List of variants in gene PYGM reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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_005609.4(PYGM):c.1237A>T (p.Asn413Tyr)	rs142054672	0.00157
NM_005609.4(PYGM):c.160T>G (p.Phe54Val)	rs148839812	0.00046
NM_005609.4(PYGM):c.2300T>C (p.Met767Thr)

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