Genetic variant

rs2274224

rs2274224 is a single-letter difference in human DNA, on chromosome 10. 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 rs2274224 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 rs2274224, 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
rs2274224
Position
chr10:94279840

Genome-wide association studies (20)

TraitRisk alleleOR / betaP-valueStudy
Diastolic blood pressure C OR 0.25 2E-62 PubMed
Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node12) — OR 0.11 9E-53 PubMed
Systolic blood pressure C OR 0.36 5E-50 PubMed
Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net25_Node3) — OR 0.11 2E-47 PubMed
Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net25_Node21) — OR 0.1 2E-42 PubMed
Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node25) — OR 0.1 4E-42 PubMed
Diastolic blood pressure C OR 0.27 3E-39 PubMed
Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node42) — β 0.092 1E-37 PubMed
Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node17) — β 0.089 2E-36 PubMed
Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node24) — β 0.09 6E-36 PubMed
Systolic blood pressure C OR 0.44 2E-34 PubMed
Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node49) — β 0.081 2E-30 PubMed
Body fat percentage G β 0.017 7E-29 PubMed
Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node46) — β 0.079 2E-28 PubMed
Metabolic biomarkers (multivariate analysis) G — 3E-28 PubMed
systolic blood pressure (SBP, mean, inv-normal transformed) G β 0.027 9E-28 PubMed
White blood cell count C — 2E-27 PubMed
systolic blood pressure (SBP, maximum, inv-normal transformed) G β 0.026 2E-27 PubMed
Migraine G OR 1.06 3E-26 PubMed
systolic blood pressure (SBP, mean, inv-normal transformed) G β 0.026 4E-24 PubMed

Sources