rs796052796

Orientation

minus

Stabilized

minus

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

Make rs796052796(A;A)

Make rs796052796(A;C)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

100408229

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs796052796
dbSNP (classic)	rs796052796
ClinGen	rs796052796
ebi	rs796052796
HLI	rs796052796
Exac	rs796052796
Gnomad	rs796052796
Varsome	rs796052796
LitVar	rs796052796
Map	rs796052796
PheGenI	rs796052796
Biobank	rs796052796
1000 genomes	rs796052796
hgdp	rs796052796
ensembl	rs796052796
geneview	rs796052796
scholar	rs796052796
google	rs796052796
pharmgkb	rs796052796
gwascentral	rs796052796
openSNP	rs796052796
23andMe	rs796052796
SNPshot	rs796052796
SNPdbe	rs796052796
MSV3d	rs796052796
GWAS Ctlg	rs796052796

Max Magnitude

0

ClinVar
Risk	rs796052796(A;A) rs796052796(T;T)
Alt	rs796052796(A;A) rs796052796(T;T)
Reference	Rs796052796(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PCDH19
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.99663227G>C; NC_000023.10:g.99663227G>T
CLNSRC
CLNACC	RCV000494296.1, RCV000188346.1,