List of variants in gene combination FAH, LOC112272621 reported as uncertain significance for Tyrosinemia type I

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000137.4(FAH):c.322A>G (p.Ile108Val)	rs747942022	0.00004
NM_000137.4(FAH):c.341C>T (p.Thr114Met)	rs772014160	0.00002
NM_000137.4(FAH):c.343A>G (p.Met115Val)
NM_000137.4(FAH):c.348C>A (p.His116Gln)

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