{{Rsnum
|rsid=6916861
|Gene=FYN
|Chromosome=6
|position=111661054
|Orientation=plus
|GMAF=0.219
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=FYN
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 67.3 | 30.1 | 2.7
| HCB | 56.9 | 38.0 | 5.1
| JPT | 46.0 | 40.7 | 13.3
| YRI | 32.7 | 49.7 | 17.7
| ASW | 43.9 | 47.4 | 8.8
| CHB | 56.9 | 38.0 | 5.1
| CHD | 49.1 | 42.6 | 8.3
| GIH | 93.1 | 6.9 | 0.0
| LWK | 39.1 | 42.7 | 18.2
| MEX | 84.5 | 15.5 | 0.0
| MKK | 52.6 | 36.5 | 10.9
| TSI | 78.4 | 21.6 | 0.0
| HapMapRevision=28
}}
{{PMID Auto
|PMID=19468241
|Title=Functional impact of endotoxin receptor CD14 polymorphisms on transcriptional activity
}}

{{PMID Auto
|PMID=24852829
|Title=The association of single nucleotide polymorphism of the Fyn gene with sporadic Alzheimer's disease in the Chinese Han population
}}
{{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}}