Variants linked to Blood Pressure

Continuously updated · newest added Oct 23, 2026

2,205 positions on this site are linked to Blood Pressure, out of 112,649 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

WNT2B · rs72699046

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

COL21A1 · rs12216230

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Systolic blood pressure (MTAG)

near LINC01219 · rs217230

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Diastolic blood pressure

near PDE3A-AS1 · rs10841486

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Diastolic blood pressure

near PRPS1P1 · rs7556898

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Diastolic blood pressure

PDE10A · rs59641479

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Diastolic blood pressure (MTAG)

NHERF2 · rs28698483

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Systolic blood pressure

NPR3 · rs1847018

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

MARK2P10 · rs12533044

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Diastolic blood pressure

HDAC7 · rs11168245

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

GUCY1A1 · rs6839022

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Diastolic blood pressure

SEPTIN9 · rs77946446

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Systolic blood pressure

near MTND1P22 · rs7683728

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Diastolic blood pressure

GPR137B · rs10924415

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Diastolic blood pressure (MTAG)

LINC02227 · rs2963452

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Diastolic blood pressure

near TCP1P3 · rs4762911

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Diastolic blood pressure

NGF-AS1 · rs145339349

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

ABHD17C · rs2627308

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Diastolic blood pressure

MYEOV · rs11228620

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Systolic blood pressure

near LINC01478 · rs56407827

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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.