rs796052814

Orientation

minus

Stabilized

minus

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

Make rs796052814(A;T)

Make rs796052814(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

100407357

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs796052814
dbSNP (classic)	rs796052814
ClinGen	rs796052814
ebi	rs796052814
HLI	rs796052814
Exac	rs796052814
Gnomad	rs796052814
Varsome	rs796052814
LitVar	rs796052814
Map	rs796052814
PheGenI	rs796052814
Biobank	rs796052814
1000 genomes	rs796052814
hgdp	rs796052814
ensembl	rs796052814
geneview	rs796052814
scholar	rs796052814
google	rs796052814
pharmgkb	rs796052814
gwascentral	rs796052814
openSNP	rs796052814
23andMe	rs796052814
SNPshot	rs796052814
SNPdbe	rs796052814
MSV3d	rs796052814
GWAS Ctlg	rs796052814

Max Magnitude

0

ClinVar
Risk	rs796052814(T;T)
Alt	rs796052814(T;T)
Reference	Rs796052814(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PCDH19
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.99662355T>A
CLNSRC
CLNACC	RCV000188367.1,