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rs121909059

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121909059(A;A)
Make rs121909059(A;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position121137648
GeneTECTA
is asnp
is mentioned by
dbSNPrs121909059
ebirs121909059
HLIrs121909059
Exacrs121909059
Varsomers121909059
Maprs121909059
PheGenIrs121909059
hapmaprs121909059
1000 genomesrs121909059
hgdprs121909059
ensemblrs121909059
gopubmedrs121909059
geneviewrs121909059
scholarrs121909059
googlers121909059
pharmgkbrs121909059
gwascentralrs121909059
openSNPrs121909059
23andMers121909059
23andMe allrs121909059
SNP Nexus

SNPshotrs121909059
SNPdbers121909059
MSV3drs121909059
GWAS Ctlgrs121909059
Max Magnitude0
OMIM602574
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121909059(A;A)
Alt rs121909059(A;A)
Reference rs121909059(T;T)
Significance Pathogenic
Disease Deafness
Variation info
Gene TECTA
CLNDBN Deafness, autosomal dominant 12
Reversed 0
HGVS NC_000011.9:g.121008357T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007431.2,