List of variants reported as likely benign for Factor XII deficiency disease; Hereditary angioedema type 3 by Fulgent Genetics, Fulgent Genetics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000505.4(F12):c.398-12C>T	rs56285942	0.00495
NM_000505.4(F12):c.1272G>C (p.Thr424=)	rs61737766	0.00486
NM_000505.3(F12):c.-57G>C	rs41309132	0.00297
NM_000505.4(F12):c.-62C>T	rs187018744	0.00223

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