Variants linked to Blood Pressure

Continuously updated · newest added Oct 23, 2026

2,132 positions on this site are linked to Blood Pressure, out of 109,418 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

FBN2 · rs1435514

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Systolic blood pressure (MTAG)

ATP2B1 · rs12581002

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Diastolic blood pressure (MTAG)

HVCN1 · rs117252984

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Systolic blood pressure

near OR4C12 · rs10769647

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Systolic blood pressure

NRXN1 · rs10190857

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Diastolic blood pressure (UKB data field 4079)

near SCGN · rs9467545

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Diastolic blood pressure (MTAG)

near ABT1 · rs75018140

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Systolic blood pressure (MTAG)

near MIR548AZ · rs2470004

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Diastolic blood pressure

LINC02580 · rs2374457

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Diastolic blood pressure (MTAG)

near KRT18P16 · rs10052105

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Systolic blood pressure (MTAG)

near RNU1-96P · rs2055120

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Systolic blood pressure

near GNPATP · rs8053059

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Diastolic blood pressure

SDCCAG8 · rs10926991

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

ABHD17C · rs8031196

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Diastolic blood pressure

near LINC01819 · rs76099932

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Systolic blood pressure (MTAG)

CADM2 · rs1375564

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Systolic blood pressure

ZNF652-AS1 · rs12944684

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

PDE1A · rs12475647

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Systolic blood pressure

near KIAA2013 · rs71647020

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Diastolic blood pressure

CHD6 · rs6065365

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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.