Variants linked to Blood Pressure

Continuously updated · newest added Oct 23, 2026

2,188 positions on this site are linked to Blood Pressure, out of 112,191 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

UNC13D · rs3744010

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Standard

Diastolic blood pressure (MTAG)

near ADRB1 · rs17875473

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Standard

Diastolic blood pressure

near CDKN2C · rs116287796

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Standard

Systolic blood pressure (MTAG)

near AP5B1 · rs112437639

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Standard

Diastolic blood pressure (MTAG)

CMIP · rs62046629

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Standard

Diastolic blood pressure

near KRT18P16 · rs17150778

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Systolic blood pressure (MTAG)

NPPA · rs17376426

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Standard

Systolic blood pressure (MTAG)

near FBN2 · rs17676242

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Standard

Systolic blood pressure

ADCY3 · rs80195592

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Standard

Systolic blood pressure

ZFPM2 · rs71506363

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High blood pressure / hypertension

CACNA1D · rs3821845

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Standard

Diastolic blood pressure

TNS1 · rs1035673

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Systolic blood pressure

MYO9B · rs3745348

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Systolic blood pressure

LINC02201 · rs34039004

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Standard

Diastolic blood pressure

VARS · rs3130491

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Standard

Systolic blood pressure (MTAG)

ATP2B1-AS1 · rs112591226

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Systolic blood pressure

IK · rs778593

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diastolic blood pressure (DBP, mean, inv-normal transformed)

near VPS25 · rs111982267

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Diastolic blood pressure

ARHGEF26 · rs73158427

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Standard

Systolic blood pressure

near LINC02620 · rs7076147

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Showing 20 of 2188 · page 54 of 110

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.