rs1468063

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

Gene
FAS
Location
Chr 1089,015,534 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. C;CMost notableGoodcommon in clinvarTypical · 0.058% of people

SNPedia records rs1468063 on the minus strand: (G;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;C 58%
  • European ancestry (Utah)C;C 83%
  • Han Chinese (Beijing)C;C 40%
  • Japanese (Tokyo)C;C 39%
  • Yoruba (Nigeria)C;C 57%
  • African ancestry (Southwest US)C;C 63%
  • Chinese (Denver)C;C 33%
  • Gujarati IndianC;C 71%
  • Luhya (Kenya)C;C 55%
  • Mexican ancestry (Los Angeles)C;C 61%
  • Maasai (Kenya)C;C 66%
  • TuscanC;C 73%

Other FAS SNPs

All FAS SNPs

Source and license

Adapted from rs1468063 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.