rs794726897

Orientation

minus

Stabilized

minus

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

Make rs794726897(C;T)

Make rs794726897(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

100407784

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs794726897
dbSNP (classic)	rs794726897
ClinGen	rs794726897
ebi	rs794726897
HLI	rs794726897
Exac	rs794726897
Gnomad	rs794726897
Varsome	rs794726897
LitVar	rs794726897
Map	rs794726897
PheGenI	rs794726897
Biobank	rs794726897
1000 genomes	rs794726897
hgdp	rs794726897
ensembl	rs794726897
geneview	rs794726897
scholar	rs794726897
google	rs794726897
pharmgkb	rs794726897
gwascentral	rs794726897
openSNP	rs794726897
23andMe	rs794726897
SNPshot	rs794726897
SNPdbe	rs794726897
MSV3d	rs794726897
GWAS Ctlg	rs794726897

Max Magnitude

0

ClinVar
Risk	rs794726897(T;T)
Alt	rs794726897(T;T)
Reference	Rs794726897(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.99662782G>A
CLNSRC
CLNACC	RCV000173238.1,