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rs397515605

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515605(A;A)
Make rs397515605(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position26462177
GeneOTOF
is asnp
is mentioned by
dbSNPrs397515605
ebirs397515605
HLIrs397515605
Exacrs397515605
Varsomers397515605
Maprs397515605
PheGenIrs397515605
hapmaprs397515605
1000 genomesrs397515605
hgdprs397515605
ensemblrs397515605
gopubmedrs397515605
geneviewrs397515605
scholarrs397515605
googlers397515605
pharmgkbrs397515605
gwascentralrs397515605
openSNPrs397515605
23andMers397515605
23andMe allrs397515605
SNP Nexus

SNPshotrs397515605
SNPdbers397515605
MSV3drs397515605
GWAS Ctlgrs397515605
Max Magnitude0
ClinVar
Risk rs397515605(A;A)
Alt rs397515605(A;A)
Reference rs397515605(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene OTOF
CLNDBN Deafness, autosomal recessive 9
Reversed 1
HGVS NC_000002.11:g.26685045C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000056048.1,