List of variants in gene MYPN reported as benign by Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_032578.4(MYPN):c.1647T>C (p.Ser549=)	rs2673794	0.57747
NM_032578.4(MYPN):c.3403C>A (p.Pro1135Thr)	rs7079481	0.40619
NM_032578.4(MYPN):c.1884C>G (p.Phe628Leu)	rs10823148	0.39447
NM_032578.4(MYPN):c.2072G>A (p.Ser691Asn)	rs10997975	0.39270
NM_032578.4(MYPN):c.2120G>A (p.Ser707Asn)	rs7916821	0.39079
NM_032578.4(MYPN):c.1875C>T (p.Pro625=)	rs2673793	0.17340
NM_032578.4(MYPN):c.1178T>C (p.Val393Ala)	rs11596653	0.11086
NM_032578.4(MYPN):c.2163C>A (p.Ala721=)	rs71584491	0.04239
NM_032578.4(MYPN):c.2410G>A (p.Gly804Arg)	rs62620248	0.01839
NM_032578.4(MYPN):c.2409C>G (p.Ser803Arg)	rs3814182

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