Variants linked to Heel Bone Mineral Density

Continuously updated · newest added Sep 16, 2026

459 positions on this site are linked to Heel Bone Mineral Density, out of 12,257 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

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Standard

Heel bone mineral density

COL1A1 · rs79409705

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Heel bone mineral density

C17orf82 · rs740753

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Heel bone mineral density

NFE2L1 · rs9909922

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Heel bone mineral density

TLK2 · rs118172483

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Heel bone mineral density

BCAS3 · rs138852655

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Heel bone mineral density

AXIN2 · rs4541111

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Heel bone mineral density

MMD · rs11079166

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Heel bone mineral density

RGS9 · rs9896306

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Heel bone mineral density

ACSF2 · rs58383597

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Heel bone mineral density

TMEM92 · rs2586457

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Heel bone mineral density

ANKFN1 · rs60891864

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Heel bone mineral density

STAT5A · rs9908318

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Heel bone mineral density

PRCAT47 · rs2549722

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Heel bone mineral density

NTN1 · rs11078776

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Heel bone mineral density

MIR193A · rs62063930

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Heel bone mineral density

SOST · rs7217502

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Heel bone mineral density

NTN1 · rs12938040

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Heel bone mineral density

SPG7 · rs57696383

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Heel bone mineral density

PIEZO1 · rs2272443

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Heel bone mineral density

LOC101928614 · rs11866031

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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.