{{Rsnum
|rsid=2243639
|Gene=SFTPD
|Chromosome=10
|position=81701722
|Orientation=plus
|GMAF=0.258
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 37.2 | 44.2 | 18.6
| HCB | 60.6 | 36.5 | 2.9
| JPT | 54.0 | 38.9 | 7.1
| YRI | 100.0 | 0.0 | 0.0
| ASW | 84.2 | 14.0 | 1.8
| CHB | 60.6 | 36.5 | 2.9
| CHD | 66.1 | 28.4 | 5.5
| GIH | 60.4 | 31.7 | 7.9
| LWK | 98.2 | 1.8 | 0.0
| MEX | 39.7 | 46.6 | 13.8
| MKK | 92.3 | 7.7 | 0.0
| TSI | 30.4 | 52.0 | 17.6
| HapMapRevision=28
}}
{{PMID Auto
|PMID=19340882
|Title=Genetic variants in surfactant, pulmonary-associated protein D (SFTPD) and Japanese susceptibility to ulcerative colitis
}}

{{PMID|15726497|OA=1
}} Gene-environment interaction effects on the development of immune responses in the 1st year of life.

{{PMID|16385451|OA=1
}} A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease.

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

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

{{GET Evidence
|gene=SFTPD
|aa_change=Thr180Ala
|aa_change_short=T180A
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2243639
|overall_frequency_n=7691
|overall_frequency_d=10758
|overall_frequency=0.71491
|n_genomes=50
|n_genomes_annotated=0
|n_haplomes=81
|n_articles=0
|n_articles_annotated=0
|nblosum100=1
|autoscore=0
|webscore=N
}}

{{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 | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}