Variants linked to Blood Pressure

Continuously updated · newest added Oct 22, 2026

2,076 positions on this site are linked to Blood Pressure, out of 106,844 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

SLC22A14 · rs11129785

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Diastolic blood pressure (MTAG)

MIX23 · rs9863881

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Systolic blood pressure (MTAG)

SBF2 · rs7928572

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Standard

Systolic blood pressure (MTAG)

near SLC45A4 · rs79119657

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Standard

Systolic blood pressure (MTAG)

LSP1 · rs78405116

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Systolic blood pressure (MTAG)

TEX41 · rs62167178

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Diastolic blood pressure

ADRA1A · rs58623861

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Standard

Diastolic blood pressure (MTAG)

near MRPS31P1 · rs4974072

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Standard

Systolic blood pressure (MTAG)

MEF2C-AS1 · rs28690315

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Standard

Systolic blood pressure (MTAG)

ARL15 · rs255761

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Standard

Systolic blood pressure

CACNA1C · rs2283294

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Standard

Diastolic blood pressure (MTAG)

NGF-AS1 · rs2057125

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Standard

Diastolic blood pressure (MTAG)

TP53 · rs12949655

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Standard

Systolic blood pressure (MTAG)

near DNAJC8P1 · rs12147633

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Systolic blood pressure (MTAG)

PSMD7-DT · rs12103229

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Standard

Diastolic blood pressure

CDH13 · rs11640600

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Systolic blood pressure

HNF1A · rs11065381

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Systolic blood pressure

CFAP92 · rs10512711

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Diastolic blood pressure (MTAG)

SLX4IP · rs78896696

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Systolic blood pressure

near SPATA7 · rs7160184

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Showing 20 of 2076 · page 1 of 104

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.