rs3088308

A SNP in the SFTPD gene on chromosome 10. Its most notable genotype is A;A: common in clinvar

Gene
SFTPD
Location
Chr 1079,938,112 (GRCh38)
Highest magnitude
0.0Typical
Tested on
Not on consumer chips

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;AMost notableGoodcommon in clinvarTypical · 0.095% of people

On SNPedia: (A;A). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 4 HapMap populations.

  • AverageA;A 95%
  • European ancestry (Utah)A;A 89%
  • Han Chinese (Beijing)A;A 96%
  • Japanese (Tokyo)A;A 93%
  • Yoruba (Nigeria)A;A 100%

Other SFTPD SNPs

All SFTPD SNPs

Source and license

Adapted from rs3088308 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.