List of variants in gene combination MHRT, MYH7 reported by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000257.4(MYH7):c.4377G>T (p.Lys1459Asn)	rs201307101	0.00024
NM_000257.4(MYH7):c.4389G>A (p.Ser1463=)	rs781203524	0.00002
NM_000257.4(MYH7):c.4424G>A (p.Arg1475His)	rs1176998293	0.00001
NM_000257.4(MYH7):c.4512C>T (p.Asn1504=)	rs1219572407	0.00001
NM_000257.4(MYH7):c.4276G>A (p.Glu1426Lys)	rs397516208
NM_000257.4(MYH7):c.4399C>G (p.Leu1467Val)	rs397516214
NM_000257.4(MYH7):c.4402G>A (p.Glu1468Lys)	rs876657884
NM_000257.4(MYH7):c.4463A>G (p.Tyr1488Cys)	rs948329167
NM_000257.4(MYH7):c.4616A>G (p.Glu1539Gly)	rs1446214564

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