rs796052826

Orientation

minus

Stabilized

minus

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

Make rs796052826(-;-)

Make rs796052826(-;G)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

100408074

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs796052826
dbSNP (classic)	rs796052826
ClinGen	rs796052826
ebi	rs796052826
HLI	rs796052826
Exac	rs796052826
Gnomad	rs796052826
Varsome	rs796052826
LitVar	rs796052826
Map	rs796052826
PheGenI	rs796052826
Biobank	rs796052826
1000 genomes	rs796052826
hgdp	rs796052826
ensembl	rs796052826
geneview	rs796052826
scholar	rs796052826
google	rs796052826
pharmgkb	rs796052826
gwascentral	rs796052826
openSNP	rs796052826
23andMe	rs796052826
SNPshot	rs796052826
SNPdbe	rs796052826
MSV3d	rs796052826
GWAS Ctlg	rs796052826

Max Magnitude

0

ClinVar
Risk	rs796052826(-;-)
Alt	rs796052826(-;-)
Reference	Rs796052826(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PCDH19
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.99663072delC
CLNSRC
CLNACC	RCV000188386.1,