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rs267606932

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606932(A;A)
Make rs267606932(A;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position54183451
GenePCDH15
is asnp
is mentioned by
dbSNPrs267606932
ebirs267606932
HLIrs267606932
Exacrs267606932
Varsomers267606932
Maprs267606932
PheGenIrs267606932
hapmaprs267606932
1000 genomesrs267606932
hgdprs267606932
ensemblrs267606932
gopubmedrs267606932
geneviewrs267606932
scholarrs267606932
googlers267606932
pharmgkbrs267606932
gwascentralrs267606932
openSNPrs267606932
23andMers267606932
23andMe allrs267606932
SNP Nexus

SNPshotrs267606932
SNPdbers267606932
MSV3drs267606932
GWAS Ctlgrs267606932
Max Magnitude0
ClinVar
Risk rs267606932(A;A)
Alt rs267606932(A;A)
Reference rs267606932(T;T)
Significance Pathogenic
Disease Deafness
Variation info
Gene PCDH15
CLNDBN Deafness, autosomal recessive 23
Reversed 1
HGVS NC_000010.10:g.55943211A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005225.2,