{{Rsnum
|rsid=13289
|Gene=SLC45A2
|Chromosome=5
|position=33986304
|Orientation=minus
|GMAF=0.4582
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=SLC45A2
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 49.2 | 38.5 | 12.3
| HCB | 46.7 | 42.2 | 11.1
| JPT | 36.4 | 54.5 | 9.1
| YRI | 11.3 | 30.6 | 58.1
| ASW | 0.0 | 0.0 | 0.0
| CHB | 46.7 | 42.2 | 11.1
| 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
}}

{{omim
|desc=SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 5; SHEP5
|id=227240
|rsnum=13289
}}

{{omim
|desc=SOLUTE CARRIER FAMILY 45, MEMBER 2; SLC45A2
|id=606202
|rsnum=13289
}}

{{PMID Auto
|PMID=17358008
|Title=Promoter polymorphisms in the MATP (SLC45A2) gene are associated with normal human skin color variation.
}}

{{PMID Auto
|PMID=18483556
|Title=A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation.
|OA=1
}}

{{PMID Auto
|PMID=19340012
|Title=Genome-wide association study of tanning phenotype in a population of European ancestry.
|OA=1
}}

{{PMID Auto
|PMID=19384953
|Title=Genetic variants in pigmentation genes, pigmentary phenotypes, and risk of skin cancer in Caucasians.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}