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rs397515602

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515602(G;T)
Make rs397515602(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position26467110
GeneOTOF
is asnp
is mentioned by
dbSNPrs397515602
ebirs397515602
HLIrs397515602
Exacrs397515602
Varsomers397515602
Maprs397515602
PheGenIrs397515602
hapmaprs397515602
1000 genomesrs397515602
hgdprs397515602
ensemblrs397515602
gopubmedrs397515602
geneviewrs397515602
scholarrs397515602
googlers397515602
pharmgkbrs397515602
gwascentralrs397515602
openSNPrs397515602
23andMers397515602
23andMe allrs397515602
SNP Nexus

SNPshotrs397515602
SNPdbers397515602
MSV3drs397515602
GWAS Ctlgrs397515602
Max Magnitude0
ClinVar
Risk rs397515602(T;T)
Alt rs397515602(T;T)
Reference rs397515602(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene OTOF
CLNDBN Deafness, autosomal recessive 9
Reversed 1
HGVS NC_000002.11:g.26689978C>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000056042.1,