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rs121909064

From SNPedia

Merged intors121909061
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121909064(C;C)
Make rs121909064(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position121166703
GeneTECTA
is asnp
is mentioned by
dbSNPrs121909064
ebirs121909064
HLIrs121909064
Exacrs121909064
Varsomers121909064
Maprs121909064
PheGenIrs121909064
hapmaprs121909064
1000 genomesrs121909064
hgdprs121909064
ensemblrs121909064
gopubmedrs121909064
geneviewrs121909064
scholarrs121909064
googlers121909064
pharmgkbrs121909064
gwascentralrs121909064
openSNPrs121909064
23andMers121909064
23andMe allrs121909064
SNP Nexus

SNPshotrs121909064
SNPdbers121909064
MSV3drs121909064
GWAS Ctlgrs121909064
StatusMerged into rs121909061
Max Magnitude0
OMIM602574
Desc
Variant0011
Relatedalso
ClinVar
Risk rs121909064(C;C)
Alt rs121909064(C;C)
Reference rs121909064(T;T)
Significance Pathogenic
Disease Deafness
Variation info
Gene TECTA
CLNDBN Deafness, autosomal dominant 12
Reversed 0
HGVS NC_000011.9:g.121037412T>C
CLNSRC OMIM Allelic Variant
CLNACC SCV000027638.1,