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

Diastolic blood pressure

LINC01495 · rs11026590

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Systolic blood pressure

FGGY-DT · rs9660067

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Diastolic blood pressure (MTAG)

near LINC02871 · rs6033023

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Systolic blood pressure (MTAG)

HOXD3 · rs34727427

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Diastolic blood pressure

TANC2 · rs16946721

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Systolic blood pressure

near RNA5SP188 · rs11948635

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Systolic blood pressure

near LINC01376 · rs11898255

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Diastolic blood pressure

SSPN-AS1 · rs11837982

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

XKR6 · rs10088408

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Diastolic blood pressure (UKB data field 4079)

near IRAK1BP1 · rs9341741

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

near COX14 · rs7972842

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

SUGCT · rs73322422

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Diastolic blood pressure

MAPK4 · rs58693787

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

MIR29B2CHG · rs3849274

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Standard

Diastolic blood pressure

SEMA3C · rs3807095

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Diastolic blood pressure (MTAG)

GBX1 · rs34765595

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Diastolic blood pressure

near RPL31P57 · rs28670385

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Systolic blood pressure

near C10orf55 · rs2633318

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Diastolic blood pressure

HLA-A · rs1655900

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Diastolic blood pressure

near CPMER · rs134086

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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.