Genetic variant

rs10801555

rs10801555 is a single-letter difference in human DNA, on chromosome 1. 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 rs10801555 is the catalogue number of one of them. Which letters you carry there — one copy from each parent — is your genotype.

We hold only the basic reference record for this variant: its ID and position. Many catalogued variants have never been linked to anything.

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 rs10801555, 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
rs10801555
Position
chr1:196691131

Genome-wide association studies (20)

TraitRisk alleleOR / betaP-valueStudy
Angiopoietin-related protein 1 levels A OR 0.23 5E-56 PubMed
Age-related macular degeneration A OR 2.33 2E-47 PubMed
Zinc fingers and homeoboxes protein 3 levels A OR 0.2 6E-46 PubMed
Matrix metalloproteinase-17 levels A OR 0.18 9E-38 PubMed
Proteasome subunit alpha type-3 levels A OR 0.18 5E-35 PubMed
Heparan sulfate glucosamine 3-O-sulfotransferase 1 levels A OR 0.18 8E-35 PubMed
HEPACAM family member 2 levels A OR 0.17 2E-32 PubMed
Carbonic anhydrase 12 levels A OR 0.17 6E-31 PubMed
Carcinoembryonic antigen-related cell adhesion molecule 21 levels A OR 0.16 2E-29 PubMed
ADP-ribosylation factor-like protein 9 levels A OR 0.16 2E-27 PubMed
Fibroblast growth factor 10 levels A OR 0.16 3E-27 PubMed
Histone acetyltransferase KAT2A levels A OR 0.16 5E-27 PubMed
Fibulin-5 levels A OR 0.15 9E-26 PubMed
Age-related macular degeneration A OR 0.21 1E-25 PubMed
Prostate and testis expressed protein 1 levels A OR 0.15 2E-25 PubMed
Leucine-rich repeat, immunoglobulin-like domain and transmembrane domain-containing protein 2 levels A OR 0.15 7E-24 PubMed
Phosphomevalonate kinase level in Chronic kidney disease with hypertension and no diabetes (12450_42) G OR 0.62 2E-23 PubMed
cAMP-regulated phosphoprotein 19 levels A OR 0.14 2E-23 PubMed
Tenascin-R levels A OR 0.14 2E-23 PubMed
Caspase-2 levels A OR 0.14 5E-23 PubMed

Sources