Variants linked to Blood Pressure

Continuously updated · newest added Oct 23, 2026

2,151 positions on this site are linked to Blood Pressure, out of 109,880 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

LIMA1 · rs7967954

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Systolic blood pressure (MTAG)

near LINC02227 · rs2419923

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Diastolic blood pressure

CACNB2 · rs7911644

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Systolic blood pressure

near RPS4XP9 · rs13220350

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

SDCCAG8 · rs10926989

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Diastolic blood pressure

SLC17A1 · rs62394271

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Systolic blood pressure

MECOM · rs56743174

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Standard

Systolic blood pressure (MTAG)

ATP2B1-AS1 · rs4842679

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Diastolic blood pressure

SDCCAG8 · rs10926978

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

near CCN3 · rs17792171

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Diastolic blood pressure (MTAG)

LINC00533 · rs11966966

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Systolic blood pressure (MTAG)

CERS5 · rs35998534

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Systolic blood pressure

BAG6 · rs2077492

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

near RXFP2 · rs1006095

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Diastolic blood pressure (MTAG)

ATP2B1-AS1 · rs11105383

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Diastolic blood pressure

ULK4 · rs2683696

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Diastolic blood pressure (MTAG)

CUX2 · rs7963641

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

near BORCS7-ASMT · rs185575325

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Diastolic blood pressure (BMI adjusted)

AS3MT · rs11191454

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Systolic blood pressure (MTAG)

ZNF831 · rs11906755

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Showing 20 of 2151 · page 40 of 108

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.