ClinVar for MedGen (Select 382515) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 14311	NM_002386.4(MC1R):c.178G>T (p.Val60Leu)	MC1R (V60L)	Single nucleotide variant (missense variant)	not provided +5 more	GBenign/Likely benign
Select item 14308	NM_002386.4(MC1R):c.274G>A (p.Val92Met)	MC1R (V92M)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign