rs796052822

Orientation

minus

Stabilized

minus

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

Make rs796052822(A;G)

Make rs796052822(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

100406725

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs796052822
dbSNP (classic)	rs796052822
ClinGen	rs796052822
ebi	rs796052822
HLI	rs796052822
Exac	rs796052822
Gnomad	rs796052822
Varsome	rs796052822
LitVar	rs796052822
Map	rs796052822
PheGenI	rs796052822
Biobank	rs796052822
1000 genomes	rs796052822
hgdp	rs796052822
ensembl	rs796052822
geneview	rs796052822
scholar	rs796052822
google	rs796052822
pharmgkb	rs796052822
gwascentral	rs796052822
openSNP	rs796052822
23andMe	rs796052822
SNPshot	rs796052822
SNPdbe	rs796052822
MSV3d	rs796052822
GWAS Ctlg	rs796052822

Max Magnitude

0

ClinVar
Risk	rs796052822(G;G)
Alt	rs796052822(G;G)
Reference	Rs796052822(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PCDH19
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.99661723T>C
CLNSRC
CLNACC	RCV000188377.2,