rs10103355

A SNP in the ASAH1 gene on chromosome 8. Its most notable genotype is A;A: common in clinvar

Gene
ASAH1
Location
Chr 818,061,425 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
14%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;AMost notableGoodcommon in clinvarTypical · 0.07% of people
  2. G;GGoodcommon in complete genomicsTypical · 0.067% of people

On SNPedia: (A;A), (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.

  • AverageA;A 7% G;G 67%
  • European ancestry (Utah)A;A 0% G;G 95%
  • Han Chinese (Beijing)A;A 4% G;G 73%
  • Japanese (Tokyo)A;A 3% G;G 81%
  • Yoruba (Nigeria)A;A 16% G;G 27%
  • African ancestry (Southwest US)A;A 23% G;G 33%
  • Chinese (Denver)A;A 2% G;G 74%
  • Gujarati IndianA;A 0% G;G 95%
  • Luhya (Kenya)A;A 12% G;G 33%
  • Mexican ancestry (Los Angeles)A;A 0% G;G 93%
  • Maasai (Kenya)A;A 14% G;G 41%
  • TuscanA;A 0% G;G 96%

Other ASAH1 SNPs

All ASAH1 SNPs

Source and license

Adapted from rs10103355 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.