Variants linked to Blood Pressure

Continuously updated · newest added Oct 22, 2026

2,116 positions on this site are linked to Blood Pressure, out of 108,788 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

PPP1R1C · rs10197864

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Takes medication for high blood pressure?

near PCDH18 · rs9685314

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Systolic blood pressure

LINC02052 · rs62290738

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Systolic blood pressure

SLC8A1 · rs11893746

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Diastolic blood pressure

PIEZO2 · rs10853191

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

ICA1L · rs80087860

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Diastolic blood pressure (MTAG)

near SLC39A12 · rs7917532

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Diastolic blood pressure (UKB data field 4079)

COL4A1 · rs751749

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Systolic blood pressure

RP11-444A22.1 · rs72816333

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Diastolic blood pressure (long-term average)

ULK4 · rs6599176

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

SENP7 · rs34407049

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Systolic blood pressure (MTAG)

ATP2B1-AS1 · rs149193253

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Diastolic blood pressure (UKB data field 4079)

near CACNB2 · rs12570727

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

GLCE · rs11629932

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Systolic blood pressure

AK094674 · rs11263441

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Systolic blood pressure

near XPR1 · rs10914057

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Diastolic blood pressure

near KRT18P16 · rs6893502

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Systolic blood pressure

INPP5A · rs56092448

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Diastolic blood pressure (MTAG)

PDGFC · rs1425486

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Diastolic blood pressure (MTAG)

SLC39A8 · rs11724128

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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.