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

rs397515587

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397515587(-;-)
Make rs397515587(-;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position26480849
GeneOTOF
is asnp
is mentioned by
dbSNPrs397515587
ebirs397515587
HLIrs397515587
Exacrs397515587
Varsomers397515587
Maprs397515587
PheGenIrs397515587
hapmaprs397515587
1000 genomesrs397515587
hgdprs397515587
ensemblrs397515587
gopubmedrs397515587
geneviewrs397515587
scholarrs397515587
googlers397515587
pharmgkbrs397515587
gwascentralrs397515587
openSNPrs397515587
23andMers397515587
23andMe allrs397515587
SNP Nexus

SNPshotrs397515587
SNPdbers397515587
MSV3drs397515587
GWAS Ctlgrs397515587
Max Magnitude0
ClinVar
Risk rs397515587(;)
Alt rs397515587(;)
Reference rs397515587(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene OTOF
CLNDBN Deafness, autosomal recessive 9
Reversed 1
HGVS NC_000002.11:g.26703717delG
CLNSRC ClinVar GeneReviews
CLNACC RCV000056021.1,