Standard
Serum parathyroid hormone levels
SLC34A1 · rs4074995
Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What each result means
A/A
Published research associates this genotype with typical/baseline likelihood of Serum parathyroid hormone levels — no copies of the reported risk allele.
A/G
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Serum parathyroid hormone levels.
G/G
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Serum parathyroid hormone levels compared to the general population.
Source
Genetic Variants Associated with Circulating Parathyroid Hormone
Robinson-Cohen C,
Lutsey PL,
Kleber ME,
Nielson CM,
Mitchell BD,
Bis JC,
Eny KM,
Portas L,
Eriksson J,
Lorentzon M,
Koller DL,
Milaneschi Y
and 37 more — show all
Teumer A,
Pilz S,
Nethander M,
Selvin E,
Tang W,
Weng LC,
Wong HS,
Lai D,
Peacock M,
Hannemann A,
Völker U,
Homuth G,
Nauk M,
Murgia F,
Pattee JW,
Orwoll E,
Zmuda JM,
Riancho JA,
Wolf M,
Williams F,
Penninx B,
Econs MJ,
Ryan KA,
Ohlsson C,
Paterson AD,
Psaty BM,
Siscovick DS,
Rotter JI,
Pirastu M,
Streeten E,
März W,
Fox C,
Coresh J,
Wallaschofski H,
Pankow JS,
de Boer IH,
Kestenbaum B
Journal of the American Society of Nephrology : JASN · 2017 · PMID 27927781
Questions about rs4074995
What is rs4074995?
rs4074995 is a single position in the genome, in or near the SLC34A1 gene. Published research associates it with serum parathyroid hormone levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs4074995 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 rs4074995 come from?
GWAS Catalog, J Am Soc Nephrol 2016, PMID:27927781. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants