rs796052800

Orientation

minus

Stabilized

minus

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

Make rs796052800(A;A)

Make rs796052800(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

100408135

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs796052800
dbSNP (classic)	rs796052800
ClinGen	rs796052800
ebi	rs796052800
HLI	rs796052800
Exac	rs796052800
Gnomad	rs796052800
Varsome	rs796052800
LitVar	rs796052800
Map	rs796052800
PheGenI	rs796052800
Biobank	rs796052800
1000 genomes	rs796052800
hgdp	rs796052800
ensembl	rs796052800
geneview	rs796052800
scholar	rs796052800
google	rs796052800
pharmgkb	rs796052800
gwascentral	rs796052800
openSNP	rs796052800
23andMe	rs796052800
SNPshot	rs796052800
SNPdbe	rs796052800
MSV3d	rs796052800
GWAS Ctlg	rs796052800

Max Magnitude

0

ClinVar
Risk	rs796052800(A;A)
Alt	rs796052800(A;A)
Reference	Rs796052800(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PCDH19
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.99663133C>T
CLNSRC
CLNACC	RCV000188350.1,