{{Rsnum
|rsid = 6639946
|geno1 = (C;C)
|geno2 = (C;G)
|geno3 = (G;G)
|Gene=VCX
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=G
|Chromosome=X
|position=7843604
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=VCX
}}{{Venter SNP
|rsid=6639946
|allele=G
|frequency=
|uid=1103673004407
|type=homozygous_SNP
|hugo=VCX
|ensembl gene=ENSG00000182583
|ensembl transcript=ENST00000381059
|sift=TOLERATED
|disease=Defects in VCX3A are associated with some forms of X- linked nonspecific mental retardation.
}}

{{on chip | HumanOmni1Quad}}