List of variants reported as uncertain significance for Homocystinuria due to methylene tetrahydrofolate reductase deficiency; Neural tube defects, folate-sensitive; Schizophrenia; Thrombophilia due to thrombin defect by Fulgent Genetics, Fulgent Genetics

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_005957.5(MTHFR):c.1556G>T (p.Arg519Leu)	rs45449298	0.00118
NM_005957.5(MTHFR):c.203G>A (p.Arg68Gln)	rs2066472	0.00031
NM_005957.5(MTHFR):c.673A>G (p.Ile225Val)	rs200100285	0.00028
NM_005957.5(MTHFR):c.1720G>A (p.Val574Ile)	rs202153689	0.00015
NM_005957.5(MTHFR):c.151C>T (p.Arg51Trp)	rs764131110	0.00003
NM_005957.5(MTHFR):c.1064C>T (p.Pro355Leu)	rs794727869

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