Variants linked to Osteoporosis

Continuously updated · newest added Oct 24, 2026

17 positions on this site are linked to Osteoporosis, out of 113,825 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 Osteoporosis

Standard

Osteoporosis

near GALNT3 · rs10204976

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Osteoporosis

LRP5 · rs880610

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Osteoporosis (additive model)

LRP5 · rs56154705

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Osteoporosis

near HLA-DRB9 · rs2071805

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Osteoporosis, osteopenia and pathological fracture (PheCode 743)

near MRPS31P1 · rs4437116

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Osteoporosis (PheCode 743.1)

SEM1 · rs6960700

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Osteoporosis, osteopenia and pathological fracture (PheCode 743)

near HLA-DRB1 · rs114335056

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Standard

Osteoporosis, osteopenia and pathological fracture (PheCode 743)

near PPIAP34 · rs34568051

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Osteoporosis NOS (PheCode 743.11)

near MRPS31P1 · rs87939

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Osteoporosis, osteopenia and pathological fracture (PheCode 743)

LINC01700 · rs2836800

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Osteoporosis, osteopenia and pathological fracture (PheCode 743)

near SUPT3H · rs227831

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Osteoporosis NOS (PheCode 743.11)

FAM3C · rs56364616

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Fracture

RPS6KA5 · rs1286083

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Fracture

CTNNB1 · rs430727

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Fracture

MBL2 · rs11003047

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Osteoporosis-related phenotypes

RAP1A · rs494453

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Osteoporosis

ALDH7A1 · rs13182402

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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.