Sensitive
Myocardial infarction
APOC1 · rs56131196
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 (two copies of the reported risk allele) with a higher likelihood of Myocardial infarction compared to the general population.
A/G
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Myocardial infarction.
G/G
Published research associates this genotype with typical/baseline likelihood of Myocardial infarction — no copies of the reported risk allele.
Source
A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease
Nikpay M,
Goel A,
Won HH,
Hall LM,
Willenborg C,
Kanoni S,
Saleheen D,
Kyriakou T,
Nelson CP,
Hopewell JC,
Webb TR,
Zeng L
and 139 more — show all
Dehghan A,
Alver M,
Armasu SM,
Auro K,
Bjonnes A,
Chasman DI,
Chen S,
Ford I,
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Grace C,
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Huang J,
Hwang SJ,
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Lu X,
Lu Y,
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Morrison AC,
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Qu L,
Rose LM,
Salfati E,
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Scholz M,
Smith AV,
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Uitterlinden A,
Yang X,
Zhang W,
Zhao W,
de Andrade M,
de Vries PS,
van Zuydam NR,
Anand SS,
Bertram L,
Beutner F,
Dedoussis G,
Frossard P,
Gauguier D,
Goodall AH,
Gottesman O,
Haber M,
Han BG,
Huang J,
Jalilzadeh S,
Kessler T,
König IR,
Lannfelt L,
Lieb W,
Lind L,
Lindgren CM,
Lokki ML,
Magnusson PK,
Mallick NH,
Mehra N,
Meitinger T,
Memon FU,
Morris AP,
Nieminen MS,
Pedersen NL,
Peters A,
Rallidis LS,
Rasheed A,
Samuel M,
Shah SH,
Sinisalo J,
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Wang L,
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Ardissino D,
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Danesh J,
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Elosua R,
Epstein SE,
Esko T,
Feitosa MF,
Franco OH,
Franzosi MG,
Granger CB,
Gu D,
Gudnason V,
Hall AS,
Hamsten A,
Harris TB,
Hazen SL,
Hengstenberg C,
Hofman A,
Ingelsson E,
Iribarren C,
Jukema JW,
Karhunen PJ,
Kim BJ,
Kooner JS,
Kullo IJ,
Lehtimäki T,
Loos RJF,
Melander O,
Metspalu A,
März W,
Palmer CN,
Perola M,
Quertermous T,
Rader DJ,
Ridker PM,
Ripatti S,
Roberts R,
Salomaa V,
Sanghera DK,
Schwartz SM,
Seedorf U,
Stewart AF,
Stott DJ,
Thiery J,
Zalloua PA,
O'Donnell CJ,
Reilly MP,
Assimes TL,
Thompson JR,
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Clarke R,
Watkins H,
Kathiresan S,
McPherson R,
Deloukas P,
Schunkert H,
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Nature genetics · 2015 · PMID 26343387 · open access
Questions about rs56131196
What is rs56131196?
rs56131196 is a single position in the genome, in or near the APOC1 gene. Published research associates it with myocardial infarction. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs56131196 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 rs56131196 come from?
GWAS Catalog, Nat Genet 2015, PMID:26343387. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants