Variants linked to Blood Pressure

Continuously updated · newest added Oct 22, 2026

2,098 positions on this site are linked to Blood Pressure, out of 107,852 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

ENPEP · rs2881854

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Diastolic blood pressure

near BCAS3 · rs2286525

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Diastolic blood pressure

near HOXA13 · rs10228276

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Diastolic blood pressure

near GUCY1A1 · rs7436887

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Diastolic blood pressure

JPH2 · rs6031431

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Diastolic blood pressure

LSP1 · rs569550

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Diastolic blood pressure

near LRRC10B · rs751985

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Diastolic blood pressure

CYP11B1–CYP11B2 · rs62525059

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Diastolic blood pressure

FGD5 · rs78793397

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Systolic blood pressure

CACNA1D · rs9814480

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Systolic blood pressure

LSP1 · rs4980389

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Systolic blood pressure

RPTOR · rs139293840

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Diastolic blood pressure

ATP2B1 · rs111478946

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Diastolic blood pressure

CACNA1D · rs3774447

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Diastolic blood pressure

KCNK3 · rs1275982

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Diastolic blood pressure

LOC102723639 · rs35443

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Diastolic blood pressure

EML6 · rs72806698

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Diastolic blood pressure

YES1 · rs8084192

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Diastolic blood pressure

CACNA1D · rs3774427

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Systolic blood pressure

WNT2B · rs10776752

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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.