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: rs11264126
rs11264126
DLGAP3
1 1.000 0.120 1 34876494 intron variant G/A snv 0.41 0.010 1.000 1 2011 2011
dbSNP: rs12141243
rs12141243
DLGAP3
1 1.000 0.120 1 34881321 intron variant T/C snv 9.7E-02 0.010 1.000 1 2011 2011
dbSNP: rs1805404
rs1805404
PARP1
3 0.882 0.200 1 226402257 missense variant G/A;C snv 0.22; 4.0E-06 0.010 1.000 1 2013 2013
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: rs2708146
rs2708146
LINC01122
1 1.000 0.120 2 58728818 intron variant A/G snv 0.47 0.710 1.000 2 2019 2019
dbSNP: rs61752115
rs61752115
PEX13
7 0.807 0.320 2 61048535 missense variant T/C snv 4.0E-06 0.020 1.000 2 1999 2005
dbSNP: rs1013940
rs1013940
SLC5A7
6 0.827 0.160 2 107992192 missense variant A/G snv 9.3E-02 7.4E-02 0.010 1.000 1 2017 2017
dbSNP: rs13407215
rs13407215 		1 1.000 0.120 2 160688380 intergenic variant C/T snv 4.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs17561
rs17561
IL1A
23 0.672 0.560 2 112779646 missense variant C/A snv 0.27 0.26 0.010 < 0.001 1 2015 2015
dbSNP: rs1922786
rs1922786
LINC01122
1 1.000 0.120 2 58636438 intron variant A/G snv 0.29 0.010 1.000 1 2019 2019
dbSNP: rs2433718
rs2433718
SLC5A7
1 1.000 0.120 2 107986975 intron variant A/G snv 0.82 0.010 1.000 1 2017 2017
dbSNP: rs315952
rs315952
IL1RN
10 0.763 0.400 2 113132727 missense variant T/A;C snv 4.0E-06; 0.31 0.010 < 0.001 1 2015 2015
dbSNP: rs4676169
rs4676169
SLC5A7
1 1.000 0.120 2 107993689 intron variant A/G snv 0.46 0.010 1.000 1 2017 2017
dbSNP: rs4988462
rs4988462
POU1F1
2 0.925 0.120 3 87264203 intron variant C/T snv 0.31 0.700 1.000 1 2015 2015
dbSNP: rs6280
rs6280
DRD3
57 0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 0.010 < 0.001 1 2015 2015
dbSNP: rs4047771
rs4047771
LOC285500
1 1.000 0.120 4 177549744 intron variant A/C snv 0.28 0.700 1.000 1 2019 2019
dbSNP: rs1800044
rs1800044
HTR1A
8 0.827 0.200 5 63961061 missense variant C/A snv 3.7E-03 3.8E-03 0.010 1.000 1 1996 1996
dbSNP: rs2032892
rs2032892
SLC1A3
1 1.000 0.120 5 36676981 missense variant G/C snv 2.5E-02 1.9E-02 0.010 1.000 1 2011 2011
dbSNP: rs9357271
rs9357271
BTBD9
8 0.776 0.160 6 38398097 intron variant T/C snv 0.38 0.030 1.000 3 2009 2014
dbSNP: rs9296249
rs9296249
BTBD9
3 0.882 0.120 6 38398065 intron variant T/C snv 0.30 0.020 1.000 2 2012 2014
dbSNP: rs1049353
rs1049353
CNR1
42 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 0.010 1.000 1 2004 2004
dbSNP: rs1800629
rs1800629
TNF
169 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2014 2014
dbSNP: rs1906252
rs1906252 		3 0.925 0.120 6 98102413 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs361525
rs361525
TNF
62 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.010 1.000 1 2014 2014
dbSNP: rs4714156
rs4714156
BTBD9
2 0.925 0.120 6 38393336 intron variant C/T snv 0.36 0.010 1.000 1 2014 2014