{{Rsnum
|rsid=968566
|Gene=GJA3
|Chromosome=13
|position=20142394
|Orientation=minus
|ReferenceAllele=C
|MissenseAllele=A
|GMAF=0.01699
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=GJA3
}}{{Venter SNP
|rsid=968566
|allele=T
|frequency=
|uid=1103649163177
|type=homozygous_SNP
|hugo=GJA3
|ensembl gene=ENSG00000121743
|ensembl transcript=ENST00000241125
|sift=TOLERATED
|disease=Defects in GJA3 are the cause of zonular pulverulent cataract type 3 (CZP3) (MIM:601885). CZP3 is a form of autosomal dominant congenital cataract.
}}

{{GET Evidence
|gene=GJA3
|aa_change=Leu299Met
|aa_change_short=L299M
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs968566
|overall_frequency_n=9865
|overall_frequency_d=10192
|overall_frequency=0.967916
|n_genomes=17
|n_genomes_annotated=0
|n_haplomes=34
|n_articles=0
|n_articles_annotated=0
|gene_in_genetests=Y
|nblosum100=-3
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}