List of variants in gene combination DBNL, LOC129998342, PGAM2 reported as uncertain significance for carbohydrate metabolism disease

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000290.4(PGAM2):c.365C>T (p.Pro122Leu)	rs147273213	0.00002
NM_000290.4(PGAM2):c.374C>T (p.Pro125Leu)	rs1385458139	0.00001
NM_000290.4(PGAM2):c.350G>A (p.Arg117His)
NM_000290.4(PGAM2):c.359A>G (p.Asp120Gly)
NM_000290.4(PGAM2):c.368C>G (p.Pro123Arg)	rs372435680
NM_000290.4(PGAM2):c.368C>T (p.Pro123Leu)

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