Variants linked to Blood Pressure

Continuously updated · newest added Oct 22, 2026

2,097 positions on this site are linked to Blood Pressure, out of 107,684 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 (MTAG)

PRDM16 · rs75063997

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Standard

Diastolic blood pressure (MTAG)

CADM2 · rs62263915

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Standard

Diastolic blood pressure

ZFAT · rs4909609

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Standard

Systolic blood pressure (MTAG)

HIBADH · rs2391449

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Standard

Systolic blood pressure (MTAG)

MKX-AS1 · rs2246842

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Standard

Diastolic blood pressure (MTAG)

near PRDM8 · rs17465728

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Diastolic blood pressure (MTAG)

ZDHHC18 · rs17162311

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Standard

Diastolic blood pressure

FAM208A · rs9845655

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Standard

Diastolic blood pressure

near PACRG-AS1 · rs9365555

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Standard

Systolic blood pressure

FHL1 · rs926905

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Standard

Diastolic blood pressure

near ZNF629 · rs8058961

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Standard

Diastolic blood pressure (MTAG)

GIPC2 · rs7540686

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Standard

Diastolic blood pressure

near TANC2 · rs7217129

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Standard

Diastolic blood pressure (MTAG)

near LINC01679 · rs644931

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Standard

Systolic blood pressure (MTAG)

LINC02227 · rs62386478

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Standard

Diastolic blood pressure

LINC01376 · rs55878177

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Standard

Diastolic blood pressure (MTAG)

IPO9-AS1 · rs3001023

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Systolic blood pressure

LINC02210-CRHR1 · rs241033

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Standard

Systolic blood pressure (MTAG)

CACNA1C · rs2239046

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Standard

Systolic blood pressure

ATP2B1-AS1 · rs12824962

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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.