ClinVar Miner

List of variants in gene ACTN2 reported as likely benign for Hypertrophic cardiomyopathy

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Total variants: 18
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HGVS dbSNP
NM_001103.3(ACTN2):c.*1087G>A rs11801672
NM_001103.3(ACTN2):c.*111A>G rs1051251
NM_001103.3(ACTN2):c.*423A>G rs114880747
NM_001103.3(ACTN2):c.*447C>G rs1051253
NM_001103.3(ACTN2):c.*526T>C rs1803032
NM_001103.3(ACTN2):c.*700A>G rs12733179
NM_001103.3(ACTN2):c.*724G>C rs7532533
NM_001103.3(ACTN2):c.*748A>G rs7522310
NM_001103.3(ACTN2):c.*954G>A rs2153203
NM_001103.3(ACTN2):c.-22C>T rs138279482
NM_001103.3(ACTN2):c.-98_-92CGCCGCC[2] rs552471202
NM_001103.3(ACTN2):c.1296G>A (p.Ala432=) rs35956798
NM_001103.3(ACTN2):c.1423G>A (p.Asp475Asn) rs80257412
NM_001103.3(ACTN2):c.1810A>G (p.Met604Val) rs35997569
NM_001103.3(ACTN2):c.2139G>A (p.Thr713=) rs34975493
NM_001103.3(ACTN2):c.2610G>A (p.Ser870=) rs12063382
NM_001103.3(ACTN2):c.705G>C (p.Val235=) rs2288599
NM_001103.3(ACTN2):c.877-8C>G rs2288601

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