{{Rsnum
|rsid=2234970
|Gene=SCD
|Chromosome=10
|position=102116311
|Orientation=plus
|GMAF=0.4238
|Gene_s=SCD
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 34.8 | 53.6 | 11.6
| HCB | 35.0 | 50.4 | 14.6
| JPT | 35.1 | 48.6 | 16.2
| YRI | 29.9 | 50.3 | 19.7
| ASW | 35.1 | 50.9 | 14.0
| CHB | 35.0 | 50.4 | 14.6
| CHD | 34.9 | 52.3 | 12.8
| GIH | 54.5 | 39.6 | 5.9
| LWK | 52.7 | 40.9 | 6.4
| MEX | 12.1 | 56.9 | 31.0
| MKK | 51.0 | 41.9 | 7.1
| TSI | 32.4 | 49.0 | 18.6
| HapMapRevision=28
}}{{PMID Auto
|PMID=24375980
|Title=Cardiometabolic risk factors are influenced by Stearoyl-CoA Desaturase (SCD) -1 gene polymorphisms and n-3 polyunsaturated fatty acid supplementation
}}

{{PMID Auto
|PMID=20565855
|Title=Genetic variation in lipid desaturases and its impact on the development of human disease.
|OA=1
}}

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