rs796052831

Orientation

minus

Stabilized

minus

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

Make rs796052831(-;-)

Make rs796052831(-;C)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

100407290

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs796052831
dbSNP (classic)	rs796052831
ClinGen	rs796052831
ebi	rs796052831
HLI	rs796052831
Exac	rs796052831
Gnomad	rs796052831
Varsome	rs796052831
LitVar	rs796052831
Map	rs796052831
PheGenI	rs796052831
Biobank	rs796052831
1000 genomes	rs796052831
hgdp	rs796052831
ensembl	rs796052831
geneview	rs796052831
scholar	rs796052831
google	rs796052831
pharmgkb	rs796052831
gwascentral	rs796052831
openSNP	rs796052831
23andMe	rs796052831
SNPshot	rs796052831
SNPdbe	rs796052831
MSV3d	rs796052831
GWAS Ctlg	rs796052831

Max Magnitude

0

ClinVar
Risk	rs796052831(-;-)
Alt	rs796052831(-;-)
Reference	Rs796052831(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PCDH19
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.99662288delG
CLNSRC
CLNACC	RCV000188392.1,