List of variants in gene MC1R reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_002386.4(MC1R):c.478C>T (p.Arg160Trp)	rs1805008	0.04851
NM_002386.4(MC1R):c.451C>T (p.Arg151Cys)	rs1805007	0.04832
NM_002386.4(MC1R):c.880G>C (p.Asp294His)	rs1805009	0.01121
NM_002386.4(MC1R):c.252C>A (p.Asp84Glu)	rs1805006	0.00553
NM_002386.4(MC1R):c.247T>C (p.Ser83Pro)	rs34474212	0.00069
NM_002386.4(MC1R):c.86dup (p.Asn29fs)	rs796296176

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