List of variants in gene NEXN reported as uncertain significance for Dilated cardiomyopathy 1CC

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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: 14

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HGVS	dbSNP	gnomAD frequency
NM_144573.4(NEXN):c.1955A>G (p.Tyr652Cys)	rs137853197	0.00011
NM_144573.4(NEXN):c.1088C>G (p.Thr363Arg)	rs748351352	0.00005
NM_144573.4(NEXN):c.1174C>T (p.Arg392Ter)	rs750076188	0.00004
NM_144573.4(NEXN):c.857G>A (p.Arg286Gln)	rs910594117	0.00003
NM_144573.4(NEXN):c.1739G>A (p.Gly580Glu)	rs560530481	0.00001
NC_000001.11:g.77926856_77926858del
NM_144573.4(NEXN):c.1401AGA[2] (p.Glu470del)	rs397517846
NM_144573.4(NEXN):c.1573GAA[3] (p.Glu528del)	rs764505909
NM_144573.4(NEXN):c.1640T>A (p.Ile547Asn)	rs753636624
NM_144573.4(NEXN):c.178C>T (p.Gln60Ter)	rs1649088164
NM_144573.4(NEXN):c.1946GAG[1] (p.Gly650del)	rs397517853
NM_144573.4(NEXN):c.633A>T (p.Arg211Ser)	rs745502254
NM_144573.4(NEXN):c.646C>T (p.Arg216Ter)	rs763730619
NM_144573.4(NEXN):c.859C>T (p.Gln287Ter)	rs1402442744

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