Variants linked to Blood Pressure

Continuously updated · newest added Oct 23, 2026

2,198 positions on this site are linked to Blood Pressure, out of 112,485 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)

ST6GALNAC6 · rs2417060

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Standard

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

FBN1 · rs625034

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Standard

Diastolic blood pressure

near PDE3A-AS1 · rs17375682

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Standard

Systolic blood pressure

ATG7 · rs9848170

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Standard

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

TBC1D10A · rs737948

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Standard

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

RPL39L · rs77209823

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Standard

Diastolic blood pressure

ZNF831 · rs6026729

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Standard

Diastolic blood pressure

near PINX1-DT · rs6989160

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Standard

Systolic blood pressure (MTAG)

NGF-AS1 · rs59980837

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Standard

Diastolic blood pressure

NFKB1-AS1 · rs13140033

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Standard

Systolic blood pressure (MTAG)

near LINC02120 · rs1494651

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Standard

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

MIR29B2CHG · rs12132780

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Standard

Diastolic blood pressure

FBN2 · rs4836377

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Standard

Diastolic blood pressure

WNT2B · rs72699046

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Standard

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

COL21A1 · rs12216230

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Standard

Systolic blood pressure (MTAG)

near LINC01219 · rs217230

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Standard

Diastolic blood pressure

near PDE3A-AS1 · rs10841486

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Standard

Diastolic blood pressure

near PRPS1P1 · rs7556898

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Standard

Diastolic blood pressure

PDE10A · rs59641479

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Standard

Diastolic blood pressure (MTAG)

NHERF2 · rs28698483

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Showing 20 of 2198 · page 58 of 110

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.