List of variants in gene combination C2orf49, FHL2 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001318895.3(FHL2):c.321C>T (p.Thr107=)	rs139644436	0.00380
NM_001318895.3(FHL2):c.337C>T (p.Arg113Cys)	rs140148322	0.00032
NM_001318895.3(FHL2):c.174C>T (p.Asp58=)	rs141208906	0.00020

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