Sensitive

14-3-3 protein theta level in Chronic kidney disease with hypertension and no diabetes (7625_27)

VTN · rs2227723

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 1.34-2.24); p = 8 × 10−15.

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

Where it sits Chromosome 17, band 17q11.2 — a missense change in VTN.

What ClinVar records

Classification Benign for VTN-related disorder; no assertion criteria provided (0 of 4 stars, 1 submitter), last evaluated 2019-11-25. ClinVar record 3041993 NM_000638.4(VTN):c.803G>A (p.Arg268Gln)

What this is ClinVar's aggregate record for this position (as of its 2026-10-12 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 14-3-3 protein theta level in Chronic kidney disease with hypertension and no diabetes (7625_27). This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to 14-3-3 protein theta level in Chronic kidney disease with hypertension and no diabetes (7625_27). That is a smaller link than two copies.
T/T Two copies of the version the research linked to 14-3-3 protein theta level in Chronic kidney disease with hypertension and no diabetes (7625_27). That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs2227723

What is rs2227723?

rs2227723 is a single position in the genome, in or near the VTN gene. Published research associates it with 14-3-3 protein theta level in chronic kidney disease with hypertension and no diabetes (7625_27). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs2227723 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 rs2227723 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

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14-3-3 protein theta level in Chronic kidney disease with hypertension and no diabetes (7625_27) (rs2227723). MyGeneLog™. https://www.mygenelog.com/variants/rs2227723

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