{{Rsnum
|rsid=911887
|Gene=SFTPD
|Chromosome=10
|position=81701523
|Orientation=minus
|GMAF=0.3673
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 38.1 | 46.9 | 15.0
| HCB | 35.8 | 47.4 | 16.8
| JPT | 50.4 | 40.7 | 8.8
| YRI | 35.4 | 49.7 | 15.0
| ASW | 45.6 | 47.4 | 7.0
| CHB | 35.8 | 47.4 | 16.8
| CHD | 45.0 | 42.2 | 12.8
| GIH | 29.7 | 49.5 | 20.8
| LWK | 45.5 | 33.6 | 20.9
| MEX | 46.6 | 48.3 | 5.2
| MKK | 64.7 | 29.5 | 5.8
| TSI | 46.1 | 49.0 | 4.9
| HapMapRevision=28
}}{{PMID Auto
|PMID=19340882
|Title=Genetic variants in surfactant, pulmonary-associated protein D (SFTPD) and Japanese susceptibility to ulcerative colitis
}}

{{PMID Auto
|PMID=20448057
|Title=Polymorphisms in surfactant protein-D are associated with chronic obstructive pulmonary disease.
|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}}