rs796052801

Orientation

minus

Stabilized

minus

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

Make rs796052801(C;G)

Make rs796052801(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

100408125

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs796052801
dbSNP (classic)	rs796052801
ClinGen	rs796052801
ebi	rs796052801
HLI	rs796052801
Exac	rs796052801
Gnomad	rs796052801
Varsome	rs796052801
LitVar	rs796052801
Map	rs796052801
PheGenI	rs796052801
Biobank	rs796052801
1000 genomes	rs796052801
hgdp	rs796052801
ensembl	rs796052801
geneview	rs796052801
scholar	rs796052801
google	rs796052801
pharmgkb	rs796052801
gwascentral	rs796052801
openSNP	rs796052801
23andMe	rs796052801
SNPshot	rs796052801
SNPdbe	rs796052801
MSV3d	rs796052801
GWAS Ctlg	rs796052801

Max Magnitude

0

ClinVar
Risk	rs796052801(G;G)
Alt	rs796052801(G;G)
Reference	Rs796052801(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PCDH19
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.99663123G>C
CLNSRC
CLNACC	RCV000188351.1,