rs587784300

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs587784300(G;T)

Make rs587784300(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

100407808

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs587784300
dbSNP (classic)	rs587784300
ClinGen	rs587784300
ebi	rs587784300
HLI	rs587784300
Exac	rs587784300
Gnomad	rs587784300
Varsome	rs587784300
LitVar	rs587784300
Map	rs587784300
PheGenI	rs587784300
Biobank	rs587784300
1000 genomes	rs587784300
hgdp	rs587784300
ensembl	rs587784300
geneview	rs587784300
scholar	rs587784300
google	rs587784300
pharmgkb	rs587784300
gwascentral	rs587784300
openSNP	rs587784300
23andMe	rs587784300
SNPshot	rs587784300
SNPdbe	rs587784300
MSV3d	rs587784300
GWAS Ctlg	rs587784300

Max Magnitude

0

ClinVar
Risk	rs587784300(T;T)
Alt	rs587784300(T;T)
Reference	Rs587784300(G;G)
Significance	Probable-Pathogenic
Disease	Early infantile epileptic encephalopathy 9 not provided
Variation	info
Gene	PCDH19
CLNDBN	Early infantile epileptic encephalopathy 9 not provided
Reversed	1
HGVS	NC_000023.10:g.99662806C>A
CLNSRC
CLNACC	RCV000147085.1, RCV000490161.1,