rs796052806

Orientation

minus

Stabilized

minus

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

Make rs796052806(C;C)

Make rs796052806(C;G)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

100407964

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs796052806
dbSNP (classic)	rs796052806
ClinGen	rs796052806
ebi	rs796052806
HLI	rs796052806
Exac	rs796052806
Gnomad	rs796052806
Varsome	rs796052806
LitVar	rs796052806
Map	rs796052806
PheGenI	rs796052806
Biobank	rs796052806
1000 genomes	rs796052806
hgdp	rs796052806
ensembl	rs796052806
geneview	rs796052806
scholar	rs796052806
google	rs796052806
pharmgkb	rs796052806
gwascentral	rs796052806
openSNP	rs796052806
23andMe	rs796052806
SNPshot	rs796052806
SNPdbe	rs796052806
MSV3d	rs796052806
GWAS Ctlg	rs796052806

Max Magnitude

0

ClinVar
Risk	rs796052806(C;C)
Alt	rs796052806(C;C)
Reference	Rs796052806(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PCDH19
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.99662962C>G
CLNSRC
CLNACC	RCV000188356.2,