List of variants in gene FHL2 reported as uncertain significance 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: 28

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HGVS	dbSNP	gnomAD frequency
NM_001318895.3(FHL2):c.121G>A (p.Glu41Lys)	rs552625336	0.00004
NM_001318895.3(FHL2):c.104T>G (p.Leu35Arg)	rs1470032926	0.00001
NM_001318895.3(FHL2):c.130G>A (p.Gly44Arg)	rs780938900	0.00001
NM_001318895.3(FHL2):c.72G>C (p.Glu24Asp)	rs781170250	0.00001
NC_000002.11:g.(?_105977730)_(106002983_?)dup
NM_001318895.3(FHL2):c.109G>A (p.Ala37Thr)	rs74575749
NM_001318895.3(FHL2):c.10C>A (p.Arg4Ser)
NM_001318895.3(FHL2):c.11G>C (p.Arg4Pro)	rs369109946
NM_001318895.3(FHL2):c.121G>T (p.Glu41Ter)	rs552625336
NM_001318895.3(FHL2):c.125A>G (p.Glu42Gly)	rs1045395933
NM_001318895.3(FHL2):c.128G>A (p.Cys43Tyr)	rs745717988
NM_001318895.3(FHL2):c.139A>G (p.Ile47Val)	rs1682314685
NM_001318895.3(FHL2):c.142G>A (p.Gly48Ser)	rs777846521
NM_001318895.3(FHL2):c.143G>A (p.Gly48Asp)	rs1196386664
NM_001318895.3(FHL2):c.154A>G (p.Lys52Glu)
NM_001318895.3(FHL2):c.29G>A (p.Cys10Tyr)	rs1682328689
NM_001318895.3(FHL2):c.2T>C (p.Met1Thr)
NM_001318895.3(FHL2):c.4A>G (p.Thr2Ala)
NM_001318895.3(FHL2):c.56A>G (p.Tyr19Cys)
NM_001318895.3(FHL2):c.56A>T (p.Tyr19Phe)
NM_001318895.3(FHL2):c.62T>A (p.Leu21Gln)	rs755805016
NM_001318895.3(FHL2):c.64C>T (p.Arg22Trp)
NM_001318895.3(FHL2):c.65G>A (p.Arg22Gln)
NM_001318895.3(FHL2):c.73dup (p.Ser25fs)	rs1682322677
NM_001318895.3(FHL2):c.74G>A (p.Ser25Asn)
NM_001318895.3(FHL2):c.81C>A (p.Tyr27Ter)	rs727503060
NM_001318895.3(FHL2):c.82T>C (p.Cys28Arg)
NM_001318895.3(FHL2):c.86T>C (p.Val29Ala)

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