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rs397515604

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397515604(-;-)
Make rs397515604(-;T)
Make rs397515604(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position26464055
GeneOTOF
is asnp
is mentioned by
dbSNPrs397515604
ebirs397515604
HLIrs397515604
Exacrs397515604
Varsomers397515604
Maprs397515604
PheGenIrs397515604
hapmaprs397515604
1000 genomesrs397515604
hgdprs397515604
ensemblrs397515604
gopubmedrs397515604
geneviewrs397515604
scholarrs397515604
googlers397515604
pharmgkbrs397515604
gwascentralrs397515604
openSNPrs397515604
23andMers397515604
23andMe allrs397515604
SNP Nexus

SNPshotrs397515604
SNPdbers397515604
MSV3drs397515604
GWAS Ctlgrs397515604
Max Magnitude0
ClinVar
Risk rs397515604(T;T)
Alt rs397515604(T;T)
Reference rs397515604(;)
Significance Pathogenic
Disease Deafness
Variation info
Gene OTOF
CLNDBN Deafness, autosomal recessive 9
Reversed 1
HGVS NC_000002.11:g.26686924dupA
CLNSRC ClinVar GeneReviews
CLNACC RCV000056046.1,