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rs111033341

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs111033341(G;G)
Make rs111033341(G;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position26489209
GeneOTOF
is asnp
is mentioned by
dbSNPrs111033341
ebirs111033341
HLIrs111033341
Exacrs111033341
Varsomers111033341
Maprs111033341
PheGenIrs111033341
hapmaprs111033341
1000 genomesrs111033341
hgdprs111033341
ensemblrs111033341
gopubmedrs111033341
geneviewrs111033341
scholarrs111033341
googlers111033341
pharmgkbrs111033341
gwascentralrs111033341
openSNPrs111033341
23andMers111033341
23andMe allrs111033341
SNP Nexus

SNPshotrs111033341
SNPdbers111033341
MSV3drs111033341
GWAS Ctlgrs111033341
Max Magnitude0
ClinVar
Risk rs111033341(G;G)
Alt rs111033341(G;G)
Reference rs111033341(T;T)
Significance Probable-Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene OTOF
CLNDBN Non-syndromic genetic deafness
Reversed 1
HGVS NC_000002.11:g.26712077A>C
CLNSRC ClinVar
CLNACC RCV000041453.2,