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rs111033343

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs111033343(A;A)
Make rs111033343(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position83508665
GenePOU3F4
is asnp
is mentioned by
dbSNPrs111033343
ebirs111033343
HLIrs111033343
Exacrs111033343
Varsomers111033343
Maprs111033343
PheGenIrs111033343
hapmaprs111033343
1000 genomesrs111033343
hgdprs111033343
ensemblrs111033343
gopubmedrs111033343
geneviewrs111033343
scholarrs111033343
googlers111033343
pharmgkbrs111033343
gwascentralrs111033343
openSNPrs111033343
23andMers111033343
23andMe allrs111033343
SNP Nexus

SNPshotrs111033343
SNPdbers111033343
MSV3drs111033343
GWAS Ctlgrs111033343
Max Magnitude0
ClinVar
Risk rs111033343(A;A)
Alt rs111033343(A;A)
Reference rs111033343(G;G)
Significance Probable-Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene POU3F4
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000023.10:g.82763673G>A
CLNSRC ClinVar
CLNACC RCV000036254.2,