Sensitive

Kremen protein 1 level in Chronic kidney disease with hypertension and no diabetes (17331_138)

KREMEN1 · rs61752343

What the study found

Who was studied 466 African American individuals.

The effect Each copy of the T allele shifted the measure 1.79 lower (95% confidence interval 1.28-2.3); p = 2 × 10−12.

How common The T allele had a frequency of about 2% in the people studied.

Where it sits Chromosome 22, band 22q12.1 — a missense change in KREMEN1.

What ClinVar records

Classification Benign; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 2 submitters), last evaluated 2026-02-02. ClinVar record 712873 NM_001039570.3(KREMEN1):c.739C>T (p.Arg247Trp)

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 No copy of the version the research linked to Kremen protein 1 level in Chronic kidney disease with hypertension and no diabetes (17331_138). This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Kremen protein 1 level in Chronic kidney disease with hypertension and no diabetes (17331_138). That is a smaller link than two copies.
T/T Two copies of the version the research linked to Kremen protein 1 level in Chronic kidney disease with hypertension and no diabetes (17331_138). That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs61752343

What is rs61752343?

rs61752343 is a single position in the genome, in or near the KREMEN1 gene. Published research associates it with kremen protein 1 level in chronic kidney disease with hypertension and no diabetes (17331_138). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs61752343 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 rs61752343 come from?

GWAS Catalog, Kidney international 2022, PMID:35870639. 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.

Kremen protein 1 level in Chronic kidney disease with hypertension and no diabetes (17331_138) (rs61752343). MyGeneLog™. https://www.mygenelog.com/variants/rs61752343

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