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rs397515589

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515589(A;A)
Make rs397515589(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position26480274
GeneOTOF
is asnp
is mentioned by
dbSNPrs397515589
ebirs397515589
HLIrs397515589
Exacrs397515589
Varsomers397515589
Maprs397515589
PheGenIrs397515589
hapmaprs397515589
1000 genomesrs397515589
hgdprs397515589
ensemblrs397515589
gopubmedrs397515589
geneviewrs397515589
scholarrs397515589
googlers397515589
pharmgkbrs397515589
gwascentralrs397515589
openSNPrs397515589
23andMers397515589
23andMe allrs397515589
SNP Nexus

SNPshotrs397515589
SNPdbers397515589
MSV3drs397515589
GWAS Ctlgrs397515589
Max Magnitude0
ClinVar
Risk rs397515589(A;A)
Alt rs397515589(A;A)
Reference rs397515589(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene OTOF
CLNDBN Deafness, autosomal recessive 9
Reversed 1
HGVS NC_000002.11:g.26703142C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000056023.1,