ClinVar Miner

List of variants in gene NEXN reported as uncertain significance for Primary familial hypertrophic cardiomyopathy

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Total variants: 7
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HGVS dbSNP
NM_144573.3(NEXN):c.1400T>C (p.Ile467Thr) rs370195451
NM_144573.3(NEXN):c.1435C>T (p.Leu479Phe) rs181520023
NM_144573.3(NEXN):c.2005C>T (p.Leu669Phe) rs774194309
NM_144573.3(NEXN):c.856C>T (p.Arg286Trp) rs199917913
NM_144573.4(NEXN):c.1053+1G>A rs397517843
NM_144573.4(NEXN):c.1996A>G (p.Thr666Ala) rs374000722
NM_144573.4(NEXN):c.835C>T (p.Arg279Cys) rs146245480

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