rs398123603

Orientation

minus

Stabilized

minus

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

Make rs398123603(A;G)

Make rs398123603(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

100408224

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs398123603
dbSNP (classic)	rs398123603
ClinGen	rs398123603
ebi	rs398123603
HLI	rs398123603
Exac	rs398123603
Gnomad	rs398123603
Varsome	rs398123603
LitVar	rs398123603
Map	rs398123603
PheGenI	rs398123603
Biobank	rs398123603
1000 genomes	rs398123603
hgdp	rs398123603
ensembl	rs398123603
geneview	rs398123603
scholar	rs398123603
google	rs398123603
pharmgkb	rs398123603
gwascentral	rs398123603
openSNP	rs398123603
23andMe	rs398123603
SNPshot	rs398123603
SNPdbe	rs398123603
MSV3d	rs398123603
GWAS Ctlg	rs398123603

Max Magnitude

0

ClinVar
Risk	rs398123603(G;G)
Alt	rs398123603(G;G)
Reference	Rs398123603(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PCDH19
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.99663222T>C
CLNSRC
CLNACC	RCV000079608.4,