List of variants in gene combination HPD, LOC126861662 reported as benign for tyrosinemia

Minimum submission review status:		Collection method:
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: 3

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HGVS	dbSNP	gnomAD frequency
NM_002150.3(HPD):c.294C>T (p.Phe98=)	rs117079110	0.00048
NM_002150.3(HPD):c.291G>A (p.Ala97=)	rs139901326	0.00017
NM_002150.3(HPD):c.324+20G>A	rs147479059

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