List of variants in gene combination LOC126861898, MYH7 reported as uncertain significance for Myosin storage myopathy

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000257.4(MYH7):c.2334C>T (p.Asp778=)	rs2069544	0.00035
NM_000257.4(MYH7):c.2526T>C (p.Ser842=)	rs554560162	0.00013
NM_000257.4(MYH7):c.2335G>A (p.Glu779Lys)	rs1427104281
NM_000257.4(MYH7):c.2424-7C>T	rs759141144

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