Have questions? Visit https://www.reddit.com/r/SNPedia

rs111033384

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs111033384(-;-)
Make rs111033384(-;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position26460094
GeneOTOF
is asnp
is mentioned by
dbSNPrs111033384
ebirs111033384
HLIrs111033384
Exacrs111033384
Varsomers111033384
Maprs111033384
PheGenIrs111033384
hapmaprs111033384
1000 genomesrs111033384
hgdprs111033384
ensemblrs111033384
gopubmedrs111033384
geneviewrs111033384
scholarrs111033384
googlers111033384
pharmgkbrs111033384
gwascentralrs111033384
openSNPrs111033384
23andMers111033384
23andMe allrs111033384
SNP Nexus

SNPshotrs111033384
SNPdbers111033384
MSV3drs111033384
GWAS Ctlgrs111033384
Max Magnitude0
ClinVar
Risk rs111033384(;)
Alt rs111033384(;)
Reference rs111033384(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.26682962delC
CLNSRC
CLNACC RCV000154421.1,