ClinVar Miner

List of variants in gene LOC130006883, SLC37A4 studied 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
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001164277.2(SLC37A4):c.-420G>C	rs2846281	0.80326
NM_001164277.2(SLC37A4):c.-384G>A	rs886047753
NM_001164277.2(SLC37A4):c.-439T>C	rs1943713097

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