rs911887

A SNP in the SFTPD gene on chromosome 10. Its most notable genotype is C;T: common in complete genomics

Gene
SFTPD
Location
Chr 1079,941,767 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
37%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. C;TMost notableGoodcommon in complete genomicsTypical · 0.044% of people

SNPedia records rs911887 on the minus strand: (A;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 11 HapMap populations.

  • AverageC;T 44%
  • European ancestry (Utah)C;T 47%
  • Han Chinese (Beijing)C;T 47%
  • Japanese (Tokyo)C;T 41%
  • Yoruba (Nigeria)C;T 50%
  • African ancestry (Southwest US)C;T 47%
  • Chinese (Denver)C;T 42%
  • Gujarati IndianC;T 50%
  • Luhya (Kenya)C;T 34%
  • Mexican ancestry (Los Angeles)C;T 48%
  • Maasai (Kenya)C;T 30%
  • TuscanC;T 49%

Other SFTPD SNPs

All SFTPD SNPs

Source and license

Adapted from rs911887 on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.

SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.