Variants linked to Myocardial Infarction

Continuously updated · newest added Oct 10, 2026

14 positions on this site are linked to Myocardial Infarction, out of 61,148 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

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Sensitive

Myocardial infarction

near HLA-B · rs117598591

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Sensitive

Myocardial infarction

HHIPL1 · rs12897285

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Sensitive

Myocardial infarction

IL6R · rs6694258

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Sensitive

Myocardial infarction

HHIPL1 · rs9788497

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Sensitive

Myocardial infarction

BORCS7-ASMT · rs11191447

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Sensitive

Myocardial infarction

FLT1 · rs77330370

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Sensitive

Myocardial infarction

LPA · rs932631509

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Sensitive

Myocardial infarction

near EDNRA · rs72957606

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Sensitive

Myocardial infarction

EDNRA · rs17612742

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Sensitive

Myocardial infarction

GUCY1A3 · rs72689147

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Sensitive

Myocardial infarction

APOC1 · rs56131196

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Sensitive

Myocardial infarction

CXCL12 · rs1870634

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Sensitive

Myocardial infarction

9p21 · rs2891168

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Sensitive

Incident myocardial infarction

QKI · rs6941513

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Questions about variants on this site

What is a "variant" page on this site?

One specific position in the genome (an rsID), explained in plain language with what published research has found it linked to, and how strong that link actually is.

Where does new variant data come from?

The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.

Does being listed here mean a variant causes a condition?

No. Listing reflects an association from published research, not a diagnosis or a cause. Most common variants shift probability modestly rather than determining an outcome.

Can I search this list by gene or rsID?

Yes — the search box above matches gene symbols and rsIDs as well as trait names.