List of variants in gene combination EDAR, RANBP2 reported as uncertain significance for Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive; Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_022336.4(EDAR):c.319A>G (p.Met107Val)	rs61761321	0.00302
NM_022336.4(EDAR):c.1138A>C (p.Ser380Arg)	rs146567337	0.00095
NM_022336.4(EDAR):c.871G>A (p.Ala291Thr)	rs200267845	0.00013

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