List of variants in gene combination C2orf49, FHL2 reported as benign for Primary dilated 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001318895.3(FHL2):c.688+12G>T	rs2278502	0.31336
NM_001318895.3(FHL2):c.689-12C>G	rs2244182	0.21176
NM_001318895.3(FHL2):c.819C>T (p.Pro273=)	rs11124029	0.16120
NM_001318895.3(FHL2):c.804C>T (p.Asp268=)	rs3087523	0.08785
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.331+16T>C	rs76372678	0.00659
NM_001318895.3(FHL2):c.689-10C>G	rs115841332	0.00456
NM_001318895.3(FHL2):c.321C>T (p.Thr107=)	rs139644436	0.00380
NM_001318895.3(FHL2):c.207G>A (p.Ser69=)	rs138189036	0.00036
NM_001318895.3(FHL2):c.402G>C (p.Gln134His)	rs199585402	0.00018
NM_001318895.3(FHL2):c.332-7A>G	rs748658755	0.00014
NM_001318895.3(FHL2):c.192C>T (p.Ala64=)	rs199943518	0.00011
NM_001318895.3(FHL2):c.336C>G (p.Thr112=)

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