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

Submission 1 (likely benign) minimum review status:		Submission 1 (likely 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: 16

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HGVS	dbSNP	gnomAD frequency
NM_144573.4(NEXN):c.995A>C (p.Glu332Ala)	rs201763096	0.00262
NM_144573.4(NEXN):c.1788T>G (p.Ser596Arg)	rs199738750	0.00029
NM_144573.4(NEXN):c.242A>T (p.Asp81Val)	rs367871780	0.00028
NM_144573.4(NEXN):c.893C>G (p.Thr298Arg)	rs200753280	0.00016
NM_144573.4(NEXN):c.1435C>T (p.Leu479Phe)	rs181520023	0.00009
NM_144573.4(NEXN):c.856C>T (p.Arg286Trp)	rs199917913	0.00009
NM_144573.4(NEXN):c.865-5G>A	rs727505353	0.00005
NM_144573.4(NEXN):c.249G>A (p.Glu83=)	rs372532824	0.00004
NM_144573.4(NEXN):c.634T>A (p.Tyr212Asn)	rs769549962	0.00003
NM_144573.4(NEXN):c.1653A>G (p.Leu551=)	rs794727078	0.00001
NM_144573.4(NEXN):c.*4CT[1]	rs553696163
NM_144573.4(NEXN):c.1416AAG[1] (p.Arg475del)	rs794729091
NM_144573.4(NEXN):c.1573GAA[3] (p.Glu528del)	rs764505909
NM_144573.4(NEXN):c.1671GGA[2] (p.Glu561_Glu562del)	rs397517848
NM_144573.4(NEXN):c.1671GGA[3] (p.Glu562del)	rs397517848
NM_144573.4(NEXN):c.989AAG[2] (p.Glu332del)	rs727505124

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