List of variants in gene NEXN 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_144573.4(NEXN):c.586C>T (p.Arg196Cys)	rs369486891	0.00007
NM_144573.4(NEXN):c.1453G>A (p.Glu485Lys)	rs368812830	0.00006
NM_144573.4(NEXN):c.865-5G>A	rs727505353	0.00005
NM_144573.4(NEXN):c.1619T>C (p.Met540Thr)	rs531641059	0.00001
NM_144573.4(NEXN):c.1175G>A (p.Arg392Gln)	rs971313210
NM_144573.4(NEXN):c.1238A>G (p.Gln413Arg)	rs1650473441
NM_144573.4(NEXN):c.1573GAA[3] (p.Glu528del)	rs764505909
NM_144573.4(NEXN):c.1630del (p.Gln544fs)	rs730880172

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