Variants linked to Blood Pressure

Continuously updated · newest added Oct 23, 2026

2,151 positions on this site are linked to Blood Pressure, out of 109,880 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

near TRIM36 · rs200678820

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Diastolic blood pressure

near DIP2B · rs55696064

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Diastolic blood pressure (MTAG)

near RNU5E-1 · rs4529715

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Systolic blood pressure (UKB data field 4080)

LINC02625 · rs7070797

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Diastolic blood pressure

MAP4 · rs777017

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Systolic blood pressure

HOTTIP · rs2071265

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Diastolic blood pressure (MTAG)

MECOM · rs2242338

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Systolic blood pressure

GUCY1A1 · rs12643599

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Diastolic blood pressure

SPI1 · rs896817

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Diastolic blood pressure (MTAG)

LINC02580 · rs10167379

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Diastolic blood pressure (MTAG)

near UBA52P7 · rs10850526

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Systolic blood pressure (MTAG)

PRDM6 · rs6890251

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Diastolic blood pressure (MTAG)

ATP2B1-AS1 · rs11105429

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Standard

Systolic blood pressure (MTAG)

near RNU5E-1 · rs12726853

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Systolic blood pressure

INSR · rs75392157

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Standard

Systolic blood pressure (MTAG)

near MARK2P11 · rs1957563

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Diastolic blood pressure

PPCDC · rs12148555

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Diastolic blood pressure

near GUCY1A1 · rs112179314

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Diastolic blood pressure (MTAG)

near LINC00322 · rs60376124

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

near RXFP2 · rs12876275

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Showing 20 of 2151 · page 39 of 108

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.