List of variants in gene combination HPD, LOC130009013 reported as uncertain significance for inborn disorder of amino acid metabolism

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_002150.3(HPD):c.*191C>T	rs886049036	0.00038
NM_002150.3(HPD):c.*65A>G	rs931600760	0.00007
NM_002150.2(HPD):c.*202T>A	rs1352129485	0.00002
NM_002150.3(HPD):c.*190G>T	rs942325148
NM_002150.3(HPD):c.*69C>T	rs1592913492
NM_002150.3(HPD):c.*82T>C	rs879205776

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