List of variants in gene MC1R reported by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_002386.4(MC1R):c.488G>A (p.Arg163Gln)	rs885479	0.08396
NM_002386.4(MC1R):c.178G>T (p.Val60Leu)	rs1805005	0.08197
NM_002386.4(MC1R):c.586T>C (p.Phe196Leu)	rs3212366	0.00938
NM_002386.4(MC1R):c.466G>C (p.Val156Leu)	rs3212365	0.00443
NM_002386.4(MC1R):c.112G>A (p.Val38Met)	rs200050206	0.00040
NM_002386.4(MC1R):c.200G>A (p.Arg67Gln)	rs34090186	0.00024
NM_002386.4(MC1R):c.332C>T (p.Ala111Val)	rs201489928	0.00021
NM_002386.4(MC1R):c.577G>A (p.Val193Met)	rs527673999	0.00011
NM_002386.4(MC1R):c.803C>G (p.Pro268Arg)	rs527697723	0.00010
NM_002386.4(MC1R):c.766C>T (p.Pro256Ser)	rs200215218	0.00008
NM_002386.4(MC1R):c.104G>A (p.Cys35Tyr)	rs779504604	0.00003
NM_002386.4(MC1R):c.583T>G (p.Phe195Val)	rs377580634	0.00002
NM_002386.4(MC1R):c.313G>A (p.Ala105Thr)	rs1376244060	0.00001
NM_002386.4(MC1R):c.265G>C (p.Gly89Arg)	rs34540312
NM_002386.4(MC1R):c.795C>G (p.Val265=)	rs367998996

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