Variants linked to Blood Pressure

Continuously updated · newest added Oct 23, 2026

2,120 positions on this site are linked to Blood Pressure, out of 108,956 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 (MTAG)

near MTND1P22 · rs13140296

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Systolic blood pressure

CLPB · rs12421674

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Diastolic blood pressure

CACNA1D · rs11915489

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Systolic blood pressure (MTAG)

LINC02235 · rs10958048

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Diastolic blood pressure

PDE10A · rs7744902

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High blood pressure / hypertension

RYK · rs7633386

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Diastolic blood pressure (MTAG)

CDC42BPA · rs7418070

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

ZSCAN16-AS1 · rs72848791

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Systolic blood pressure (MTAG)

SLC35F1 · rs62421489

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Systolic blood pressure

near HNF4G · rs2977315

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Systolic blood pressure

near INSR · rs1864009

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Systolic blood pressure (UKB data field 4080)

near SNTG1 · rs12677668

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Diastolic blood pressure (MTAG)

ARHGAP42 · rs1216744

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Diastolic blood pressure

BMS1P4-AGAP5 · rs28553894

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Systolic blood pressure (MTAG)

near CYP2C56P · rs13032768

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

STEAP2 · rs6465244

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Systolic blood pressure

TNKS · rs62491354

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Systolic blood pressure (UKB data field 4080)

FGD5 · rs1687318

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Systolic blood pressure

HSF2BP · rs162366

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Diastolic blood pressure

near KCNK5 · rs1155349

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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.