List of variants in gene combination C2orf49, FHL2 reported as 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001318895.3(FHL2):c.530G>A (p.Arg177Gln)	rs113188481	0.01458
NM_001318895.3(FHL2):c.678C>T (p.Asn226=)	rs137869171	0.00794
NM_001318895.3(FHL2):c.689-10C>G	rs115841332	0.00456
NM_001318895.3(FHL2):c.207G>A (p.Ser69=)	rs138189036	0.00033

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