ClinVar Miner

List of variants in gene FHL2 reported as likely benign for Primary dilated cardiomyopathy

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Total variants: 8
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HGVS dbSNP gnomAD frequency
NM_001318895.3(FHL2):c.85G>A (p.Val29Met) rs56284940 0.00093
NM_001318895.3(FHL2):c.84C>T (p.Cys28=) rs375234968 0.00004
NM_001318895.3(FHL2):c.156+11C>T rs371829274 0.00003
NM_001318895.3(FHL2):c.33C>T (p.Asn11=) rs760104483 0.00003
NM_001318895.3(FHL2):c.141C>T (p.Ile47=) rs757222173 0.00001
NM_001318895.3(FHL2):c.156+8C>T rs1233115186 0.00001
NM_001318895.3(FHL2):c.156+9T>C rs1573341781
NM_001318895.3(FHL2):c.72G>A (p.Glu24=)

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