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rs111033447

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs111033447(A;A)
Make rs111033447(A;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position26495011
GeneOTOF
is asnp
is mentioned by
dbSNPrs111033447
ClinGenrs111033447
ebirs111033447
HLIrs111033447
Exacrs111033447
Varsomers111033447
Maprs111033447
PheGenIrs111033447
hapmaprs111033447
1000 genomesrs111033447
hgdprs111033447
ensemblrs111033447
gopubmedrs111033447
geneviewrs111033447
scholarrs111033447
googlers111033447
pharmgkbrs111033447
gwascentralrs111033447
openSNPrs111033447
23andMers111033447
23andMe allrs111033447
SNP Nexus

SNPshotrs111033447
SNPdbers111033447
MSV3drs111033447
GWAS Ctlgrs111033447
Max Magnitude0
ClinVar
Risk rs111033447(A;A) rs111033447(T;T)
Alt rs111033447(A;A) rs111033447(T;T)
Reference Rs111033447(C;C)
Significance Probable-Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene OTOF
CLNDBN Non-syndromic genetic deafness
Reversed 1
HGVS NC_000002.11:g.26717879G>T
CLNSRC ClinVar
CLNACC RCV000041590.2,