rs796052794

Orientation

minus

Stabilized

minus

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

Make rs796052794(G;T)

Make rs796052794(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

100408507

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs796052794
dbSNP (classic)	rs796052794
ClinGen	rs796052794
ebi	rs796052794
HLI	rs796052794
Exac	rs796052794
Gnomad	rs796052794
Varsome	rs796052794
LitVar	rs796052794
Map	rs796052794
PheGenI	rs796052794
Biobank	rs796052794
1000 genomes	rs796052794
hgdp	rs796052794
ensembl	rs796052794
geneview	rs796052794
scholar	rs796052794
google	rs796052794
pharmgkb	rs796052794
gwascentral	rs796052794
openSNP	rs796052794
23andMe	rs796052794
SNPshot	rs796052794
SNPdbe	rs796052794
MSV3d	rs796052794
GWAS Ctlg	rs796052794

Max Magnitude

0

ClinVar
Risk	rs796052794(T;T)
Alt	rs796052794(T;T)
Reference	Rs796052794(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PCDH19
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.99663505C>A
CLNSRC
CLNACC	RCV000188342.1,