ClinVar Miner

List of variants in gene PGM1 reported as likely pathogenic by Labcorp Genetics (formerly Invitae), Labcorp

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_002633.3(PGM1):c.871G>A (p.Gly291Arg)	rs772768778	0.00003
NM_002633.3(PGM1):c.1281-2A>G	rs1649810314

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