rs796052820

Orientation

minus

Stabilized

minus

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

Make rs796052820(C;T)

Make rs796052820(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

100406743

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs796052820
dbSNP (classic)	rs796052820
ClinGen	rs796052820
ebi	rs796052820
HLI	rs796052820
Exac	rs796052820
Gnomad	rs796052820
Varsome	rs796052820
LitVar	rs796052820
Map	rs796052820
PheGenI	rs796052820
Biobank	rs796052820
1000 genomes	rs796052820
hgdp	rs796052820
ensembl	rs796052820
geneview	rs796052820
scholar	rs796052820
google	rs796052820
pharmgkb	rs796052820
gwascentral	rs796052820
openSNP	rs796052820
23andMe	rs796052820
SNPshot	rs796052820
SNPdbe	rs796052820
MSV3d	rs796052820
GWAS Ctlg	rs796052820

Max Magnitude

0

ClinVar
Risk	rs796052820(T;T)
Alt	rs796052820(T;T)
Reference	Rs796052820(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PCDH19
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.99661741G>A
CLNSRC
CLNACC	RCV000188375.2,