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rs11592462

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs11592462(C;G)
Make rs11592462(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome10
Position71790360
GeneCDH23, MIR7152
is asnp
is mentioned by
dbSNPrs11592462
dbSNP (old)rs11592462
ClinGenrs11592462
ebirs11592462
HLIrs11592462
Exacrs11592462
Gnomadrs11592462
Varsomers11592462
Maprs11592462
PheGenIrs11592462
Biobankrs11592462
1000 genomesrs11592462
hgdprs11592462
ensemblrs11592462
gopubmedrs11592462
geneviewrs11592462
scholarrs11592462
googlers11592462
pharmgkbrs11592462
gwascentralrs11592462
openSNPrs11592462
23andMers11592462
23andMe allrs11592462
SNPshotrs11592462
SNPdbers11592462
MSV3drs11592462
GWAS Ctlgrs11592462
Max Magnitude0
? (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,