rs132630325

Orientation

minus

Stabilized

minus

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

Make rs132630325(C;G)

Make rs132630325(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

100406586

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs132630325
dbSNP (classic)	rs132630325
ClinGen	rs132630325
ebi	rs132630325
HLI	rs132630325
Exac	rs132630325
Gnomad	rs132630325
Varsome	rs132630325
LitVar	rs132630325
Map	rs132630325
PheGenI	rs132630325
Biobank	rs132630325
1000 genomes	rs132630325
hgdp	rs132630325
ensembl	rs132630325
geneview	rs132630325
scholar	rs132630325
google	rs132630325
pharmgkb	rs132630325
gwascentral	rs132630325
openSNP	rs132630325
23andMe	rs132630325
SNPshot	rs132630325
SNPdbe	rs132630325
MSV3d	rs132630325
GWAS Ctlg	rs132630325

Max Magnitude

0

OMIM	300460
Desc
Variant	0004
Related	also

ClinVar
Risk	rs132630325(G;G)
Alt	rs132630325(G;G)
Reference	Rs132630325(C;C)
Significance	Pathogenic
Disease	Early infantile epileptic encephalopathy 9
Variation	info
Gene	PCDH19
CLNDBN	Early infantile epileptic encephalopathy 9
Reversed	1
HGVS	NC_000023.10:g.99661584G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000011765.7,