Variants linked to Blood Pressure

Continuously updated · newest added Oct 23, 2026

2,120 positions on this site are linked to Blood Pressure, out of 108,956 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

near RPL31P57 · rs28670385

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Standard

Systolic blood pressure

near C10orf55 · rs2633318

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Diastolic blood pressure

HLA-A · rs1655900

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Diastolic blood pressure

near CPMER · rs134086

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

near PCDH18 · rs10035032

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Standard

Diastolic blood pressure

PKHD1 · rs9463706

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

near HLA-DQB1 · rs9275036

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Standard

Systolic blood pressure (MTAG)

SBF1P2 · rs72864766

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Systolic blood pressure (MTAG)

JPH2 · rs7270523

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Standard

Systolic blood pressure (UKB data field 4080)

FBN2 · rs6595827

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Standard

Systolic blood pressure (MTAG)

near OR4C2P · rs616772

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Systolic blood pressure

near SKAP1 · rs56371910

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Systolic blood pressure

RP11-89M16.1 · rs4598218

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Standard

Systolic blood pressure (MTAG)

LINC02513 · rs4488948

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Diastolic blood pressure (MTAG)

MAD1L1 · rs3996330

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Systolic blood pressure

CAND1.11 · rs2084600

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Diastolic blood pressure

ATXN2 · rs17805591

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Systolic blood pressure

FURIN · rs1573644

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Systolic blood pressure

RGL3 · rs139037971

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

MAPKAP1 · rs13296765

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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.