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rs111033455

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs111033455(A;G)
Make rs111033455(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position26460749
GeneOTOF
is asnp
is mentioned by
dbSNPrs111033455
ebirs111033455
HLIrs111033455
Exacrs111033455
Varsomers111033455
Maprs111033455
PheGenIrs111033455
hapmaprs111033455
1000 genomesrs111033455
hgdprs111033455
ensemblrs111033455
gopubmedrs111033455
geneviewrs111033455
scholarrs111033455
googlers111033455
pharmgkbrs111033455
gwascentralrs111033455
openSNPrs111033455
23andMers111033455
23andMe allrs111033455
SNP Nexus

SNPshotrs111033455
SNPdbers111033455
MSV3drs111033455
GWAS Ctlgrs111033455
Max Magnitude0
ClinVar
Risk rs111033455(G;G)
Alt rs111033455(G;G)
Reference rs111033455(A;A)
Significance Probable-Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene OTOF
CLNDBN Non-syndromic genetic deafness
Reversed 1
HGVS NC_000002.11:g.26683617T>C
CLNSRC ClinVar
CLNACC RCV000041582.2,