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

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_144573.4(NEXN):c.995A>C (p.Glu332Ala)	rs201763096	0.00291
NM_144573.4(NEXN):c.249G>A (p.Glu83=)	rs372532824	0.00003
NM_144573.4(NEXN):c.*4CT[1]	rs553696163
NM_144573.4(NEXN):c.1573GAA[3] (p.Glu528del)	rs764505909

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