List of variants in gene combination MHRT, MYH7 reported as uncertain significance for Myosin storage myopathy

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_000257.4(MYH7):c.4377G>T (p.Lys1459Asn)	rs201307101	0.00024
NM_000257.4(MYH7):c.4293C>T (p.Asp1431=)	rs45560242	0.00008
NM_000257.4(MYH7):c.4519+6C>T	rs370779504	0.00005
NM_000257.4(MYH7):c.4410G>A (p.Ser1470=)	rs578166720	0.00004
NM_000257.4(MYH7):c.4557C>T (p.Ser1519=)	rs150552664	0.00002
NM_000257.4(MYH7):c.4321G>T (p.Ala1441Ser)	rs745414245	0.00001
NM_000257.4(MYH7):c.4487A>C (p.Glu1496Ala)	rs397516218	0.00001
NM_000257.4(MYH7):c.4525A>C (p.Ile1509Leu)	rs397516221	0.00001
NM_000257.4(MYH7):c.4285_4287del (p.Met1429del)	rs1892274161
NM_000257.4(MYH7):c.4395G>A (p.Ser1465=)	rs397516213

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