C4759928[trait identifier] AND "3billion"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1705372	NM_005912.3(MC4R):c.835T>C (p.Cys279Arg)	MC4R (C279R)	Single nucleotide variant (missense variant)	BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 20	GUncertain significance
Select item 372803	NM_005912.3(MC4R):c.811T>C (p.Cys271Arg)	MC4R (C271R)	Single nucleotide variant (missense variant)	BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 20 +1 more	GPathogenic/Likely pathogenic