rs796052817

Orientation

minus

Stabilized

minus

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

Make rs796052817(C;G)

Make rs796052817(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

100406973

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs796052817
dbSNP (classic)	rs796052817
ClinGen	rs796052817
ebi	rs796052817
HLI	rs796052817
Exac	rs796052817
Gnomad	rs796052817
Varsome	rs796052817
LitVar	rs796052817
Map	rs796052817
PheGenI	rs796052817
Biobank	rs796052817
1000 genomes	rs796052817
hgdp	rs796052817
ensembl	rs796052817
geneview	rs796052817
scholar	rs796052817
google	rs796052817
pharmgkb	rs796052817
gwascentral	rs796052817
openSNP	rs796052817
23andMe	rs796052817
SNPshot	rs796052817
SNPdbe	rs796052817
MSV3d	rs796052817
GWAS Ctlg	rs796052817

Max Magnitude

0

ClinVar
Risk	rs796052817(G;G)
Alt	rs796052817(G;G)
Reference	Rs796052817(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PCDH19
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.99661971G>C
CLNSRC
CLNACC	RCV000188372.1,