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rs397515586

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397515586(G;G)
Make rs397515586(G;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position26480871
GeneOTOF
is asnp
is mentioned by
dbSNPrs397515586
ebirs397515586
HLIrs397515586
Exacrs397515586
Varsomers397515586
Maprs397515586
PheGenIrs397515586
hapmaprs397515586
1000 genomesrs397515586
hgdprs397515586
ensemblrs397515586
gopubmedrs397515586
geneviewrs397515586
scholarrs397515586
googlers397515586
pharmgkbrs397515586
gwascentralrs397515586
openSNPrs397515586
23andMers397515586
23andMe allrs397515586
SNP Nexus

SNPshotrs397515586
SNPdbers397515586
MSV3drs397515586
GWAS Ctlgrs397515586
Max Magnitude0
ClinVar
Risk rs397515586(G;G)
Alt rs397515586(G;G)
Reference rs397515586(T;T)
Significance Pathogenic
Disease Deafness
Variation info
Gene OTOF
CLNDBN Deafness, autosomal recessive 9
Reversed 1
HGVS NC_000002.11:g.26703739A>C
CLNSRC ClinVar GeneReviews
CLNACC RCV000056020.1,