Standard
Serum 25-Hydroxyvitamin D levels
ANO6/ARID2 · rs719700
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
C/C
Published research associates this genotype with typical/baseline likelihood of Serum 25-Hydroxyvitamin D 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 Serum 25-Hydroxyvitamin D levels.
T/T
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Serum 25-Hydroxyvitamin D levels compared to the general population.
Source
Transethnic Evaluation Identifies Low-Frequency Loci Associated With 25-Hydroxyvitamin D Concentrations
Hong J,
Hatchell KE,
Bradfield JP,
Bjonnes A,
Chesi A,
Lai CQ,
Langefeld CD,
Lu L,
Lu Y,
Lutsey PL,
Musani SK,
Nalls MA
and 48 more — show all
Robinson-Cohen C,
Roizen JD,
Saxena R,
Tucker KL,
Ziegler JT,
Arking DE,
Bis JC,
Boerwinkle E,
Bottinger EP,
Bowden DW,
Gilsanz V,
Houston DK,
Kalkwarf HJ,
Kelly A,
Lappe JM,
Liu Y,
Michos ED,
Oberfield SE,
Palmer ND,
Rotter JI,
Sapkota B,
Shepherd JA,
Wilson JG,
Basu S,
de Boer IH,
Divers J,
Freedman BI,
Grant SFA,
Hakanarson H,
Harris TB,
Kestenbaum BR,
Kritchevsky SB,
Loos RJF,
Norris JM,
Norwood AF,
Ordovas JM,
Pankow JS,
Psaty BM,
Sanghera DK,
Wagenknecht LE,
Zemel BS,
Meigs J,
Dupuis J,
Florez JC,
Wang T,
Liu CT,
Engelman CD,
Billings LK
The Journal of clinical endocrinology and metabolism · 2018 · PMID 29325163
Questions about rs719700
What is rs719700?
rs719700 is a single position in the genome, in or near the ANO6/ARID2 gene. Published research associates it with serum 25-hydroxyvitamin d levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs719700 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 rs719700 come from?
GWAS Catalog, J Clin Endocrinol Metab 2018, PMID:29325163. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants