Genetic variant

rs1535

rs1535 is a single-letter difference in human DNA, on chromosome 11. Carrying it does not, on its own, mean you have or will develop any condition.

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What is this?

Your DNA is a long sequence of four letters. At a few million positions, people commonly differ by a single letter; each of those positions is called a SNP (“snip”), and rs1535 is the catalogue number of one of them. Which letters you carry there — one copy from each parent — is your genotype.

4 IQ points for breastfeeding with the AA or AG genotypes Breastfeeding and IQ [GWAS:Response to s...

From SNPedia

Why might it matter?

ClinVar holds no clinical classification for this variant. That is the usual case: most catalogued variants have no known effect on health.

Do I have this variant?

If you have taken a consumer DNA test (23andMe, AncestryDNA and similar), you can download its raw data file and check. Create a free account, upload the file, and this page will show the letters you carry at rs1535, if your test read this position.

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Connect this with your blood results

A gene is a fixed instruction; a blood test shows what your body is doing now. CheckMyBloods reads the two side by side, so a variant can be set against the markers it could plausibly affect.

Blood markers do not diagnose a genetic condition, and a variant does not explain a blood result on its own. Together, with symptoms and family history, they give a clinician context.

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What should I do next?

  1. Find out whether you carry it. Reading about a variant says nothing about you until you know your genotype.
  2. Put it in context. Add your blood results, so the variant can be read against what your body is doing.
  3. Ask questions. Dr. Hemsworth, our AI assistant, can explain this variant and your results in plain English.
  4. Take anything that worries you to a professional. A GP or genetic counsellor can order a confirmatory test and interpret it with your history.
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This page is general information drawn from public research databases. It cannot diagnose anything, and it is not a substitute for advice from a doctor or genetic counsellor who knows your history.

Technical details

dbSNP ID
rs1535
Position
chr11:61830500

Genome-wide association studies (20)

TraitRisk alleleOR / betaP-valueStudy
Lysophosphatidylethanolamine_22:4_[M-H]1- levels G OR 0.35 2E-281 PubMed
Lysophosphatidylcholine_20:4_[M+H]1+ levels G OR 0.41 5E-258 PubMed
Plasma omega-3 polyunsaturated fatty acid levels (docosapentaenoic acid) A β 0.07 3E-152 PubMed
Phosphatidylethanolamine_38:4_[M-H]1- levels G OR 0.23 5E-150 PubMed
Cholesteryl ester_20:5_[M+NH4]1+ levels G OR 0.3 2E-146 PubMed
Phosphatidylcholine_37:4_[M+H]1+/Phosphatidylethanolamine_40:4_[M+H]1+/Phosphatidate_42:5_[M+NH4]1+ levels G OR 0.37 2E-128 PubMed
Fatty acid(20:4)_[M-H]1- levels G OR 0.19 8E-120 PubMed
Phosphatidylcholine_38:5_[M+H]1+/Phosphatidylethanolamine_41:5_[M+H]1+/Phosphatidate_43:6_[M+NH4]1+ levels G OR 0.35 1E-117 PubMed
Phosphatidylcholine_36:3_[M+H]1+/Phosphatidylethanolamine_39:3_[M+H]1+/Phosphatidate_41:4_[M+NH4]1+ levels G OR 0.33 1E-112 PubMed
Diacylglycerol (18:1_20:3) levels G OR 0.48 3E-101 PubMed
1-docosapentaenoyl-GPC (22:5n3) levels A OR 0.22 5E-99 PubMed
Diacylglycerol_38:3_[M+H-H2O]1+ levels G OR 0.17 3E-98 PubMed
Phosphatidylcholine_35:3_[M+H]1+/Phosphatidylethanolamine_38:3_[M+H]1+/Phosphatidate_40:4_[M+NH4]1+ levels G OR 0.22 5E-95 PubMed
Phosphatidylinositol_36:3_[M-H]1- levels G OR 0.22 4E-91 PubMed
Phosphatidylethanolamine (18:0_18:2) levels G OR 0.46 1E-90 PubMed
Phosphatidylethanolamine_39:4_[M-H]1- levels G OR 0.19 2E-80 PubMed
Phosphatidylethanolamine_38:3_[M-H]1- levels G OR 0.15 3E-80 PubMed
Phosphatidylcholine_34:2_[M+H]1+/Phosphatidylethanolamine_37:2_[M+H]1+/Phosphatidate_39:3_[M+NH4]1+ levels G OR 0.22 5E-79 PubMed
Phosphatidylcholine_35:4_[M+H]1+/Phosphatidylethanolamine_38:4_[M+H]1+/Phosphatidate_40:5_[M+NH4]1+ levels G OR 0.22 5E-76 PubMed
Phosphatidylcholine_31:2_[M+H]1+/Phosphatidylethanolamine_34:2_[M+H]1+/Phosphatidate_36:3_[M+NH4]1+ levels G OR 0.23 1E-74 PubMed

Sources