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rs111033405

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs111033405(C;C)
Make rs111033405(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position26465753
GeneOTOF
is asnp
is mentioned by
dbSNPrs111033405
ebirs111033405
HLIrs111033405
Exacrs111033405
Varsomers111033405
Maprs111033405
PheGenIrs111033405
hapmaprs111033405
1000 genomesrs111033405
hgdprs111033405
ensemblrs111033405
gopubmedrs111033405
geneviewrs111033405
scholarrs111033405
googlers111033405
pharmgkbrs111033405
gwascentralrs111033405
openSNPrs111033405
23andMers111033405
23andMe allrs111033405
SNP Nexus

SNPshotrs111033405
SNPdbers111033405
MSV3drs111033405
GWAS Ctlgrs111033405
Max Magnitude0
ClinVar
Risk rs111033405(C;C)
Alt rs111033405(C;C)
Reference rs111033405(T;T)
Significance Other
Disease Deafness Non-syndromic genetic deafness
Variation info
Gene OTOF
CLNDBN Deafness, autosomal recessive 9 Non-syndromic genetic deafness
Reversed 1
HGVS NC_000002.11:g.26688621A>G
CLNSRC ClinVar
CLNACC RCV000041550.4, RCV000211733.1,