Variants in gene NEXN with conflicting interpretations "uncertain significance" and "pathogenic"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 9

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HGVS	dbSNP	gnomAD frequency
NM_144573.4(NEXN):c.835C>T (p.Arg279Cys)	rs146245480	0.00025
NM_144573.4(NEXN):c.1955A>G (p.Tyr652Cys)	rs137853197	0.00011
NM_144573.4(NEXN):c.1174C>T (p.Arg392Ter)	rs750076188	0.00004
NM_144573.4(NEXN):c.1171C>T (p.Arg391Ter)	rs200106758	0.00001
NM_144573.4(NEXN):c.1450C>T (p.Arg484Ter)	rs767792289
NM_144573.4(NEXN):c.1946GAG[1] (p.Gly650del)	rs397517853
NM_144573.4(NEXN):c.461_464del (p.Asn154fs)	rs794729088
NM_144573.4(NEXN):c.784C>T (p.Arg262Ter)	rs1002648603
NM_144573.4(NEXN):c.962del (p.Arg321fs)	rs915318065

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