rs796052827

Orientation

minus

Stabilized

minus

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

Make rs796052827(-;-)

Make rs796052827(-;A)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

100407793

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs796052827
dbSNP (classic)	rs796052827
ClinGen	rs796052827
ebi	rs796052827
HLI	rs796052827
Exac	rs796052827
Gnomad	rs796052827
Varsome	rs796052827
LitVar	rs796052827
Map	rs796052827
PheGenI	rs796052827
Biobank	rs796052827
1000 genomes	rs796052827
hgdp	rs796052827
ensembl	rs796052827
geneview	rs796052827
scholar	rs796052827
google	rs796052827
pharmgkb	rs796052827
gwascentral	rs796052827
openSNP	rs796052827
23andMe	rs796052827
SNPshot	rs796052827
SNPdbe	rs796052827
MSV3d	rs796052827
GWAS Ctlg	rs796052827

Max Magnitude

0

ClinVar
Risk	rs796052827(-;-)
Alt	rs796052827(-;-)
Reference	Rs796052827(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PCDH19
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.99662791delT
CLNSRC
CLNACC	RCV000188387.1,