rs796052798

Orientation

minus

Stabilized

minus

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

Make rs796052798(C;C)

Make rs796052798(C;G)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

100408174

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs796052798
dbSNP (classic)	rs796052798
ClinGen	rs796052798
ebi	rs796052798
HLI	rs796052798
Exac	rs796052798
Gnomad	rs796052798
Varsome	rs796052798
LitVar	rs796052798
Map	rs796052798
PheGenI	rs796052798
Biobank	rs796052798
1000 genomes	rs796052798
hgdp	rs796052798
ensembl	rs796052798
geneview	rs796052798
scholar	rs796052798
google	rs796052798
pharmgkb	rs796052798
gwascentral	rs796052798
openSNP	rs796052798
23andMe	rs796052798
SNPshot	rs796052798
SNPdbe	rs796052798
MSV3d	rs796052798
GWAS Ctlg	rs796052798

Max Magnitude

0

ClinVar
Risk	rs796052798(C;C)
Alt	rs796052798(C;C)
Reference	Rs796052798(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PCDH19
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.99663172C>G
CLNSRC
CLNACC	RCV000188348.1,