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rs111033349

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs111033349(A;A)
Make rs111033349(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position26461854
GeneOTOF
is asnp
is mentioned by
dbSNPrs111033349
ebirs111033349
HLIrs111033349
Exacrs111033349
Varsomers111033349
Maprs111033349
PheGenIrs111033349
hapmaprs111033349
1000 genomesrs111033349
hgdprs111033349
ensemblrs111033349
gopubmedrs111033349
geneviewrs111033349
scholarrs111033349
googlers111033349
pharmgkbrs111033349
gwascentralrs111033349
openSNPrs111033349
23andMers111033349
23andMe allrs111033349
SNP Nexus

SNPshotrs111033349
SNPdbers111033349
MSV3drs111033349
GWAS Ctlgrs111033349
Max Magnitude0
ClinVar
Risk rs111033349(A;A)
Alt rs111033349(A;A)
Reference rs111033349(G;G)
Significance Probable-Pathogenic
Disease Non-syndromic genetic deafness not provided
Variation info
Gene OTOF
CLNDBN Non-syndromic genetic deafness not provided
Reversed 1
HGVS NC_000002.11:g.26684722C>T
CLNSRC
CLNACC RCV000041571.2, RCV000171287.1,