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rs111033345

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs111033345(C;T)
Make rs111033345(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position83508823
GenePOU3F4
is asnp
is mentioned by
dbSNPrs111033345
ebirs111033345
HLIrs111033345
Exacrs111033345
Varsomers111033345
Maprs111033345
PheGenIrs111033345
hapmaprs111033345
1000 genomesrs111033345
hgdprs111033345
ensemblrs111033345
gopubmedrs111033345
geneviewrs111033345
scholarrs111033345
googlers111033345
pharmgkbrs111033345
gwascentralrs111033345
openSNPrs111033345
23andMers111033345
23andMe allrs111033345
SNP Nexus

SNPshotrs111033345
SNPdbers111033345
MSV3drs111033345
GWAS Ctlgrs111033345
Max Magnitude0
ClinVar
Risk rs111033345(T;T)
Alt rs111033345(T;T)
Reference rs111033345(C;C)
Significance Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene POU3F4
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000023.10:g.82763831C>T
CLNSRC ClinVar
CLNACC RCV000036255.2,