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rs267607107

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607107(A;A)
Make rs267607107(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position121166665
GeneTECTA
is asnp
is mentioned by
dbSNPrs267607107
ebirs267607107
HLIrs267607107
Exacrs267607107
Varsomers267607107
Maprs267607107
PheGenIrs267607107
hapmaprs267607107
1000 genomesrs267607107
hgdprs267607107
ensemblrs267607107
gopubmedrs267607107
geneviewrs267607107
scholarrs267607107
googlers267607107
pharmgkbrs267607107
gwascentralrs267607107
openSNPrs267607107
23andMers267607107
23andMe allrs267607107
SNP Nexus

SNPshotrs267607107
SNPdbers267607107
MSV3drs267607107
GWAS Ctlgrs267607107
Max Magnitude0
ClinVar
Risk rs267607107(A;A)
Alt rs267607107(A;A)
Reference rs267607107(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene TECTA
CLNDBN Deafness, autosomal dominant 12
Reversed 0
HGVS NC_000011.9:g.121037374G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007428.2,