rs796052839

Orientation

minus

Stabilized

minus

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

Make rs796052839(A;G)

Make rs796052839(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

100407579

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs796052839
dbSNP (classic)	rs796052839
ClinGen	rs796052839
ebi	rs796052839
HLI	rs796052839
Exac	rs796052839
Gnomad	rs796052839
Varsome	rs796052839
LitVar	rs796052839
Map	rs796052839
PheGenI	rs796052839
Biobank	rs796052839
1000 genomes	rs796052839
hgdp	rs796052839
ensembl	rs796052839
geneview	rs796052839
scholar	rs796052839
google	rs796052839
pharmgkb	rs796052839
gwascentral	rs796052839
openSNP	rs796052839
23andMe	rs796052839
SNPshot	rs796052839
SNPdbe	rs796052839
MSV3d	rs796052839
GWAS Ctlg	rs796052839

Max Magnitude

0

ClinVar
Risk	rs796052839(G;G)
Alt	rs796052839(G;G)
Reference	Rs796052839(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PCDH19
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.99662577T>C; NC_000023.10:g.99662577T>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000188401.3, RCV000494063.1,