List of variants reported as uncertain significance for Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency by Fulgent Genetics, Fulgent Genetics

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000500.9(CYP21A2):c.*13G>A	rs6447	0.01770
NM_000500.9(CYP21A2):c.1306C>T (p.Arg436Cys)	rs767333157	0.00075
NM_000500.9(CYP21A2):c.40G>T (p.Ala14Ser)	rs764636694	0.00023
NM_000500.9(CYP21A2):c.143A>G (p.Tyr48Cys)	rs566306310	0.00003
NM_000500.9(CYP21A2):c.738+75C>T	rs1463196531	0.00003

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