rs796052829

Orientation

minus

Stabilized

minus

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

Make rs796052829(-;-)

Make rs796052829(-;A)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

100407222

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs796052829
dbSNP (classic)	rs796052829
ClinGen	rs796052829
ebi	rs796052829
HLI	rs796052829
Exac	rs796052829
Gnomad	rs796052829
Varsome	rs796052829
LitVar	rs796052829
Map	rs796052829
PheGenI	rs796052829
Biobank	rs796052829
1000 genomes	rs796052829
hgdp	rs796052829
ensembl	rs796052829
geneview	rs796052829
scholar	rs796052829
google	rs796052829
pharmgkb	rs796052829
gwascentral	rs796052829
openSNP	rs796052829
23andMe	rs796052829
SNPshot	rs796052829
SNPdbe	rs796052829
MSV3d	rs796052829
GWAS Ctlg	rs796052829

Max Magnitude

0

ClinVar
Risk	rs796052829(-;-)
Alt	rs796052829(-;-)
Reference	Rs796052829(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PCDH19
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.99662220delT
CLNSRC
CLNACC	RCV000188389.1,