Variants linked to Alcohol Consumption

Continuously updated · newest added Sep 25, 2026

85 positions on this site are linked to Alcohol Consumption, out of 16,306 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 Alcohol Consumption

Standard

Pulse pressure x alcohol consumption interaction (2df test)

UNC5D · rs79505281

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Standard

Pulse pressure x alcohol consumption interaction (2df test)

LOC105372361 · rs142673685

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Standard

Pulse pressure x alcohol consumption interaction (2df test)

ELMOD1 · rs139077481

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Standard

Pulse pressure x alcohol consumption interaction (2df test)

LOC105377655 · rs17083718

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Standard

Pulse pressure x alcohol consumption interaction (2df test)

LOC105372045 · rs140520944

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Standard

Mean arterial pressure x alcohol consumption (light vs heavy) interaction (2df test)

FES · rs1894400

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Standard

Mean arterial pressure x alcohol consumption (light vs heavy) interaction (2df test)

GUCY1A3 · rs11725969

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Standard

Alcohol consumption

CADM2 · rs9841829

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Standard

Alcohol consumption

CTNNA2 · rs140089781

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Alcohol consumption in current drinkers

ARID4A · rs8012947

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Alcohol consumption in current drinkers

CADM2 · rs13078384

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Alcohol consumption

near EIF4E · rs144198753

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Standard

Alcohol consumption

CADM2 · rs1376935

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Alcohol consumption

TSPAN5 · rs114026228

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Alcohol consumption

ADH1B · rs145452708

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Alcohol consumption

ADH5 · rs29001570

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Alcohol consumption

KLB · rs28712821

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Alcohol consumption

BDNF · rs988748

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Alcohol consumption

KLB · rs11940694

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Standard

Longitudinal alcohol consumption

LOC100129340 · rs7031417

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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.