rs796052812

Orientation

minus

Stabilized

minus

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

Make rs796052812(C;T)

Make rs796052812(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

100407484

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs796052812
dbSNP (classic)	rs796052812
ClinGen	rs796052812
ebi	rs796052812
HLI	rs796052812
Exac	rs796052812
Gnomad	rs796052812
Varsome	rs796052812
LitVar	rs796052812
Map	rs796052812
PheGenI	rs796052812
Biobank	rs796052812
1000 genomes	rs796052812
hgdp	rs796052812
ensembl	rs796052812
geneview	rs796052812
scholar	rs796052812
google	rs796052812
pharmgkb	rs796052812
gwascentral	rs796052812
openSNP	rs796052812
23andMe	rs796052812
SNPshot	rs796052812
SNPdbe	rs796052812
MSV3d	rs796052812
GWAS Ctlg	rs796052812

Max Magnitude

0

ClinVar
Risk	rs796052812(T;T)
Alt	rs796052812(T;T)
Reference	Rs796052812(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PCDH19
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.99662482G>A
CLNSRC
CLNACC	RCV000188364.1,