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rs397515600

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397515600(C;T)
Make rs397515600(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position26467435
GeneOTOF
is asnp
is mentioned by
dbSNPrs397515600
ebirs397515600
HLIrs397515600
Exacrs397515600
Varsomers397515600
Maprs397515600
PheGenIrs397515600
hapmaprs397515600
1000 genomesrs397515600
hgdprs397515600
ensemblrs397515600
gopubmedrs397515600
geneviewrs397515600
scholarrs397515600
googlers397515600
pharmgkbrs397515600
gwascentralrs397515600
openSNPrs397515600
23andMers397515600
23andMe allrs397515600
SNP Nexus

SNPshotrs397515600
SNPdbers397515600
MSV3drs397515600
GWAS Ctlgrs397515600
Max Magnitude0
ClinVar
Risk rs397515600(G,T;G,T)
Alt rs397515600(G,T;G,T)
Reference rs397515600(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene OTOF
CLNDBN Deafness, autosomal recessive 9
Reversed 1
HGVS NC_000002.11:g.26690303G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000056040.1,