Variants linked to Blood Pressure

Continuously updated · newest added Oct 23, 2026

2,179 positions on this site are linked to Blood Pressure, out of 111,435 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

REN · rs72749713

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Standard

Systolic blood pressure

SKAP1 · rs62064990

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Standard

Diastolic blood pressure

BICC1 · rs4948550

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Standard

Diastolic blood pressure

near RNU4-35P · rs76785130

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Standard

Systolic blood pressure (MTAG)

near LINC02620 · rs7081664

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Standard

Diastolic blood pressure (MTAG)

near CHST12 · rs56145652

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Standard

Systolic blood pressure

near PDP2 · rs3843712

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Standard

Diastolic blood pressure (MTAG)

ARHGEF3 · rs34873381

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Standard

Systolic blood pressure

near LINC02229 · rs3121685

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Standard

Diastolic blood pressure

ARAP2 · rs1878825

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Standard

Diastolic blood pressure

SOX13 · rs16852778

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Standard

Systolic blood pressure

SBF2 · rs139275268

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Standard

Systolic blood pressure

AMOTL2 · rs13322269

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Standard

Diastolic blood pressure

FAM91A1 · rs13270541

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Standard

Diastolic blood pressure (MTAG)

AQP2 · rs12372344

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Standard

Diastolic blood pressure

NDUFAF6 · rs11781001

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Standard

Systolic blood pressure

LINC02513 · rs11721984

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Standard

Systolic blood pressure

UBN1 · rs10500326

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Standard

Diastolic blood pressure

near HMGN1P17 · rs10040811

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Standard

Diastolic blood pressure (MTAG)

GLYR1 · rs73517027

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Showing 20 of 2179 · page 47 of 109

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.