List of variants studied 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_022336.4(EDAR):c.1109T>C (p.Val370Ala)	rs3827760	0.07017
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
NM_022336.4(EDAR):c.77C>T (p.Ala26Val)	rs550414401	0.00004
NC_000002.11:g.(?_109336043)_(109579739_?)dup
NC_000002.11:g.(?_109367964)_(109579739_?)dup

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