{{Rsnum
|rsid=721917
|Gene=SFTPD
|Chromosome=10
|position=81706324
|Orientation=minus
|GMAF=0.4683
|Assembly=GRCh37.p2
|GenomeBuild=37.2
|dbSNPBuild=134
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 23.0 | 41.6 | 35.4
| HCB | 35.8 | 55.5 | 8.8
| JPT | 35.4 | 48.7 | 15.9
| YRI | 13.6 | 45.6 | 40.8
| ASW | 14.0 | 57.9 | 28.1
| CHB | 35.8 | 55.5 | 8.8
| CHD | 36.1 | 53.7 | 10.2
| GIH | 59.4 | 35.6 | 5.0
| LWK | 19.1 | 40.9 | 40.0
| MEX | 19.0 | 48.3 | 32.8
| MKK | 14.8 | 51.0 | 34.2
| TSI | 11.8 | 49.0 | 39.2
| HapMapRevision=28
}}{{PMID Auto
|PMID=21934714
|Title=Involvement of surfactant protein D in emphysema revealed by genetic association study
|OA=1
}}

{{PMID Auto
|PMID=22509983
|Title=Association Between Genetic Variations In Surfactant Protein D and Emphysema, Interstitial Pneumonia, and Lung Cancer in a Japanese Population
}}

{{PMID|16846490|OA=1
}} Lemierre's syndrome and genetic polymorphisms: a case report.

{{PMID|20018039|OA=1
}} Associating multiple longitudinal traits with high-dimensional single-nucleotide polymorphism data: application to the Framingham Heart Study.

{{PMID|20448057|OA=1
}} Polymorphisms in surfactant protein-D are associated with chronic obstructive pulmonary disease.

{{PMID|21790524|OA=1
}} Genetic variants and monoallelic expression of surfactant protein-D in inflammatory bowel disease.

{{GET Evidence
|gene=SFTPD
|aa_change=Met31Thr
|aa_change_short=M31T
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs721917
|overall_frequency_n=4423
|overall_frequency_d=10758
|overall_frequency=0.411136
|n_genomes=37
|n_genomes_annotated=0
|n_haplomes=42
|n_articles=0
|n_articles_annotated=0
|nblosum100=2
|autoscore=0
|webscore=N
}}

{{PMID Auto
|PMID=23577114
|Title=Common Genetic Variants of Surfactant Protein-D (SP-D) Are Associated with Type 2 Diabetes
|OA=1
}}

{{PMID Auto
|PMID=25015576
|Title=Surfactant Protein-D-Encoding Gene Variant Polymorphisms Are Linked to Respiratory Outcome in Premature Infants
}}
{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}