rs11592462

Orientation

plus

Stabilized

plus

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

Make rs11592462(C;G)

Make rs11592462(G;G)

Reference

GRCh38.p7 38.3/149

Chromosome

10

Position

71790360

Gene	CDH23, MIR7152

is a	snp
is	mentioned by
dbSNP	rs11592462
dbSNP (classic)	rs11592462
ClinGen	rs11592462
ebi	rs11592462
HLI	rs11592462
Exac	rs11592462
Gnomad	rs11592462
Varsome	rs11592462
LitVar	rs11592462
Map	rs11592462
PheGenI	rs11592462
Biobank	rs11592462
1000 genomes	rs11592462
hgdp	rs11592462
ensembl	rs11592462
geneview	rs11592462
scholar	rs11592462
google	rs11592462
pharmgkb	rs11592462
gwascentral	rs11592462
openSNP	rs11592462
23andMe	rs11592462
SNPshot	rs11592462
SNPdbe	rs11592462
MSV3d	rs11592462
GWAS Ctlg	rs11592462

Max Magnitude

0

?	(C;C) (C;G) (G;G)	28

[PMID 25445010] Pathway analysis for a genome-wide association study of pneumoconiosis.

ClinVar
Risk	rs11592462(G;G)
Alt	rs11592462(G;G)
Reference	Rs11592462(C;C)
Significance	Probable-non-pathogenic
Disease	not specified Nonsyndromic Hearing Loss Retinitis pigmentosa-deafness syndrome
Variation	info
Gene	MIR7152 CDH23
CLNDBN	not specified Nonsyndromic Hearing Loss, Recessive Retinitis pigmentosa-deafness syndrome
Reversed	0
HGVS	NC_000010.10:g.73550117C>G
CLNSRC
CLNACC	RCV000039232.7, RCV000338564.1, RCV000405485.1,

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