rs796052802

Orientation

minus

Stabilized

minus

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

Make rs796052802(C;T)

Make rs796052802(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

100407979

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs796052802
dbSNP (classic)	rs796052802
ClinGen	rs796052802
ebi	rs796052802
HLI	rs796052802
Exac	rs796052802
Gnomad	rs796052802
Varsome	rs796052802
LitVar	rs796052802
Map	rs796052802
PheGenI	rs796052802
Biobank	rs796052802
1000 genomes	rs796052802
hgdp	rs796052802
ensembl	rs796052802
geneview	rs796052802
scholar	rs796052802
google	rs796052802
pharmgkb	rs796052802
gwascentral	rs796052802
openSNP	rs796052802
23andMe	rs796052802
SNPshot	rs796052802
SNPdbe	rs796052802
MSV3d	rs796052802
GWAS Ctlg	rs796052802

Max Magnitude

0

ClinVar
Risk	rs796052802(G;G) rs796052802(T;T)
Alt	rs796052802(G;G) rs796052802(T;T)
Reference	Rs796052802(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PCDH19
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.99662977G>A
CLNSRC
CLNACC	RCV000188352.1,