ClinVar Miner

List of variants in gene combination LOC130006883, SLC37A4 reported as uncertain significance for Glycogen storage disease, type I

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001164277.2(SLC37A4):c.-384G>A	rs886047753
NM_001164277.2(SLC37A4):c.-439T>C	rs1943713097

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