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: rs796052839
rs796052839
PCDH19
3 0.882 0.200 X 100407579 missense variant T/C;G snv 0.800 1.000 17 1990 2017
dbSNP: rs587784299
rs587784299
PCDH19
1 1.000 0.200 X 100407903 missense variant T/A;C snv 0.800 1.000 15 2008 2017
dbSNP: rs1555985448
rs1555985448
PCDH19
1 1.000 0.200 X 100407813 missense variant G/T snv 0.700 1.000 12 2008 2016
dbSNP: rs1555985475
rs1555985475
PCDH19
1 1.000 0.200 X 100407897 missense variant T/C snv 0.700 1.000 12 2008 2016
dbSNP: rs201989363
rs201989363
PCDH19
1 1.000 0.200 X 100406898 missense variant G/A;C;T snv 4.4E-05 0.800 1.000 12 2008 2016
dbSNP: rs267606933
rs267606933
PCDH19
1 1.000 0.200 X 100406927 missense variant G/A;C snv 0.800 1.000 12 2008 2016
dbSNP: rs753757730
rs753757730
PCDH19
1 1.000 0.200 X 100408027 missense variant C/G;T snv 5.6E-06; 5.6E-06 0.700 1.000 12 2008 2016
dbSNP: rs1569315231
rs1569315231
PCDH19
1 1.000 0.200 X 100407680 stop gained G/C snv 0.700 1.000 1 2016 2016
dbSNP: rs769967221
rs769967221
PCDH19
1 1.000 0.200 X 100407415 stop gained G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1057521256
rs1057521256
PCDH19
1 1.000 0.200 X 100406783 stop gained G/A;C snv 0.700 0
dbSNP: rs1060502176
rs1060502176
PCDH19
1 1.000 0.200 X 100407891 missense variant G/A;C snv 0.700 0
dbSNP: rs132630323
rs132630323
PCDH19
1 1.000 0.200 X 100407276 missense variant A/T snv 0.800 0
dbSNP: rs132630324
rs132630324
PCDH19
1 1.000 0.200 X 100408345 stop gained G/A snv 0.700 0
dbSNP: rs132630325
rs132630325
PCDH19
1 1.000 0.200 X 100406586 stop gained G/C snv 0.700 0
dbSNP: rs132630326
rs132630326
PCDH19
1 1.000 0.200 X 100408456 stop gained C/A;T snv 0.700 0
dbSNP: rs1555985105
rs1555985105
PCDH19
1 1.000 0.200 X 100407043 stop gained G/A snv 0.700 0
dbSNP: rs1555985780
rs1555985780
PCDH19
1 1.000 0.200 X 100408330 missense variant C/G snv 0.700 0
dbSNP: rs1569314809
rs1569314809
PCDH19
1 1.000 0.200 X 100407256 missense variant C/A snv 0.700 0
dbSNP: rs1569315876
rs1569315876
PCDH19
1 1.000 0.200 X 100408136 stop gained G/C snv 0.700 0
dbSNP: rs746274631
rs746274631
PCDH19
1 1.000 0.200 X 100407981 missense variant A/C snv 1.1E-05 5.6E-05 0.700 0
dbSNP: rs796052795
rs796052795
PCDH19
1 1.000 0.200 X 100408237 missense variant C/G;T snv 0.700 0
dbSNP: rs796052799
rs796052799
PCDH19
1 1.000 0.200 X 100408161 missense variant G/C snv 0.700 0
dbSNP: rs796052812
rs796052812
PCDH19
1 1.000 0.200 X 100407484 missense variant G/A snv 0.700 0
dbSNP: rs796052819
rs796052819
PCDH19
1 1.000 0.200 X 100406916 missense variant G/C snv 0.700 0
dbSNP: rs796052837
rs796052837
PCDH19
1 1.000 0.200 X 100408100 stop gained G/C;T snv 0.700 0