{{Rsnum
|rsid=5921979
|Gene=POU3F4
|Chromosome=X
|position=83509034
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=C
|GMAF=0.1076
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{Venter SNP
|rsid=5921979
|allele=C
|frequency=
|uid=1103673053681
|type=homozygous_SNP
|hugo=POU3F4
|ensembl gene=ENSG00000196767
|ensembl transcript=ENST00000373200
|sift=TOLERATED
|disease=Defects in POU3F4 are a cause of X-linked deafness type 3 (DFN3) (MIM:304400). DFN3 is a mixed type of deafness characterized by both conductive hearing loss resulting from stapes (perilymphatic gusher) fixation and progressive sensorineural deafness.
}}

{{on chip | HumanOmni1Quad}}