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: rs16859788
rs16859788
GABRA4
1 1.000 0.040 4 46969992 intron variant A/C;T snv 0.010 1.000 1 2006 2006
dbSNP: rs7741604
rs7741604
CDKAL1
2 0.925 0.120 6 20731293 intron variant A/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs971257
rs971257
B3GALT1
1 1.000 0.040 2 167782126 intergenic variant A/C;T snv 0.53 0.010 1.000 1 2008 2008
dbSNP: rs1217691063
rs1217691063
MTHFR
614 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.080 1.000 8 2009 2019
dbSNP: rs1801394
rs1801394
MTRR ; FASTKD3
101 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.020 1.000 2 2009 2016
dbSNP: rs1805087
rs1805087
MTR
135 0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 0.020 1.000 2 2009 2016
dbSNP: rs10500171
rs10500171
CNTNAP2
1 1.000 0.040 7 147183313 intron variant A/G snv 0.52 0.010 1.000 1 2010 2010
dbSNP: rs10732392
rs10732392
LMX1B
1 1.000 0.040 9 126633758 intron variant A/G snv 0.84 0.010 1.000 1 2011 2011
dbSNP: rs11102807
rs11102807 		1 1.000 0.040 1 114518963 intergenic variant A/G snv 0.44 0.800 1.000 1 2014 2014
dbSNP: rs11191454
rs11191454
AS3MT ; BORCS7-ASMT ; LOC107984265
9 0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 0.010 1.000 1 2019 2019
dbSNP: rs12336217
rs12336217
LMX1B
1 1.000 0.040 9 126637591 intron variant A/G snv 0.17 0.010 1.000 1 2011 2011
dbSNP: rs12456492
rs12456492
RIT2
3 0.882 0.080 18 43093415 intron variant A/G snv 0.33 0.010 1.000 1 2017 2017
dbSNP: rs12518194
rs12518194 		1 1.000 0.040 5 25951452 intergenic variant A/G snv 0.27 0.700 1.000 1 2009 2009
dbSNP: rs1408744
rs1408744 		1 1.000 0.040 6 23789887 intergenic variant A/G snv 0.63 0.700 1.000 1 2012 2012
dbSNP: rs1426217
rs1426217
GABRB3
1 1.000 0.040 15 26575978 intron variant A/G snv 0.46 0.010 < 0.001 1 2018 2018
dbSNP: rs155806
rs155806
PCDHA9 ; PCDHAC2 ; PCDHAC1 ; PCDHA13 ; PCDHA12 ; PCDHA11 ; PCDHA10 ; PCDHA8 ; PCDHA7 ; PCDHA6 ; PCDHA5 ; PCDHA4 ; PCDHA3 ; PCDHA2 ; PCDHA1
2 1.000 0.040 5 140970255 intron variant A/G snv 8.9E-02 0.010 1.000 1 2013 2013
dbSNP: rs17599416
rs17599416
GABRA4
1 1.000 0.040 4 46971421 intron variant A/G snv 0.13 0.010 1.000 1 2006 2006
dbSNP: rs1799971
rs1799971
OPRM1
95 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 0.010 1.000 1 2015 2015
dbSNP: rs2194079
rs2194079
MEGF10 ; LOC105379199
1 1.000 0.040 5 127292406 intron variant A/G snv 0.49 0.010 1.000 1 2017 2017
dbSNP: rs263030
rs263030
YEATS2 ; YEATS2-AS1
1 1.000 0.040 3 183807333 non coding transcript exon variant A/G snv 0.44 0.700 1.000 1 2012 2012
dbSNP: rs263035
rs263035
YEATS2
1 1.000 0.040 3 183805869 intron variant A/G snv 0.44 0.700 1.000 1 2012 2012
dbSNP: rs3746599
rs3746599
DUSP15
1 1.000 0.040 20 31849719 intron variant A/G snv 0.44 0.55 0.010 1.000 1 2017 2017
dbSNP: rs38841
rs38841
MET
1 1.000 0.040 7 116679872 intron variant A/G snv 0.28 0.010 1.000 1 2010 2010
dbSNP: rs409649
rs409649 		1 1.000 0.040 5 25841054 intergenic variant A/G snv 0.29 0.700 1.000 1 2009 2009
dbSNP: rs4701259
rs4701259 		1 1.000 0.040 5 25900989 intergenic variant A/G snv 0.71 0.700 1.000 1 2009 2009