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rs397515598

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515598(C;C)
Make rs397515598(C;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position26474562
GeneOTOF
is asnp
is mentioned by
dbSNPrs397515598
ebirs397515598
HLIrs397515598
Exacrs397515598
Varsomers397515598
Maprs397515598
PheGenIrs397515598
hapmaprs397515598
1000 genomesrs397515598
hgdprs397515598
ensemblrs397515598
gopubmedrs397515598
geneviewrs397515598
scholarrs397515598
googlers397515598
pharmgkbrs397515598
gwascentralrs397515598
openSNPrs397515598
23andMers397515598
23andMe allrs397515598
SNP Nexus

SNPshotrs397515598
SNPdbers397515598
MSV3drs397515598
GWAS Ctlgrs397515598
Max Magnitude0
ClinVar
Risk rs397515598(A,C;A,C)
Alt rs397515598(A,C;A,C)
Reference rs397515598(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene OTOF
CLNDBN Deafness, autosomal recessive 9
Reversed 1
HGVS NC_000002.11:g.26697430C>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000056035.1,