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rs121909062

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909062(A;A)
Make rs121909062(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position121187894
GeneTECTA
is asnp
is mentioned by
dbSNPrs121909062
ebirs121909062
HLIrs121909062
Exacrs121909062
Varsomers121909062
Maprs121909062
PheGenIrs121909062
hapmaprs121909062
1000 genomesrs121909062
hgdprs121909062
ensemblrs121909062
gopubmedrs121909062
geneviewrs121909062
scholarrs121909062
googlers121909062
pharmgkbrs121909062
gwascentralrs121909062
openSNPrs121909062
23andMers121909062
23andMe allrs121909062
SNP Nexus

SNPshotrs121909062
SNPdbers121909062
MSV3drs121909062
GWAS Ctlgrs121909062
Max Magnitude0
OMIM602574
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121909062(A;A)
Alt rs121909062(A;A)
Reference rs121909062(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene TECTA
CLNDBN Deafness, autosomal dominant 12
Reversed 0
HGVS NC_000011.9:g.121058603G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007436.2,