List of variants in gene PHYH reported as uncertain significance by GeneDx

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_006214.4(PHYH):c.244C>G (p.Arg82Gly)	rs145404396	0.00140
NM_006214.4(PHYH):c.601C>G (p.Arg201Gly)	rs143957922	0.00124
NM_006214.4(PHYH):c.606C>A (p.Asn202Lys)	rs201979258	0.00015
NM_006214.4(PHYH):c.354C>G (p.Ile118Met)	rs779724199	0.00005
NM_006214.4(PHYH):c.574G>A (p.Ala192Thr)	rs751660253	0.00005
NM_006214.4(PHYH):c.679G>C (p.Gly227Arg)	rs201936962
NM_006214.4(PHYH):c.760G>T (p.Asp254Tyr)	rs139329047
NM_006214.4(PHYH):c.856G>T (p.Asp286Tyr)	rs538686726

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