List of variants reported as uncertain significance for galactosemia by Fulgent Genetics, Fulgent Genetics

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000155.4(GALT):c.1132A>G (p.Ile378Val)	rs111033819	0.00014
NM_001008216.2(GALE):c.307G>T (p.Asp103Tyr)	rs542486536	0.00006
NM_000155.4(GALT):c.611G>A (p.Arg204Gln)	rs111033740	0.00005
NM_001008216.2(GALE):c.506G>A (p.Arg169Gln)	rs140878602	0.00005
NM_001008216.2(GALE):c.878C>T (p.Pro293Leu)	rs775072430	0.00002
NM_000155.4(GALT):c.1034C>A (p.Ala345Asp)	rs111033815	0.00001
NM_000155.4(GALT):c.203A>G (p.His68Arg)	rs193922247
NM_000155.4(GALT):c.286G>C (p.Asp96His)

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