Variants linked to Blood Pressure

Continuously updated · newest added Oct 22, 2026

2,108 positions on this site are linked to Blood Pressure, out of 108,284 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

← Back to Blood Pressure

Standard

Systolic blood pressure (MTAG)

TMEM26-AS1 · rs2787724

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Standard

Diastolic blood pressure

near MTND1P22 · rs2138741

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Standard

Diastolic blood pressure (MTAG)

MPI · rs139190144

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Standard

Systolic blood pressure

near LINC00639 · rs12895569

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Standard

Diastolic blood pressure

PALM2AKAP2 · rs10980141

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Standard

Systolic blood pressure (MTAG)

VCL · rs10824058

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Standard

Systolic blood pressure (MTAG)

GIT2 · rs9634314

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Standard

Systolic blood pressure

ATP2B1-AS1 · rs7313782

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Standard

Diastolic blood pressure (MTAG)

SLX4IP · rs73075324

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Standard

Systolic blood pressure

EEPD1 · rs62447769

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Standard

Diastolic blood pressure (MTAG)

LTBP4 · rs62107907

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Standard

Systolic blood pressure (MTAG)

MCTS2 · rs6058088

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Standard

Systolic blood pressure

LINC02227 · rs4490571

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Standard

Diastolic blood pressure (MTAG)

STEAP2-AS1 · rs39281

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Standard

Diastolic blood pressure

NUFIP2 · rs16964955

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Standard

Systolic blood pressure (MTAG)

NEURL1-AS1 · rs138286588

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Standard

Systolic blood pressure

SIK3 · rs1320668

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Standard

Diastolic blood pressure

ANKFY1 · rs12943517

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Standard

systolic blood pressure (SBP, mean, inv-normal transformed)

TNS2-AS1 · rs12368584

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Standard

systolic blood pressure (SBP, mean, inv-normal transformed)

ESR1 · rs111762276

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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.