List of variants in gene MC4R reported as uncertain significance by Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_005912.3(MC4R):c.307G>A (p.Val103Ile)	rs2229616	0.01533
NM_005912.3(MC4R):c.751A>C (p.Ile251Leu)	rs52820871	0.00774
NM_005912.2(MC4R):c.110A>T (p.Asp37Val)	rs13447325	0.00013
NM_005912.3(MC4R):c.914G>A (p.Arg305Gln)	rs775382722

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