Variants linked to Blood Pressure

Continuously updated · newest added Oct 22, 2026

2,108 positions on this site are linked to Blood Pressure, out of 108,284 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 (SBP, mean, inv-normal transformed)

METTL15 · rs11030306

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Systolic blood pressure

ATP2B1 · rs10858915

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

LINC02373 · rs7967509

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Systolic blood pressure (UKB data field 4080)

SBF2 · rs7942000

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Systolic blood pressure

near CDYL2 · rs79402702

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Diastolic blood pressure

UMOD · rs7203451

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Systolic blood pressure

near MIR148A · rs6965388

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Diastolic blood pressure (MTAG)

near MXD4 · rs61789369

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Systolic blood pressure

ZBTB46-AS1 · rs6062324

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Diastolic blood pressure

PREX1 · rs6019378

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Standard

Systolic blood pressure (UKB data field 4080)

SCAI · rs60042780

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Diastolic blood pressure

CREBRF · rs594140

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Diastolic blood pressure

BNC1 · rs4480763

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Systolic blood pressure (MTAG)

USP38-DT · rs4309787

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Diastolic blood pressure (MTAG)

PPM1E · rs36071323

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Diastolic blood pressure (MTAG)

near CATSPER2 · rs2927071

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Systolic blood pressure

NME7 · rs2179490

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Systolic blood pressure (MTAG)

SOX6 · rs17470652

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systolic blood pressure (SBP, maximum, inv-normal transformed)

near FOXP1 · rs13092463

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Diastolic blood pressure

TRAK1 · rs11718948

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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.