rs796052837

Orientation

minus

Stabilized

minus

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

Make rs796052837(C;G)

Make rs796052837(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

100408100

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs796052837
dbSNP (classic)	rs796052837
ClinGen	rs796052837
ebi	rs796052837
HLI	rs796052837
Exac	rs796052837
Gnomad	rs796052837
Varsome	rs796052837
LitVar	rs796052837
Map	rs796052837
PheGenI	rs796052837
Biobank	rs796052837
1000 genomes	rs796052837
hgdp	rs796052837
ensembl	rs796052837
geneview	rs796052837
scholar	rs796052837
google	rs796052837
pharmgkb	rs796052837
gwascentral	rs796052837
openSNP	rs796052837
23andMe	rs796052837
SNPshot	rs796052837
SNPdbe	rs796052837
MSV3d	rs796052837
GWAS Ctlg	rs796052837

Max Magnitude

0

ClinVar
Risk	rs796052837(G;G)
Alt	rs796052837(G;G)
Reference	Rs796052837(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PCDH19
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.99663098G>C
CLNSRC
CLNACC	RCV000188398.2,