rs4775041

A SNP in the LOC101928635 gene on chromosome 15. Its most notable genotype is C;C: lowest phosphatidylethanolamine values

Gene
LOC101928635
Location
Chr 1558,382,496 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
21%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. C;CMost notableNot ratedlowest phosphatidylethanolamine valuesTypical · 0.05% of people
  2. C;GNot ratedintermediate phosphatidylethanolamine valuesTypical · 0.029% of people
  3. G;GNot ratedhighest phosphatidylethanolamine valuesTypical · 0.066% of people

On SNPedia: (C;C), (C;G), (G;G). 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.

  • AverageC;C 5% C;G 29% G;G 66%
  • European ancestry (Utah)C;C 8% C;G 41% G;G 52%
  • Han Chinese (Beijing)C;C 4% C;G 29% G;G 67%
  • Japanese (Tokyo)C;C 7% C;G 36% G;G 57%
  • Yoruba (Nigeria)C;C 2% C;G 10% G;G 89%

Conditions, medicines and genes

Other LOC101928635 SNPs

All LOC101928635 SNPs

Notes

From SNPedia

Notes

rs4775041 is a SNP located near the LIPC gene. A study of metabolite concentrations in the blood of 284 adult males from Southern Germany determined that several SNPs were associated either directly with a metabolite range or with a ratio of metabolites. The rarer rs4775041(G) allele was associated with increased phosphatidylethanolamine values. 322px|thumb|left|

Source and license

Adapted from rs4775041 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.