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rs397515607

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GAG;GAG) 0 common in clinvar
Make rs397515607(-;-)
Make rs397515607(-;GAG)
ReferenceGRCh38 38.1/141
Chromosome2
Position26461817
GeneOTOF
is asnp
is mentioned by
dbSNPrs397515607
ebirs397515607
HLIrs397515607
Exacrs397515607
Varsomers397515607
Maprs397515607
PheGenIrs397515607
hapmaprs397515607
1000 genomesrs397515607
hgdprs397515607
ensemblrs397515607
gopubmedrs397515607
geneviewrs397515607
scholarrs397515607
googlers397515607
pharmgkbrs397515607
gwascentralrs397515607
openSNPrs397515607
23andMers397515607
23andMe allrs397515607
SNP Nexus

SNPshotrs397515607
SNPdbers397515607
MSV3drs397515607
GWAS Ctlgrs397515607
Max Magnitude0
ClinVar
Risk rs397515607(;)
Alt rs397515607(;)
Reference rs397515607(GAG;GAG)
Significance Other
Disease Deafness Non-syndromic genetic deafness
Variation info
Gene OTOF
CLNDBN Deafness, autosomal recessive 9 Non-syndromic genetic deafness
Reversed 1
HGVS NC_000002.11:g.26684685_26684687delCTC
CLNSRC ClinVar GeneReviews
CLNACC RCV000056050.6, RCV000211735.1,