Variants linked to Medication Use as a Genetic Trait

Continuously updated · newest added Sep 29, 2026

237 positions on this site are linked to Medication Use as a Genetic Trait, out of 19,389 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 Medication Use as a Genetic Trait

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Medication use (antihistamines for systemic use)

RBMS3 · rs1968514

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Medication use (antihistamines for systemic use)

SLC25A46 · rs10055042

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Medication use (antihistamines for systemic use)

C11orf30 · rs11236797

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Medication use (antidepressants)

SLC15A5 · rs10846305

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Medication use (anilides)

BOK-AS1 · rs7567892

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Medication use (drugs affecting bone structure and mineralization)

BTNL2 · rs9268500

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Medication use (drugs affecting bone structure and mineralization)

GNG12-AS1 · rs17130567

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Medication use (salicylic acid and derivatives)

LDLR · rs73015016

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Medication use (drugs affecting bone structure and mineralization)

MEPE · rs899040

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Medication use (salicylic acid and derivatives)

CDKN2B-AS1 · rs1831733

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Medication use (drugs affecting bone structure and mineralization)

RP11-396O20.2 · rs10832519

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Medication use (calcium channel blockers)

ENPEP · rs7685862

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Medication use (calcium channel blockers)

KDM2B · rs60370741

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Medication use (calcium channel blockers)

PRDM6 · rs1422278

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Medication use (calcium channel blockers)

ZFP91 · rs10896795

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Medication use (calcium channel blockers)

CMIP · rs7203816

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Medication use (calcium channel blockers)

FBN2 · rs6595839

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Medication use (calcium channel blockers)

PLCB1 · rs4813867

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Medication use (calcium channel blockers)

MIR4513 · rs2168518

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Medication use (calcium channel blockers)

TAGLN · rs494356

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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.