{{Rsnum
|rsid=4959039
|Chromosome=6
|position=29989292
|Orientation=plus
|GMAF=0.2617
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 40.7 | 49.6 | 9.7
| HCB | 50.4 | 41.6 | 8.0
| JPT | 57.5 | 36.3 | 6.2
| YRI | 85.7 | 12.9 | 1.4
| ASW | 70.2 | 29.8 | 0.0
| CHB | 50.4 | 41.6 | 8.0
| CHD | 45.0 | 47.7 | 7.3
| GIH | 77.0 | 21.0 | 2.0
| LWK | 69.1 | 29.1 | 1.8
| MEX | 55.2 | 41.4 | 3.4
| MKK | 84.6 | 15.4 | 0.0
| TSI | 59.8 | 32.4 | 7.8
| HapMapRevision=28
}}

[[rs4959039]] is a SNP located within the Class I HLA-G region of chromosome 6.

Independently of the influence of the (nearby) HLA-DRB1*1501 allele, the [[rs4959039]](G) was shown to be associated with increased risk for [[multiple sclerosis]] in a study of ~2,300 patients.{{PMID|20593013|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}