List of variants in gene LOC126805765, NEXN studied for Cardiomyopathy

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_144573.4(NEXN):c.363G>A (p.Thr121=)	rs35117963	0.01181
NM_144573.4(NEXN):c.299-3T>C	rs397517856	0.00001
NM_144573.4(NEXN):c.341_342del (p.Gln114fs)	rs397517857	0.00001
NM_144573.4(NEXN):c.373C>T (p.Arg125Ter)	rs773500471	0.00001
NM_144573.4(NEXN):c.380G>A (p.Arg127His)	rs776891268	0.00001
NM_144573.4(NEXN):c.421C>T (p.Arg141Cys)	rs536537549	0.00001
NM_144573.4(NEXN):c.337A>G (p.Arg113Gly)	rs1302079359
NM_144573.4(NEXN):c.408G>A (p.Lys136=)	rs2102094793

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