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rs397515583

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397515583(-;-)
Make rs397515583(-;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position26480988
GeneOTOF
is asnp
is mentioned by
dbSNPrs397515583
ebirs397515583
HLIrs397515583
Exacrs397515583
Varsomers397515583
Maprs397515583
PheGenIrs397515583
hapmaprs397515583
1000 genomesrs397515583
hgdprs397515583
ensemblrs397515583
gopubmedrs397515583
geneviewrs397515583
scholarrs397515583
googlers397515583
pharmgkbrs397515583
gwascentralrs397515583
openSNPrs397515583
23andMers397515583
23andMe allrs397515583
SNP Nexus

SNPshotrs397515583
SNPdbers397515583
MSV3drs397515583
GWAS Ctlgrs397515583
Max Magnitude0
ClinVar
Risk rs397515583(;)
Alt rs397515583(;)
Reference rs397515583(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene OTOF
CLNDBN Deafness, autosomal recessive 9
Reversed 1
HGVS NC_000002.11:g.26703856delG
CLNSRC ClinVar GeneReviews
CLNACC RCV000056017.1,