List of variants in gene NEXN reported by Department of Pathology and Laboratory Medicine, Sinai Health System

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_144573.4(NEXN):c.893C>G (p.Thr298Arg)	rs200753280	0.00016
NM_144573.4(NEXN):c.1053+1G>A	rs397517843	0.00007
NM_144573.4(NEXN):c.1088C>G (p.Thr363Arg)	rs748351352	0.00005
NM_144573.4(NEXN):c.1174C>T (p.Arg392Ter)	rs750076188	0.00004
NM_144573.4(NEXN):c.1946GAG[1] (p.Gly650del)	rs397517853

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