ClinVar Miner

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

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Total variants: 7
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HGVS dbSNP
NM_144573.3(NEXN):c.*22C>G rs3767028
NM_144573.3(NEXN):c.*417_*418insC rs201203673
NM_144573.3(NEXN):c.*418dupA rs368295679
NM_144573.3(NEXN):c.*511dupA rs5775432
NM_144573.3(NEXN):c.*716_*722delTGTTGAG rs145017889
NM_144573.3(NEXN):c.363G>A (p.Thr121=) rs35117963
NM_144573.3(NEXN):c.733G>A (p.Gly245Arg) rs1166698

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