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rs397515580

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397515580(-;-)
Make rs397515580(-;G)
Make rs397515580(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position26484498
GeneOTOF
is asnp
is mentioned by
dbSNPrs397515580
ebirs397515580
HLIrs397515580
Exacrs397515580
Varsomers397515580
Maprs397515580
PheGenIrs397515580
hapmaprs397515580
1000 genomesrs397515580
hgdprs397515580
ensemblrs397515580
gopubmedrs397515580
geneviewrs397515580
scholarrs397515580
googlers397515580
pharmgkbrs397515580
gwascentralrs397515580
openSNPrs397515580
23andMers397515580
23andMe allrs397515580
SNP Nexus

SNPshotrs397515580
SNPdbers397515580
MSV3drs397515580
GWAS Ctlgrs397515580
Max Magnitude0
ClinVar
Risk rs397515580(G;G)
Alt rs397515580(G;G)
Reference rs397515580(;)
Significance Pathogenic
Disease Deafness
Variation info
Gene OTOF
CLNDBN Deafness, autosomal recessive 9
Reversed 1
HGVS NC_000002.11:g.26707367dupC
CLNSRC ClinVar GeneReviews
CLNACC RCV000056012.1,