Standard

mean corpuscular hemoglobin (MCH, maximum, inv-norm transformed)

SERPING1 · rs146802501

What the study found

Who was studied 114,852 African American or Afro-Caribbean individuals, 55,783 Hispanic or Latin American individuals, 5,942 East Asian ancestry individuals, 407,288 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0325 higher (95% confidence interval 0.025-0.04); p = 1 × 10−16.

How common The A allele had a frequency of about 78% in the people studied.

Where it sits Chromosome 11, band 11q12.1 — in an intron of SERPING1.

What each result means

A/A Two copies of the version the research linked to mean corpuscular hemoglobin (MCH, maximum, inv-norm transformed). That is the strongest link of the three results. A link in a study is not a diagnosis.
A/C One copy of the version the research linked to mean corpuscular hemoglobin (MCH, maximum, inv-norm transformed). That is a smaller link than two copies.
C/C No copy of the version the research linked to mean corpuscular hemoglobin (MCH, maximum, inv-norm transformed). This is the starting point the study compared everyone against.
Source

Questions about rs146802501

What is rs146802501?

rs146802501 is a single position in the genome, in or near the SERPING1 gene. Published research associates it with mean corpuscular hemoglobin (mch, maximum, inv-norm transformed). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs146802501 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 rs146802501 come from?

GWAS Catalog, Science (New York, N.Y.) 2024, PMID:39024449. 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.

mean corpuscular hemoglobin (MCH, maximum, inv-norm transformed) (rs146802501). MyGeneLog™. https://www.mygenelog.com/variants/rs146802501

← See all variants