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rs397515601

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515601(G;T)
Make rs397515601(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position26467364
GeneOTOF
is asnp
is mentioned by
dbSNPrs397515601
ebirs397515601
HLIrs397515601
Exacrs397515601
Varsomers397515601
Maprs397515601
PheGenIrs397515601
hapmaprs397515601
1000 genomesrs397515601
hgdprs397515601
ensemblrs397515601
gopubmedrs397515601
geneviewrs397515601
scholarrs397515601
googlers397515601
pharmgkbrs397515601
gwascentralrs397515601
openSNPrs397515601
23andMers397515601
23andMe allrs397515601
SNP Nexus

SNPshotrs397515601
SNPdbers397515601
MSV3drs397515601
GWAS Ctlgrs397515601
Max Magnitude0
ClinVar
Risk rs397515601(T;T)
Alt rs397515601(T;T)
Reference rs397515601(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene OTOF
CLNDBN Deafness, autosomal recessive 9
Reversed 1
HGVS NC_000002.11:g.26690232C>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000056041.1, RCV000225066.1,