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

Diastolic blood pressure

SLC7A1 · rs9508495

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Diastolic blood pressure

PCDH9 · rs9571670

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Diastolic blood pressure

DHODH · rs9928078

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Diastolic blood pressure

ENPEP · rs9994289

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Systolic blood pressure x depressive symptoms (dichotomous) interaction (2df test)

DOCK4 · rs757194

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Diastolic blood pressure x depressive symptoms (quantitative) interaction (1df test)

near UBE2K · rs145132348

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Pulse pressure

FAF1 · rs147696085

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Pulse pressure

SARNP · rs143118162

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Pulse pressure

FBN1 · rs1678981

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Pulse pressure

SMOC2 · rs1322639

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Pulse pressure

HOMEZ · rs12050260

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Pulse pressure

LNX1-AS2 · rs11725861

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Pulse pressure

SYT4 · rs12606620

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Systolic blood pressure

near WNT9B · rs75230966

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Systolic blood pressure

PRKRIR · rs7927515

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Systolic blood pressure

RYK · rs75305034

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Systolic blood pressure

RABGAP1 · rs10818775

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Pulse pressure

H1FNT · rs1489110

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Pulse pressure

CCDC65 · rs138650910

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Pulse pressure

LRP1 · rs7968719

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Showing 20 of 2179 · page 82 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.