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Creatinine levels

SLC34A1 · rs3812036

Where this position leads

What the study found

Who was studied 16,347 British ancestry from 6863 families..

The effect Each copy of the T allele shifted the measure 0.0928 mg/dl higher (95% confidence interval 0.065-0.121); p = 1 × 10⁻¹⁰.

How common The T allele had a frequency of about 23% in the people studied.

Where it sits Chromosome 5, band 5q35.3 — in an intron of SLC34A1.

What ClinVar records

Classification Benign for Hypercalcemia, infantile, 2, Fanconi renotubular syndrome 2, Hypophosphatemic nephrolithiasis/osteoporosis 1; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 7 submitters), last evaluated 2026-02-04. ClinVar record 1168138 NM_003052.5(SLC34A1):c.389-20C>T

What this is ClinVar's aggregate record for this position (as of its 2026-10-05 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 Published research associates this genotype with typical/baseline likelihood of Creatinine levels — no copies of the reported risk allele.

C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Creatinine levels.

T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Creatinine levels compared to the general population.

Source

Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants

Nagy R, Boutin TS, Marten J, Huffman JE, Kerr SM, Campbell A, Evenden L, Gibson J, Amador C, Howard DM, Navarro P, Morris A

and 13 more — show all

Deary IJ, Hocking LJ, Padmanabhan S, Smith BH, Joshi P, Wilson JF, Hastie ND, Wright AF, McIntosh AM, Porteous DJ, Haley CS, Vitart V, Hayward C

Genome medicine · 2017 · PMID 28270201 · open access

Questions about rs3812036

What is rs3812036?

rs3812036 is a single position in the genome, in or near the SLC34A1 gene. Published research associates it with creatinine levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs3812036 linked to?

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

Does having rs3812036 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 rs3812036 come from?

GWAS Catalog, Genome Med 2017, PMID:28270201. 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.

Creatinine levels (rs3812036). MyGeneLog™. https://www.mygenelog.com/variants/rs3812036

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