Variants linked to Blood Pressure

Continuously updated · newest added Oct 22, 2026

2,111 positions on this site are linked to Blood Pressure, out of 108,452 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)

SOX6 · rs17470652

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

near FOXP1 · rs13092463

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Diastolic blood pressure

TRAK1 · rs11718948

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Diastolic blood pressure

HECTD4 · rs114948768

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Systolic blood pressure (MTAG)

FGD5 · rs9814184

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

TCF7L1 · rs883650

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Diastolic blood pressure (MTAG)

DCTN2 · rs75567496

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Systolic blood pressure

near LINC02295 · rs710285

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

near SEM1 · rs6964827

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Diastolic blood pressure

near ASS1P13 · rs66682451

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

EHD4 · rs4924586

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Systolic blood pressure (MTAG)

PHACTR4 · rs4908348

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Systolic blood pressure

MTHFR · rs41394446

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Diastolic blood pressure

near RPRML · rs3851795

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Systolic blood pressure

CSTPP1 · rs138290455

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

LAMC1 · rs12404067

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Systolic blood pressure

MTHFR · rs12121543

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Systolic blood pressure

ZNF831 · rs11908189

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Systolic blood pressure

near CCN3 · rs11786573

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Diastolic blood pressure

LINC00529 · rs11780444

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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.