rs3752752

Orientation

minus

Stabilized

minus

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

Make rs3752752(A;G)

Make rs3752752(G;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

71695444

Gene

CDH23

is a	snp
is	mentioned by
dbSNP	rs3752752
dbSNP (classic)	rs3752752
ClinGen	rs3752752
ebi	rs3752752
HLI	rs3752752
Exac	rs3752752
Gnomad	rs3752752
Varsome	rs3752752
LitVar	rs3752752
Map	rs3752752
PheGenI	rs3752752
Biobank	rs3752752
1000 genomes	rs3752752
hgdp	rs3752752
ensembl	rs3752752
geneview	rs3752752
scholar	rs3752752
google	rs3752752
pharmgkb	rs3752752
gwascentral	rs3752752
openSNP	rs3752752
23andMe	rs3752752
SNPshot	rs3752752
SNPdbe	rs3752752
MSV3d	rs3752752
GWAS Ctlg	rs3752752

GMAF

0.4215

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

[PMID 24448297] Genetic Variants of CDH23 Associated With Noise-Induced Hearing Loss

ClinVar
Risk	rs3752752(G;G)
Alt	rs3752752(G;G)
Reference	Rs3752752(A;A)
Significance	Probable-non-pathogenic
Disease	not specified Nonsyndromic Hearing Loss Retinitis pigmentosa-deafness syndrome
Variation	info
Gene	CDH23
CLNDBN	not specified Nonsyndromic Hearing Loss, Recessive Retinitis pigmentosa-deafness syndrome
Reversed	1
HGVS	NC_000010.10:g.73455201T\x3d; NC_000010.10:g.73455201T>C
CLNSRC	ClinVar
CLNACC	RCV000154334.1, RCV000039126.3, RCV000349454.1, RCV000394281.1,

[PMID 32306668] [Relationship research among CDH23 gene and the risk of noise-induced hearing loss].