List of variants in gene PHYH studied for inborn disorder of amino acid metabolism

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_006214.4(PHYH):c.678+5G>T	rs201499815	0.00049
NM_006214.4(PHYH):c.135-2A>G	rs201578674	0.00017
NM_006214.4(PHYH):c.823C>T (p.Arg275Trp)	rs104894178	0.00007

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