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rs80356604

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80356604(A;A)
Make rs80356604(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position26460851
GeneOTOF
is asnp
is mentioned by
dbSNPrs80356604
ebirs80356604
HLIrs80356604
Exacrs80356604
Varsomers80356604
Maprs80356604
PheGenIrs80356604
hapmaprs80356604
1000 genomesrs80356604
hgdprs80356604
ensemblrs80356604
gopubmedrs80356604
geneviewrs80356604
scholarrs80356604
googlers80356604
pharmgkbrs80356604
gwascentralrs80356604
openSNPrs80356604
23andMers80356604
23andMe allrs80356604
SNP Nexus

SNPshotrs80356604
SNPdbers80356604
MSV3drs80356604
GWAS Ctlgrs80356604
Max Magnitude0
ClinVar
Risk rs80356604(A;A)
Alt rs80356604(A;A)
Reference rs80356604(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene OTOF
CLNDBN Deafness, autosomal recessive 9
Reversed 1
HGVS NC_000002.11:g.26683719C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000021072.1,


[PMID 16226319] Results of cochlear implantation in two children with mutations in the OTOF gene.