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

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_145861.4(EDARADD):c.*1072C>T	rs988277282	0.00039
NM_022336.4(EDAR):c.259T>C (p.Cys87Arg)	rs121908451	0.00001
NM_022336.4(EDAR):c.1057C>T (p.Leu353Phe)
NM_145861.4(EDARADD):c.*1962C>T	rs111987152
NM_145861.4(EDARADD):c.*558C>T	rs1309549108

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