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rs111033446

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs111033446(-;-)
Make rs111033446(-;AA)
ReferenceGRCh38 38.1/141
Chromosome2
Position26460988
GeneOTOF
is asnp
is mentioned by
dbSNPrs111033446
ebirs111033446
HLIrs111033446
Exacrs111033446
Varsomers111033446
Maprs111033446
PheGenIrs111033446
hapmaprs111033446
1000 genomesrs111033446
hgdprs111033446
ensemblrs111033446
gopubmedrs111033446
geneviewrs111033446
scholarrs111033446
googlers111033446
pharmgkbrs111033446
gwascentralrs111033446
openSNPrs111033446
23andMers111033446
23andMe allrs111033446
SNP Nexus

SNPshotrs111033446
SNPdbers111033446
MSV3drs111033446
GWAS Ctlgrs111033446
Max Magnitude0
ClinVar
Risk rs111033446(;)
Alt rs111033446(;)
Reference rs111033446(AA;AA)
Significance Probable-Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene OTOF
CLNDBN Non-syndromic genetic deafness
Reversed 1
HGVS NC_000002.11:g.26683856_26683857delTT
CLNSRC ClinVar
CLNACC RCV000041577.2,