BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 20: genes and variants

BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 20 is linked to 2 analyzed proteins (MC4R and PCSK1). 8 DNA variants are known to cause it; 22 more are uncertain, and 0 of those already look disease-causing on computable evidence.

Last updated 2026-09-30. Research information, not medical advice.

Also known as: Body mass index quantitative trait locus 12

Genes linked to BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 20

Where BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 20 variants cluster

Known disease-causing variants in BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 20

VariantPositionProtein partClinical label
MC4R R165Q165CytoplasmicDisease-causing (★★★★)
MC4R R165G165CytoplasmicDisease-causing (★★★★)
MC4R R165W165CytoplasmicDisease-causing (★★★★)
MC4R I316S316CytoplasmicDisease-causing (★★)
MC4R F51L51TransmembraneDisease-causing
MC4R N97D97TransmembraneDisease-causing
MC4R I102S102TransmembraneDisease-causing
MC4R S58C58TransmembraneDisease-causing

Which prediction tools work for BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 20

How often each tool ranks a disease-causing variant above a harmless one (AUROC × 100).

Same protein, different disease

Diseases related to BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 20

Frequently asked questions

Which genes are linked to BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 20?

In CATVariant, BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 20 is linked to 2 analyzed proteins: MC4R (Melanocortin receptor 4) and PCSK1 (Neuroendocrine convertase 1).

How many genetic variants are linked to BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 20?

32 variants: 8 are classified as disease-causing (pathogenic or likely pathogenic) in ClinVar and 22 are of uncertain significance or have conflicting reports.

Which uncertain variants in BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 20 look disease-causing?

None of the uncertain variants currently reaches the likely-pathogenic range on computable evidence alone.

About this data

Variant–disease links come from ClinVar, Open Targets and UniProt, pooled from the latest public CATVariant analysis of each human protein. Evidence scores use the ACMG/AMP Bayesian points scale with computable criteria only (position among known disease variants, rarity in gnomAD, calibrated predictors, deep mutational scanning); there is no family or patient data, so they prioritise variants for expert review and never classify them.

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