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rs397515606

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397515606(G;G)
Make rs397515606(G;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position26461845
GeneOTOF
is asnp
is mentioned by
dbSNPrs397515606
ebirs397515606
HLIrs397515606
Exacrs397515606
Varsomers397515606
Maprs397515606
PheGenIrs397515606
hapmaprs397515606
1000 genomesrs397515606
hgdprs397515606
ensemblrs397515606
gopubmedrs397515606
geneviewrs397515606
scholarrs397515606
googlers397515606
pharmgkbrs397515606
gwascentralrs397515606
openSNPrs397515606
23andMers397515606
23andMe allrs397515606
SNP Nexus

SNPshotrs397515606
SNPdbers397515606
MSV3drs397515606
GWAS Ctlgrs397515606
Max Magnitude0
ClinVar
Risk rs397515606(G;G)
Alt rs397515606(G;G)
Reference rs397515606(T;T)
Significance Pathogenic
Disease Deafness
Variation info
Gene OTOF
CLNDBN Deafness, autosomal recessive 9
Reversed 1
HGVS NC_000002.11:g.26684713A>C
CLNSRC ClinVar GeneReviews
CLNACC RCV000056049.1,