Variants linked to Blood Pressure

Continuously updated · newest added Oct 23, 2026

2,125 positions on this site are linked to Blood Pressure, out of 109,124 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 (DBP, mean, inv-normal transformed)

STEAP2 · rs6465244

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Systolic blood pressure

TNKS · rs62491354

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Systolic blood pressure (UKB data field 4080)

FGD5 · rs1687318

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Systolic blood pressure

HSF2BP · rs162366

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Diastolic blood pressure

near KCNK5 · rs1155349

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

CEP83 · rs74340001

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

near CCN3 · rs73713589

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Diastolic blood pressure

CHD6 · rs7265695

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Diastolic blood pressure

HM13-AS1 · rs6060114

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Diastolic blood pressure

NGF-AS1 · rs113806982

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Diastolic blood pressure (MTAG)

NPR3 · rs10053638

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Diastolic blood pressure (UKB data field 4079)

near HERPUD2 · rs343039

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Diastolic blood pressure (MTAG)

near GLS · rs1860172

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Essential hypertension (PheCode 401.1)

SLC27A6 · rs1363470

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Systolic blood pressure

ARHGAP42 · rs6590820

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Systolic blood pressure

ATXN1 · rs179991

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Diastolic blood pressure

near MUC22 · rs1632855

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Systolic blood pressure

ZBTB38 · rs73872710

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Diastolic blood pressure

MAPKBP1 · rs4923910

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Diastolic blood pressure (MTAG)

ULK4 · rs144282473

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Showing 20 of 2125 · page 29 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.