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rs397515435

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515435(A;A)
Make rs397515435(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position26480968
GeneOTOF
is asnp
is mentioned by
dbSNPrs397515435
ebirs397515435
HLIrs397515435
Exacrs397515435
Varsomers397515435
Maprs397515435
PheGenIrs397515435
hapmaprs397515435
1000 genomesrs397515435
hgdprs397515435
ensemblrs397515435
gopubmedrs397515435
geneviewrs397515435
scholarrs397515435
googlers397515435
pharmgkbrs397515435
gwascentralrs397515435
openSNPrs397515435
23andMers397515435
23andMe allrs397515435
SNP Nexus

SNPshotrs397515435
SNPdbers397515435
MSV3drs397515435
GWAS Ctlgrs397515435
Max Magnitude0
ClinVar
Risk rs397515435(A;A)
Alt rs397515435(A;A)
Reference rs397515435(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene OTOF
CLNDBN Deafness, autosomal recessive 9
Reversed 1
HGVS NC_000002.11:g.26703836C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000033199.2,