rs756414485

Orientation

plus

Stabilized

plus

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

Make rs756414485(A;A)

Make rs756414485(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

100350665

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs756414485
dbSNP (classic)	rs756414485
ClinGen	rs756414485
ebi	rs756414485
HLI	rs756414485
Exac	rs756414485
Gnomad	rs756414485
Varsome	rs756414485
LitVar	rs756414485
Map	rs756414485
PheGenI	rs756414485
Biobank	rs756414485
1000 genomes	rs756414485
hgdp	rs756414485
ensembl	rs756414485
geneview	rs756414485
scholar	rs756414485
google	rs756414485
pharmgkb	rs756414485
gwascentral	rs756414485
openSNP	rs756414485
23andMe	rs756414485
SNPshot	rs756414485
SNPdbe	rs756414485
MSV3d	rs756414485
GWAS Ctlg	rs756414485

Max Magnitude

0

ClinVar
Risk	rs756414485(A;A) rs756414485(C;C)
Alt	rs756414485(A;A) rs756414485(C;C)
Reference	Rs756414485(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PCDH19
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.99605663G>A
CLNSRC
CLNACC	RCV000188378.3,