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rs397515581

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397515581(-;-)
Make rs397515581(-;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position26483618
GeneOTOF
is asnp
is mentioned by
dbSNPrs397515581
ebirs397515581
HLIrs397515581
Exacrs397515581
Varsomers397515581
Maprs397515581
PheGenIrs397515581
hapmaprs397515581
1000 genomesrs397515581
hgdprs397515581
ensemblrs397515581
gopubmedrs397515581
geneviewrs397515581
scholarrs397515581
googlers397515581
pharmgkbrs397515581
gwascentralrs397515581
openSNPrs397515581
23andMers397515581
23andMe allrs397515581
SNP Nexus

SNPshotrs397515581
SNPdbers397515581
MSV3drs397515581
GWAS Ctlgrs397515581
Max Magnitude0
ClinVar
Risk rs397515581(;)
Alt rs397515581(;)
Reference rs397515581(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene OTOF
CLNDBN Deafness, autosomal recessive 9
Reversed 1
HGVS NC_000002.11:g.26706486delG
CLNSRC ClinVar GeneReviews
CLNACC RCV000056014.1,