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rs397515588

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515588(A;A)
Make rs397515588(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position26480809
GeneOTOF
is asnp
is mentioned by
dbSNPrs397515588
ebirs397515588
HLIrs397515588
Exacrs397515588
Varsomers397515588
Maprs397515588
PheGenIrs397515588
hapmaprs397515588
1000 genomesrs397515588
hgdprs397515588
ensemblrs397515588
gopubmedrs397515588
geneviewrs397515588
scholarrs397515588
googlers397515588
pharmgkbrs397515588
gwascentralrs397515588
openSNPrs397515588
23andMers397515588
23andMe allrs397515588
SNP Nexus

SNPshotrs397515588
SNPdbers397515588
MSV3drs397515588
GWAS Ctlgrs397515588
Max Magnitude0
ClinVar
Risk rs397515588(A;A)
Alt rs397515588(A;A)
Reference rs397515588(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene OTOF
CLNDBN Deafness, autosomal recessive 9
Reversed 1
HGVS NC_000002.11:g.26703677C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000056022.1,