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rs111033373

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs111033373(A;A)
Make rs111033373(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position26462182
GeneOTOF
is asnp
is mentioned by
dbSNPrs111033373
ebirs111033373
HLIrs111033373
Exacrs111033373
Varsomers111033373
Maprs111033373
PheGenIrs111033373
hapmaprs111033373
1000 genomesrs111033373
hgdprs111033373
ensemblrs111033373
gopubmedrs111033373
geneviewrs111033373
scholarrs111033373
googlers111033373
pharmgkbrs111033373
gwascentralrs111033373
openSNPrs111033373
23andMers111033373
23andMe allrs111033373
SNP Nexus

SNPshotrs111033373
SNPdbers111033373
MSV3drs111033373
GWAS Ctlgrs111033373
Max Magnitude0
ClinVar
Risk rs111033373(A;A)
Alt rs111033373(A;A)
Reference rs111033373(G;G)
Significance Pathogenic
Disease Non-syndromic genetic deafness Deafness
Variation info
Gene OTOF
CLNDBN Non-syndromic genetic deafness Deafness, autosomal recessive 9
Reversed 1
HGVS NC_000002.11:g.26685050C>T
CLNSRC ClinVar
CLNACC RCV000041568.2, RCV000225066.1,