rs796052819

Orientation

minus

Stabilized

minus

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

Make rs796052819(C;G)

Make rs796052819(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

100406916

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs796052819
dbSNP (classic)	rs796052819
ClinGen	rs796052819
ebi	rs796052819
HLI	rs796052819
Exac	rs796052819
Gnomad	rs796052819
Varsome	rs796052819
LitVar	rs796052819
Map	rs796052819
PheGenI	rs796052819
Biobank	rs796052819
1000 genomes	rs796052819
hgdp	rs796052819
ensembl	rs796052819
geneview	rs796052819
scholar	rs796052819
google	rs796052819
pharmgkb	rs796052819
gwascentral	rs796052819
openSNP	rs796052819
23andMe	rs796052819
SNPshot	rs796052819
SNPdbe	rs796052819
MSV3d	rs796052819
GWAS Ctlg	rs796052819

Max Magnitude

0

ClinVar
Risk	rs796052819(G;G)
Alt	rs796052819(G;G)
Reference	Rs796052819(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PCDH19
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.99661914G>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000188374.1,