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rs397515610

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397515610(C;T)
Make rs397515610(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position26502301
GeneOTOF
is asnp
is mentioned by
dbSNPrs397515610
ebirs397515610
HLIrs397515610
Exacrs397515610
Varsomers397515610
Maprs397515610
PheGenIrs397515610
hapmaprs397515610
1000 genomesrs397515610
hgdprs397515610
ensemblrs397515610
gopubmedrs397515610
geneviewrs397515610
scholarrs397515610
googlers397515610
pharmgkbrs397515610
gwascentralrs397515610
openSNPrs397515610
23andMers397515610
23andMe allrs397515610
SNP Nexus

SNPshotrs397515610
SNPdbers397515610
MSV3drs397515610
GWAS Ctlgrs397515610
Max Magnitude0
ClinVar
Risk rs397515610(T;T)
Alt rs397515610(T;T)
Reference rs397515610(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene OTOF
CLNDBN Deafness, autosomal recessive 9
Reversed 1
HGVS NC_000002.11:g.26725169G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000056054.1,