Variants linked to Blood Pressure

Continuously updated · newest added Oct 23, 2026

2,162 positions on this site are linked to Blood Pressure, out of 110,511 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

ARHGAP27 · rs76344126

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Standard

Systolic blood pressure

PTRH1 · rs117595338

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Standard

Diastolic blood pressure

TARID · rs10872410

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Standard

Diastolic blood pressure

H2BC4 · rs74571768

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Standard

Systolic blood pressure

near RPS11P1 · rs6078093

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Standard

Diastolic blood pressure

PITPNM3 · rs2009598

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Standard

Systolic blood pressure

IER5L-AS1 · rs184457

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Standard

Systolic blood pressure

CCDC170 · rs12199746

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Standard

Systolic blood pressure (MTAG)

BCAS3 · rs9652858

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Standard

Diastolic blood pressure

SLC7A2 · rs75902664

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Standard

Systolic blood pressure (standard GWA)

LINC02576 · rs7559813

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Standard

Diastolic blood pressure (MTAG)

FOSL2 · rs6547850

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Standard

Diastolic blood pressure

near TRIM77BP · rs2078134

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Standard

Systolic blood pressure (MTAG)

near AHDC1 · rs17361679

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Standard

Systolic blood pressure

near MIR6078 · rs10508275

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Standard

Systolic blood pressure

SH3TC2 · rs4705298

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Standard

Diastolic blood pressure

ADM-DT · rs3814700

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Standard

Diastolic blood pressure

EXD3 · rs28374197

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Standard

Systolic blood pressure

SETBP1 · rs2615000

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Standard

Systolic blood pressure

DCAF12-AS1 · rs12552937

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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.