Genetic variant

rs1671152

rs1671152 is a single-letter difference in human DNA, on chromosome 19. 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 rs1671152 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 rs1671152, 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
rs1671152
Position
chr19:55014977

Genome-wide association studies (20)

TraitRisk alleleOR / betaP-valueStudy
MMP1 protein levels G β 0.095 2E-48 PubMed
BGN protein levels G β 0.096 1E-38 PubMed
CCL14 protein levels G β 0.084 5E-33 PubMed
CXCL8 protein levels G β 0.09 4E-32 PubMed
CCL2 protein levels G β 0.083 4E-27 PubMed
MPIG6B protein levels G β 0.084 1E-25 PubMed
F2R protein levels G β 0.071 1E-19 PubMed
JAM3 protein levels G β 0.071 2E-19 PubMed
Platelet side scatter distribution width G β 0.096 5E-18 PubMed
PLXNA4 protein levels G β 0.065 5E-16 PubMed
NAA80 protein levels G β 0.064 7E-15 PubMed
CHMP1A protein levels G β 0.065 8E-15 PubMed
RAB27B protein levels G β 0.064 8E-15 PubMed
DUT protein levels G β 0.061 4E-14 PubMed
DECR1 protein levels G β 0.062 7E-14 PubMed
Platelet aggregation T — 8E-14 PubMed
NFU1 protein levels G β 0.06 8E-14 PubMed
BCL2L1 protein levels G β 0.062 9E-14 PubMed
NRGN protein levels G β 0.061 1E-13 PubMed
THTPA protein levels G β 0.06 1E-13 PubMed

Sources