rs796052797

Orientation

minus

Stabilized

minus

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

Make rs796052797(G;T)

Make rs796052797(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

100408228

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs796052797
dbSNP (classic)	rs796052797
ClinGen	rs796052797
ebi	rs796052797
HLI	rs796052797
Exac	rs796052797
Gnomad	rs796052797
Varsome	rs796052797
LitVar	rs796052797
Map	rs796052797
PheGenI	rs796052797
Biobank	rs796052797
1000 genomes	rs796052797
hgdp	rs796052797
ensembl	rs796052797
geneview	rs796052797
scholar	rs796052797
google	rs796052797
pharmgkb	rs796052797
gwascentral	rs796052797
openSNP	rs796052797
23andMe	rs796052797
SNPshot	rs796052797
SNPdbe	rs796052797
MSV3d	rs796052797
GWAS Ctlg	rs796052797

Max Magnitude

0

ClinVar
Risk	rs796052797(T;T)
Alt	rs796052797(T;T)
Reference	Rs796052797(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PCDH19
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.99663226C>A
CLNSRC
CLNACC	RCV000188347.2,