{{Rsnum
|rsid=10918196
|Gene=SAMM50
|Chromosome=1
|position=165478920
|Orientation=plus
|GMAF=0.4582
|Gene_s=SAMM50
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 10.6 | 53.1 | 36.3
| HCB | 65.2 | 31.8 | 3.0
| JPT | 48.6 | 45.9 | 5.4
| YRI | 6.1 | 30.6 | 63.3
| ASW | 12.3 | 31.6 | 56.1
| CHB | 65.2 | 31.8 | 3.0
| CHD | 66.1 | 32.1 | 1.8
| GIH | 19.6 | 51.5 | 28.9
| LWK | 3.6 | 34.5 | 61.8
| MEX | 21.1 | 52.6 | 26.3
| MKK | 4.5 | 35.3 | 60.3
| TSI | 7.8 | 54.9 | 37.3
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=22903471
  |Trait=Lentiform nucleus volume
  |Title=Genome-wide association identifies genetic variants associated with lentiform nucleus volume in N = 1345 young and elderly subjects.
  |RiskAllele=C
  |Pval=9E-6
  |OR=93.94
  |ORtxt=[NR] unit increase
  }}

{{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}}