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

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) 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: 17

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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.1659+18C>G	rs147422621	0.00228
NM_144573.4(NEXN):c.864+12T>A	rs188416492	0.00141
NM_144573.4(NEXN):c.156C>T (p.Asp52=)	rs371431782	0.00128
NM_144573.4(NEXN):c.1618A>G (p.Met540Val)	rs201390657	0.00113
NM_144573.4(NEXN):c.777A>G (p.Gln259=)	rs375544798	0.00077
NM_144573.4(NEXN):c.732C>A (p.Pro244=)	rs201171783	0.00045
NM_144573.4(NEXN):c.1785C>T (p.Asp595=)	rs182998780	0.00041
NM_144573.4(NEXN):c.512T>C (p.Ile171Thr)	rs372065024	0.00035
NM_144573.4(NEXN):c.1029G>A (p.Ala343=)	rs374260457	0.00023
NM_144573.4(NEXN):c.865-17A>G	rs201771600	0.00016
NM_144573.4(NEXN):c.949A>C (p.Met317Leu)	rs559464457	0.00009
NM_144573.4(NEXN):c.78T>C (p.Leu26=)	rs376535223	0.00008
NM_144573.4(NEXN):c.1065T>C (p.Asp355=)	rs369897647	0.00004
NM_144573.4(NEXN):c.249G>A (p.Glu83=)	rs372532824	0.00004
NM_144573.4(NEXN):c.66T>C (p.Tyr22=)	rs749182975	0.00001
NM_144573.4(NEXN):c.1573GAA[3] (p.Glu528del)	rs764505909

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