List of variants in gene MC4R reported as uncertain significance 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
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_005912.3(MC4R):c.719A>G (p.Asn240Ser)	rs202228712	0.00043
NM_005912.3(MC4R):c.523G>A (p.Ala175Thr)	rs121913563	0.00031
NM_005912.3(MC4R):c.-121G>A	rs541962206	0.00003
NM_005912.3(MC4R):c.31A>G (p.Thr11Ala)	rs372794914	0.00003
NM_005912.3(MC4R):c.691G>A (p.Gly231Ser)	rs1363347811	0.00003
NM_005912.3(MC4R):c.14C>A (p.Thr5Asn)	rs752432398	0.00001
NM_005912.3(MC4R):c.239A>G (p.Tyr80Cys)	rs1368643838	0.00001
NM_005912.3(MC4R):c.827A>G (p.Tyr276Cys)	rs748627503	0.00001
NM_005912.3(MC4R):c.883T>C (p.Ser295Pro)	rs368264587	0.00001
NM_005912.3(MC4R):c.-59G>A	rs750662653
NM_005912.3(MC4R):c.53G>T (p.Arg18Leu)	rs780671601
NM_005912.3(MC4R):c.815C>G (p.Pro272Arg)	rs1915338291
NM_005912.3(MC4R):c.914G>A (p.Arg305Gln)	rs775382722

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