rs796052816

Orientation

minus

Stabilized

minus

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

Make rs796052816(C;T)

Make rs796052816(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

100407247

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs796052816
dbSNP (classic)	rs796052816
ClinGen	rs796052816
ebi	rs796052816
HLI	rs796052816
Exac	rs796052816
Gnomad	rs796052816
Varsome	rs796052816
LitVar	rs796052816
Map	rs796052816
PheGenI	rs796052816
Biobank	rs796052816
1000 genomes	rs796052816
hgdp	rs796052816
ensembl	rs796052816
geneview	rs796052816
scholar	rs796052816
google	rs796052816
pharmgkb	rs796052816
gwascentral	rs796052816
openSNP	rs796052816
23andMe	rs796052816
SNPshot	rs796052816
SNPdbe	rs796052816
MSV3d	rs796052816
GWAS Ctlg	rs796052816

Max Magnitude

0

ClinVar
Risk	rs796052816(T;T)
Alt	rs796052816(T;T)
Reference	Rs796052816(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PCDH19
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.99662245G>A
CLNSRC
CLNACC	RCV000188369.1,