Variants linked to Blood Pressure

Continuously updated · newest added Oct 22, 2026

2,098 positions on this site are linked to Blood Pressure, out of 107,852 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

Diastolic blood pressure

near EDEM3 · rs9425339

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Standard

Diastolic blood pressure

PRANCR · rs80222951

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Standard

Systolic blood pressure

near RNY1P8 · rs79944483

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Standard

Diastolic blood pressure

SLC25A37 · rs7842144

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Standard

Systolic blood pressure

ERO1A · rs78058068

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Standard

Diastolic blood pressure

near NPR3 · rs72740613

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Standard

Diastolic blood pressure (MTAG)

EMSY · rs7115331

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Standard

Diastolic blood pressure (MTAG)

KCNK5 · rs6918122

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Standard

Diastolic blood pressure (MTAG)

near BET1P1 · rs66743416

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Standard

Systolic blood pressure

CARMIL1 · rs55946641

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Standard

Systolic blood pressure

near RPS4XP9 · rs55815739

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Standard

Systolic blood pressure

near ADAM11 · rs4793146

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Standard

Diastolic blood pressure

ARHGAP42 · rs4754697

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Standard

Diastolic blood pressure

ERG · rs2836554

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Standard

Diastolic blood pressure

HOXB3 · rs2740753

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Standard

Systolic blood pressure

LCORL · rs2724485

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Standard

Diastolic blood pressure (MTAG)

MECOM · rs2421747

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Standard

Diastolic blood pressure (MTAG)

DDI2 · rs1980607

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Standard

Diastolic blood pressure (MTAG)

near FRK · rs195486

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Standard

Diastolic blood pressure

BRAP · rs187459270

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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.