List of variants in gene combination LOC130006147, PC 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001040716.2(PC):c.-282G>A	rs886048558	0.00026
NM_001040716.2(PC):c.-272G>A	rs927187081	0.00003

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