{{Rsnum
|rsid=3745760
|Gene=GLTSCR1
|Chromosome=19
|position=47702468
|Orientation=minus
|GMAF=0.3448
|Gene_s=GLTSCR1
|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 | 66.4 | 26.5 | 7.1
| HCB | 44.9 | 47.8 | 7.4
| JPT | 46.0 | 43.4 | 10.6
| YRI | 17.8 | 56.2 | 26.0
| ASW | 21.1 | 49.1 | 29.8
| CHB | 44.9 | 47.8 | 7.4
| CHD | 40.2 | 51.4 | 8.4
| GIH | 53.0 | 42.0 | 5.0
| LWK | 6.4 | 44.0 | 49.5
| MEX | 57.9 | 36.8 | 5.3
| MKK | 23.0 | 50.0 | 27.0
| TSI | 52.9 | 40.2 | 6.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22174851
|Trait=None
|Title=Genomewide association study for determinants of HIV-1 acquisition and viral set point in HIV-1 serodiscordant couples with quantified virus exposure.
|RiskAllele=
|Pval=8E-7
|OR=0
|ORtxt=None
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}