ClinVar Miner

List of variants in gene combination DBNL, PGAM2 reported by Mayo Clinic Laboratories, Mayo Clinic

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000290.4(PGAM2):c.310GCC[1] (p.Ala105del)	rs769549607
NM_000290.4(PGAM2):c.635C>T (p.Thr212Met)
NM_000290.4(PGAM2):c.644C>A (p.Pro215His)	rs2128795523

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