List of variants reported as uncertain significance for Primary hyperoxaluria, type I by Counsyl

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000030.3(AGXT):c.866G>A (p.Arg289His)	rs61729604	0.00143
NM_000030.3(AGXT):c.*39G>A	rs369979466	0.00061
NM_000030.3(AGXT):c.865C>T (p.Arg289Cys)	rs180177290	0.00043
NM_000030.3(AGXT):c.145A>C (p.Met49Leu)	rs74205173	0.00022
NM_000030.3(AGXT):c.82C>T (p.Pro28Ser)	rs376684240	0.00006
NM_000030.3(AGXT):c.1072-91G>A	rs180177159
NM_000030.3(AGXT):c.260_271del (p.Glu87_Leu90del)	rs1553648333
NM_000030.3(AGXT):c.423G>C (p.Glu141Asp)	rs180177217
NM_000030.3(AGXT):c.683AGA[3] (p.Lys229dup)	rs1553648979
NM_000030.3(AGXT):c.781C>G (p.His261Asp)	rs778567956

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