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rs397515609

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397515609(-;-)
Make rs397515609(-;C)
Make rs397515609(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position26460659
GeneOTOF
is asnp
is mentioned by
dbSNPrs397515609
ebirs397515609
HLIrs397515609
Exacrs397515609
Varsomers397515609
Maprs397515609
PheGenIrs397515609
hapmaprs397515609
1000 genomesrs397515609
hgdprs397515609
ensemblrs397515609
gopubmedrs397515609
geneviewrs397515609
scholarrs397515609
googlers397515609
pharmgkbrs397515609
gwascentralrs397515609
openSNPrs397515609
23andMers397515609
23andMe allrs397515609
SNP Nexus

SNPshotrs397515609
SNPdbers397515609
MSV3drs397515609
GWAS Ctlgrs397515609
Max Magnitude0
ClinVar
Risk rs397515609(C;C)
Alt rs397515609(C;C)
Reference rs397515609(;)
Significance Pathogenic
Disease Deafness
Variation info
Gene OTOF
CLNDBN Deafness, autosomal recessive 9
Reversed 1
HGVS NC_000002.11:g.26683528dupG
CLNSRC ClinVar GeneReviews
CLNACC RCV000056052.1,