rs796052813

Orientation

minus

Stabilized

minus

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

Make rs796052813(G;T)

Make rs796052813(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

100407358

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs796052813
dbSNP (classic)	rs796052813
ClinGen	rs796052813
ebi	rs796052813
HLI	rs796052813
Exac	rs796052813
Gnomad	rs796052813
Varsome	rs796052813
LitVar	rs796052813
Map	rs796052813
PheGenI	rs796052813
Biobank	rs796052813
1000 genomes	rs796052813
hgdp	rs796052813
ensembl	rs796052813
geneview	rs796052813
scholar	rs796052813
google	rs796052813
pharmgkb	rs796052813
gwascentral	rs796052813
openSNP	rs796052813
23andMe	rs796052813
SNPshot	rs796052813
SNPdbe	rs796052813
MSV3d	rs796052813
GWAS Ctlg	rs796052813

Max Magnitude

0

ClinVar
Risk	rs796052813(T;T)
Alt	rs796052813(T;T)
Reference	Rs796052813(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PCDH19
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.99662356C>A
CLNSRC
CLNACC	RCV000188366.1,