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

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Total variants: 5

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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	0.00054
NM_022336.4(EDAR):c.871G>A (p.Ala291Thr)	rs200267845	0.00012
NC_000002.11:g.(?_109336043)_(109579739_?)dup
NC_000002.11:g.(?_109367964)_(109579739_?)dup

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