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rs111033383

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs111033383(A;A)
Make rs111033383(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position26479325
GeneOTOF
is asnp
is mentioned by
dbSNPrs111033383
ebirs111033383
HLIrs111033383
Exacrs111033383
Varsomers111033383
Maprs111033383
PheGenIrs111033383
hapmaprs111033383
1000 genomesrs111033383
hgdprs111033383
ensemblrs111033383
gopubmedrs111033383
geneviewrs111033383
scholarrs111033383
googlers111033383
pharmgkbrs111033383
gwascentralrs111033383
openSNPrs111033383
23andMers111033383
23andMe allrs111033383
SNP Nexus

SNPshotrs111033383
SNPdbers111033383
MSV3drs111033383
GWAS Ctlgrs111033383
Max Magnitude0
ClinVar
Risk rs111033383(A;A)
Alt rs111033383(A;A)
Reference rs111033383(G;G)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene OTOF
CLNDBN Non-syndromic genetic deafness
Reversed 1
HGVS NC_000002.11:g.26702193C>T
CLNSRC ClinVar
CLNACC RCV000041483.2,