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

Systolic blood pressure (MTAG)

GUCY1B1 · rs78975989

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Standard

Diastolic blood pressure (MTAG)

near NPR3 · rs7713318

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Standard

Diastolic blood pressure

PTPN11 · rs75326242

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Standard

Diastolic blood pressure (MTAG)

IGF2BP2 · rs73175562

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Standard

Diastolic blood pressure (MTAG)

near HRCT1 · rs7043204

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Standard

Diastolic blood pressure (MTAG)

near LINC02227 · rs62384984

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Standard

Systolic blood pressure (MTAG)

TCF7L2 · rs61872795

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Standard

Diastolic blood pressure

near YWHAQ · rs57503539

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Standard

Diastolic blood pressure (MTAG)

BSN-DT · rs34519883

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Standard

Diastolic blood pressure

CCNE1 · rs34331990

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Standard

Diastolic blood pressure

PODXL · rs1733860

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Standard

Diastolic blood pressure (MTAG)

near VGLL2 · rs1534217

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Standard

Diastolic blood pressure (MTAG)

ATP2B1 · rs149731397

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Standard

Diastolic blood pressure

LINC01400 · rs13297152

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Systolic blood pressure

SOX6 · rs12798653

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Standard

Systolic blood pressure

HSD17B12 · rs11606658

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Systolic blood pressure

near KCNK17 · rs115537302

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Systolic blood pressure

GRIN2B · rs1030056

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Systolic blood pressure

PRDM6 · rs10077410

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Standard

Diastolic blood pressure (MTAG)

ESR1 · rs9478282

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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.