Variants linked to Blood Pressure

Continuously updated · newest added Oct 22, 2026

2,105 positions on this site are linked to Blood Pressure, out of 108,158 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

FRYL · rs13108799

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Standard

Diastolic blood pressure (MTAG)

near CCNE1 · rs11084240

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Standard

Diastolic blood pressure

SBF2 · rs61877008

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Standard

Diastolic blood pressure

TTN · rs56207956

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Standard

Systolic blood pressure (MTAG)

near LINC02151 · rs4938229

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Standard

Systolic blood pressure

near PRPS1P1 · rs418085

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Standard

Systolic blood pressure (standard GWA)

PRDM6 · rs337125

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Standard

Systolic blood pressure

GOSR2-DT · rs197913

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Standard

Systolic blood pressure (MTAG)

RSRC1 · rs17684859

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Standard

Systolic blood pressure

PLEKHG1 · rs12664595

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Standard

Systolic blood pressure

ARHGAP42 · rs10895022

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Standard

Diastolic blood pressure (MTAG)

MYL2 · rs78887867

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Standard

Systolic blood pressure

ZFPM2-AS1 · rs7003445

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Standard

Systolic blood pressure

near IPO11 · rs35807464

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Standard

Systolic blood pressure (MTAG)

ASMER1 · rs1297213

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Standard

Diastolic blood pressure (MTAG)

AEBP2 · rs10841225

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Standard

Diastolic blood pressure (MTAG)

near HNRNPA1P73 · rs10245801

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Standard

Diastolic blood pressure

LINC02428 · rs7695593

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Standard

Systolic blood pressure

KDM2B · rs57917116

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Standard

Systolic blood pressure

POC1B-AS1 · rs4842667

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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.