Variants linked to Blood Pressure

Continuously updated · newest added Oct 23, 2026

2,127 positions on this site are linked to Blood Pressure, out of 109,292 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 (MTAG)

FGGY-DT · rs12758643

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Systolic blood pressure

TSHZ3-AS1 · rs12162231

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Diastolic blood pressure

RCCD1-AS1 · rs117564299

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

LHFPL2 · rs10075895

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Standard

Diastolic blood pressure

near CSF2 · rs7721882

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Systolic blood pressure

LINC01214 · rs7636643

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Diastolic blood pressure

CACNB2 · rs7090956

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

SBF2 · rs61892596

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

SLC24A3 · rs6046140

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Systolic blood pressure

NFE2L1-DT · rs3764400

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Standard

Systolic blood pressure

LHFPL2 · rs34797797

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Standard

Systolic blood pressure (MTAG)

ATP2B1-AS1 · rs17836902

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Standard

Systolic blood pressure

near TRIM36 · rs147202915

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Standard

Diastolic blood pressure

HVCN1 · rs118156615

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Diastolic blood pressure

near LINC02120 · rs116044797

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Standard

Systolic blood pressure (MTAG)

CACNA1D · rs7340705

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

LINC02664 · rs12244754

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Diastolic blood pressure (MTAG)

ZNF652-AS1 · rs76026873

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Standard

Diastolic blood pressure

TFCP2 · rs61932870

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Standard

Systolic blood pressure (MTAG)

PLEKHG1 · rs112576472

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Showing 20 of 2127 · page 31 of 107

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.