{{Rsnum
|rsid=6836703
|Gene=ART3
|Chromosome=4
|position=76108994
|Orientation=plus
|GMAF=0.2383
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ART3
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 23.1 | 76.9
| HCB | 28.9 | 42.2 | 28.9
| JPT | 18.2 | 54.5 | 27.3
| YRI | 6.5 | 46.8 | 46.8
| ASW | 0.0 | 0.0 | 0.0
| CHB | 28.9 | 42.2 | 28.9
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}[[rs6836703]] is one of several tightly linked SNPs in the [[ART3]] gene found in a study of ~400 infertile males to be associated with somewhat increased risk of the type of [[male infertility]] known as non-obstructive azoospermia. The odds ratio reported for [[rs6836703]](A) carriers is 1.34 (CI:1.11â€“1.63, p=0.0025).{{PMID|18266473|OA=1
}}

An almost equivalent [[ART3]] SNP is [[rs14773]], for which it's also the minor allele ((C) in this case) reported to represent increased risk for azoospermia and which is in tight linkage with [[rs6836703]]. Two other [[ART3]] SNPs, [[rs11097230]] and [[rs17001385]], also achieved statistical significance, yet for them, the minor alleles were associated with reduced risk for azoospermia.{{PMID|18266473|OA=1
}}

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