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Sensitive

Depression

near TMEM97P2 · rs7017108

Where this position leads

Condition: Endometriosis and Depression: Shared Genetics

rs7017108 Condition: Endometriosis and Depression: Shared Genetics Endometriosis and Depression: Share… Condition rs7017108 rs7017108 near TMEM97P2

What the study found

Who was studied 371,184 European ancestry cases, 978,703 European ancestry controls.

The effect Each copy of the C allele shifted the measure 0.0178 lower (95% confidence interval 0.012-0.023); p = 2 × 10−10.

How common The C allele had a frequency of about 57% in the people studied.

Where it sits Chromosome 8, band 8p21.3 — between genes, 19.6 kb from TMEM97P2.

What each result means

C/C Two copies of the version the research linked to Depression. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/T One copy of the version the research linked to Depression. That is a smaller link than two copies.
T/T No copy of the version the research linked to Depression. This is the starting point the study compared everyone against.
Source
Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses
Als TD, Kurki MI, Grove J, Voloudakis G, Therrien K, Tasanko E, Nielsen TT, Naamanka J, Veerapen K, Levey DF, Bendl J, Bybjerg-Grauholm J
and 31 more — show all
Zeng B, Demontis D, Rosengren A, Athanasiadis G, Bækved-Hansen M, Qvist P, Bragi Walters G, Thorgeirsson T, Stefánsson H, Musliner KL, Rajagopal VM, Farajzadeh L, Thirstrup J, Vilhjálmsson BJ, McGrath JJ, Mattheisen M, Meier S, Agerbo E, Stefánsson K, Nordentoft M, Werge T, Hougaard DM, Mortensen PB, Stein MB, Gelernter J, Hovatta I, Roussos P, Daly MJ, Mors O, Palotie A, Børglum AD
Nature medicine · 2023 · PMID 37464041

Questions about rs7017108

What is rs7017108?

rs7017108 is a single position in the genome, in or near the near TMEM97P2 gene. Published research associates it with depression. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs7017108 linked to?

On MyGeneLog this position is linked to Endometriosis and Depression: Shared Genetics. The research behind each link, and its sources, are set out on that condition page.

Does having rs7017108 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 rs7017108 come from?

GWAS Catalog, Nature medicine 2023, PMID:37464041. 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.

Depression (rs7017108). MyGeneLog™. https://www.mygenelog.com/variants/rs7017108

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