Have questions? Visit https://www.reddit.com/r/SNPedia

rs397515584

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515584(A;A)
Make rs397515584(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position26480982
GeneOTOF
is asnp
is mentioned by
dbSNPrs397515584
ebirs397515584
HLIrs397515584
Exacrs397515584
Varsomers397515584
Maprs397515584
PheGenIrs397515584
hapmaprs397515584
1000 genomesrs397515584
hgdprs397515584
ensemblrs397515584
gopubmedrs397515584
geneviewrs397515584
scholarrs397515584
googlers397515584
pharmgkbrs397515584
gwascentralrs397515584
openSNPrs397515584
23andMers397515584
23andMe allrs397515584
SNP Nexus

SNPshotrs397515584
SNPdbers397515584
MSV3drs397515584
GWAS Ctlgrs397515584
Max Magnitude0
ClinVar
Risk rs397515584(A,C;A,C)
Alt rs397515584(A,C;A,C)
Reference rs397515584(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene OTOF
CLNDBN Deafness, autosomal recessive 9
Reversed 1
HGVS NC_000002.11:g.26703850C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000056018.1,