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rs878853242

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853242(C;T)
Make rs878853242(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position83508559
GenePOU3F4
is asnp
is mentioned by
dbSNPrs878853242
ebirs878853242
HLIrs878853242
Exacrs878853242
Varsomers878853242
Maprs878853242
PheGenIrs878853242
hapmaprs878853242
1000 genomesrs878853242
hgdprs878853242
ensemblrs878853242
gopubmedrs878853242
geneviewrs878853242
scholarrs878853242
googlers878853242
pharmgkbrs878853242
gwascentralrs878853242
openSNPrs878853242
23andMers878853242
23andMe allrs878853242
SNP Nexus

SNPshotrs878853242
SNPdbers878853242
MSV3drs878853242
GWAS Ctlgrs878853242
Max Magnitude0
ClinVar
Risk rs878853242(T;T)
Alt rs878853242(T;T)
Reference rs878853242(C;C)
Significance Pathogenic
Disease Deafness
Variation info
Gene POU3F4
CLNDBN Deafness, X-linked 2
Reversed 0
HGVS NC_000023.10:g.82763567C>T
CLNSRC
CLNACC RCV000225042.1,