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rs397515585

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515585(-;-)
Make rs397515585(-;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position26480980
GeneOTOF
is asnp
is mentioned by
dbSNPrs397515585
ebirs397515585
HLIrs397515585
Exacrs397515585
Varsomers397515585
Maprs397515585
PheGenIrs397515585
hapmaprs397515585
1000 genomesrs397515585
hgdprs397515585
ensemblrs397515585
gopubmedrs397515585
geneviewrs397515585
scholarrs397515585
googlers397515585
pharmgkbrs397515585
gwascentralrs397515585
openSNPrs397515585
23andMers397515585
23andMe allrs397515585
SNP Nexus

SNPshotrs397515585
SNPdbers397515585
MSV3drs397515585
GWAS Ctlgrs397515585
Max Magnitude0
ClinVar
Risk rs397515585(;)
Alt rs397515585(;)
Reference rs397515585(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene OTOF
CLNDBN Deafness, autosomal recessive 9
Reversed 1
HGVS NC_000002.11:g.26703848delC
CLNSRC ClinVar GeneReviews
CLNACC RCV000056019.1,