List of variants in gene NECTIN4 reported as uncertain significance for hereditary epidermal appendage anomaly

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_030916.3(NECTIN4):c.1387C>G (p.Pro463Ala)	rs142579218	0.00048
NM_030916.3(NECTIN4):c.1478G>C (p.Arg493Pro)	rs753298397
NM_030916.3(NECTIN4):c.1490C>T (p.Thr497Met)
NM_030916.3(NECTIN4):c.374A>C (p.Tyr125Ser)

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