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End-stage coagulation

CFHR4 · rs10922162

Where this position leads

Condition: Fibrinogen and Blood Clotting

rs10922162 Condition: Fibrinogen and Blood Clotting Fibrinogen and Blood Clotting Condition rs10922162 rs10922162 CFHR4

What the study found

Who was studied 2,100 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.521 higher (95% confidence interval 0.43-0.61); p = 2 × 10−30.

How common The C allele had a frequency of about 84% in the people studied.

Where it sits Chromosome 1, band 1q31.3 — a synonymous change in ASPM.

What ClinVar records

Classification Benign for Microcephaly 5, primary, autosomal recessive, Familial cancer of breast; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 13 submitters), last evaluated 2026-02-03. ClinVar record 21603 NM_018136.5(ASPM):c.7605G>A (p.Val2535=)

What this is ClinVar's aggregate record for this position (as of its 2026-10-19 release), not a result about you. A classification describes the variant against the condition named, as laboratories submitted it. Whether a person carries this variant, and what that would mean for them, is a question for a clinical test and a genetic counsellor.

What each result means

C/C Two copies of the version the research linked to End-stage coagulation. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/T One copy of the version the research linked to End-stage coagulation. That is a smaller link than two copies.
T/T No copy of the version the research linked to End-stage coagulation. This is the starting point the study compared everyone against.
Source

Questions about rs10922162

What is rs10922162?

rs10922162 is a single position in the genome, in or near the CFHR4 gene. Published research associates it with end-stage coagulation. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs10922162 linked to?

On MyGeneLog this position is linked to Fibrinogen and Blood Clotting. The research behind each link, and its sources, are set out on that condition page.

Does having rs10922162 mean I will get this?

No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.

Where does the information about rs10922162 come from?

GWAS Catalog, Ann Neurol 2013, PMID:23381943. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

End-stage coagulation (rs10922162). MyGeneLog™. https://www.mygenelog.com/variants/rs10922162

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