List of variants reported as uncertain significance for RFT1-congenital disorder of glycosylation by Revvity Omics, Revvity

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_052859.4(RFT1):c.826+7T>C	rs192264403	0.00103
NM_052859.4(RFT1):c.1331C>T (p.Thr444Met)	rs147740901	0.00039
NM_052859.4(RFT1):c.698C>T (p.Ala233Val)	rs751030368	0.00001
NM_052859.4(RFT1):c.1459-2A>G

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