List of variants in gene combination LOC126861898, MYH7 reported as pathogenic for Dilated cardiomyopathy 1S

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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.2389G>A (p.Ala797Thr)	rs3218716	0.00003
NM_000257.4(MYH7):c.2420G>A (p.Arg807His)	rs141414377	0.00002
NM_000257.4(MYH7):c.2292C>G (p.Phe764Leu)	rs121913643
NM_000257.4(MYH7):c.2513C>T (p.Pro838Leu)	rs397516153
NM_000257.4(MYH7):c.2539_2541del (p.Lys847del)	rs397516155

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