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rs397515603

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397515603(C;T)
Make rs397515603(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position26465010
GeneOTOF
is asnp
is mentioned by
dbSNPrs397515603
ebirs397515603
HLIrs397515603
Exacrs397515603
Varsomers397515603
Maprs397515603
PheGenIrs397515603
hapmaprs397515603
1000 genomesrs397515603
hgdprs397515603
ensemblrs397515603
gopubmedrs397515603
geneviewrs397515603
scholarrs397515603
googlers397515603
pharmgkbrs397515603
gwascentralrs397515603
openSNPrs397515603
23andMers397515603
23andMe allrs397515603
SNP Nexus

SNPshotrs397515603
SNPdbers397515603
MSV3drs397515603
GWAS Ctlgrs397515603
Max Magnitude0
ClinVar
Risk rs397515603(T;T)
Alt rs397515603(T;T)
Reference rs397515603(C;C)
Significance Other
Disease Deafness
Variation info
Gene OTOF
CLNDBN Deafness, autosomal recessive 9
Reversed 1
HGVS NC_000002.11:g.26687878G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000056045.1,