rs796052811

Orientation

minus

Stabilized

minus

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

Make rs796052811(C;T)

Make rs796052811(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

100407567

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs796052811
dbSNP (classic)	rs796052811
ClinGen	rs796052811
ebi	rs796052811
HLI	rs796052811
Exac	rs796052811
Gnomad	rs796052811
Varsome	rs796052811
LitVar	rs796052811
Map	rs796052811
PheGenI	rs796052811
Biobank	rs796052811
1000 genomes	rs796052811
hgdp	rs796052811
ensembl	rs796052811
geneview	rs796052811
scholar	rs796052811
google	rs796052811
pharmgkb	rs796052811
gwascentral	rs796052811
openSNP	rs796052811
23andMe	rs796052811
SNPshot	rs796052811
SNPdbe	rs796052811
MSV3d	rs796052811
GWAS Ctlg	rs796052811

Max Magnitude

0

ClinVar
Risk	rs796052811(T;T)
Alt	rs796052811(T;T)
Reference	Rs796052811(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PCDH19
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.99662565G>A
CLNSRC
CLNACC	RCV000188363.1,