ClinVar Miner

List of variants in gene NEXN reported as benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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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.*414A>C	rs1359518	0.00237

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