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rs111033342

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs111033342(A;A)
Make rs111033342(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position26467234
GeneOTOF
is asnp
is mentioned by
dbSNPrs111033342
ebirs111033342
HLIrs111033342
Exacrs111033342
Varsomers111033342
Maprs111033342
PheGenIrs111033342
hapmaprs111033342
1000 genomesrs111033342
hgdprs111033342
ensemblrs111033342
gopubmedrs111033342
geneviewrs111033342
scholarrs111033342
googlers111033342
pharmgkbrs111033342
gwascentralrs111033342
openSNPrs111033342
23andMers111033342
23andMe allrs111033342
SNP Nexus

SNPshotrs111033342
SNPdbers111033342
MSV3drs111033342
GWAS Ctlgrs111033342
Max Magnitude0
ClinVar
Risk rs111033342(A;A)
Alt rs111033342(A;A)
Reference rs111033342(G;G)
Significance Probable-Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene OTOF
CLNDBN Non-syndromic genetic deafness
Reversed 1
HGVS NC_000002.11:g.26690102C>T
CLNSRC ClinVar
CLNACC RCV000041540.2,