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

rs111033370

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs111033370(-;-)
Make rs111033370(-;A)
Make rs111033370(A;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position26477451
GeneOTOF
is asnp
is mentioned by
dbSNPrs111033370
ebirs111033370
HLIrs111033370
Exacrs111033370
Varsomers111033370
Maprs111033370
PheGenIrs111033370
hapmaprs111033370
1000 genomesrs111033370
hgdprs111033370
ensemblrs111033370
gopubmedrs111033370
geneviewrs111033370
scholarrs111033370
googlers111033370
pharmgkbrs111033370
gwascentralrs111033370
openSNPrs111033370
23andMers111033370
23andMe allrs111033370
SNP Nexus

SNPshotrs111033370
SNPdbers111033370
MSV3drs111033370
GWAS Ctlgrs111033370
Max Magnitude0
ClinVar
Risk rs111033370(A;A)
Alt rs111033370(A;A)
Reference rs111033370(;)
Significance Probable-Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene OTOF
CLNDBN Non-syndromic genetic deafness
Reversed 1
HGVS NC_000002.11:g.26700319_26700320insT
CLNSRC ClinVar
CLNACC RCV000041491.2,