs174696
rs174696
COMT
3 0.925 0.080 22 19965653 intron variant C/A;T snv 0.010 1.000 1 2019 2019
dbSNP: rs174697
rs174697
ARVCF ; COMT
5 0.851 0.080 22 19966309 intron variant A/G snv 0.88 0.010 1.000 1 2012 2012
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: rs1799913
rs1799913
TPH1
5 0.851 0.080 11 18025708 splice region variant G/A;T snv 0.39 0.33 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: rs1858232
rs1858232
NOS1AP
4 0.882 0.080 1 162334048 intron variant A/G;T snv 0.010 1.000 1 2015 2015
dbSNP: rs1937863
rs1937863
AKR1C2
3 0.925 0.080 10 5009340 intron variant G/A;C;T snv 0.010 1.000 1 2017 2017