List of variants in gene MC1R reported as likely benign for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 19

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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.586T>C (p.Phe196Leu)	rs3212366	0.00938
NM_002386.4(MC1R):c.252C>A (p.Asp84Glu)	rs1805006	0.00553
NM_002386.4(MC1R):c.425G>A (p.Arg142His)	rs11547464	0.00480
NM_002386.4(MC1R):c.466G>C (p.Val156Leu)	rs3212365	0.00443
NC_000016.10:g.89918089C>G	rs3212356	0.00282
NM_002386.4(MC1R):c.948C>T (p.Ser316=)	rs151318945	0.00223
NM_002386.4(MC1R):c.792C>T (p.Ile264=)	rs181269865	0.00205
NM_002386.4(MC1R):c.819C>T (p.Cys273=)	rs375813196	0.00148
NM_002386.4(MC1R):c.67C>T (p.Gln23Ter)	rs201533137	0.00144
NM_002386.4(MC1R):c.247T>C (p.Ser83Pro)	rs34474212	0.00069
NM_002386.4(MC1R):c.284C>T (p.Thr95Met)	rs34158934	0.00056
NM_002386.4(MC1R):c.200G>A (p.Arg67Gln)	rs34090186	0.00024
NM_002386.4(MC1R):c.546C>T (p.Tyr182=)	rs370040645	0.00019
NM_002386.4(MC1R):c.895G>A (p.Ala299Thr)	rs370472871	0.00016
NM_002386.4(MC1R):c.717C>T (p.Gly239=)	rs34490506	0.00012
NM_002386.4(MC1R):c.249G>A (p.Ser83=)	rs375562624	0.00004

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