rs878853337

Orientation

plus

Stabilized

plus

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

Make rs878853337(C;G)

Make rs878853337(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

10

Position

71805841

Gene

CDH23

is a	snp
is	mentioned by
dbSNP	rs878853337
dbSNP (classic)	rs878853337
ClinGen	rs878853337
ebi	rs878853337
HLI	rs878853337
Exac	rs878853337
Gnomad	rs878853337
Varsome	rs878853337
LitVar	rs878853337
Map	rs878853337
PheGenI	rs878853337
Biobank	rs878853337
1000 genomes	rs878853337
hgdp	rs878853337
ensembl	rs878853337
geneview	rs878853337
scholar	rs878853337
google	rs878853337
pharmgkb	rs878853337
gwascentral	rs878853337
openSNP	rs878853337
23andMe	rs878853337
SNPshot	rs878853337
SNPdbe	rs878853337
MSV3d	rs878853337
GWAS Ctlg	rs878853337

Max Magnitude

0

ClinVar
Risk	rs878853337(G;G)
Alt	rs878853337(G;G)
Reference	Rs878853337(C;C)
Significance	Probable-Pathogenic
Disease	Retinal dystrophy
Variation	info
Gene	CDH23
CLNDBN	Retinal dystrophy
Reversed	0
HGVS	NC_000010.10:g.73565598C>G
CLNSRC
CLNACC	RCV000225547.1,