List of variants in gene combination LOC126861897, MYH7 reported as likely benign for Cardiomyopathy

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000257.4(MYH7):c.5253T>C (p.Ala1751=)	rs776282574	0.00004
NM_000257.4(MYH7):c.5280G>A (p.Thr1760=)	rs374803185	0.00003
NM_000257.4(MYH7):c.5286C>T (p.Ala1762=)	rs771432461	0.00002
NM_000257.4(MYH7):c.5229G>A (p.Glu1743=)	rs149509691
NM_000257.4(MYH7):c.5265C>A (p.Ala1755=)	rs2138639281

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