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rs397515608

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515608(A;A)
Make rs397515608(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position26460997
GeneOTOF
is asnp
is mentioned by
dbSNPrs397515608
ebirs397515608
HLIrs397515608
Exacrs397515608
Varsomers397515608
Maprs397515608
PheGenIrs397515608
hapmaprs397515608
1000 genomesrs397515608
hgdprs397515608
ensemblrs397515608
gopubmedrs397515608
geneviewrs397515608
scholarrs397515608
googlers397515608
pharmgkbrs397515608
gwascentralrs397515608
openSNPrs397515608
23andMers397515608
23andMe allrs397515608
SNP Nexus

SNPshotrs397515608
SNPdbers397515608
MSV3drs397515608
GWAS Ctlgrs397515608
Max Magnitude0
ClinVar
Risk rs397515608(A;A)
Alt rs397515608(A;A)
Reference rs397515608(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene OTOF
CLNDBN Deafness, autosomal recessive 9
Reversed 1
HGVS NC_000002.11:g.26683865C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000056051.1,