List of variants in gene combination ABCC8, LOC110121471 reported as benign for disorder of glycolysis

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000352.6(ABCC8):c.2390+219T>C	rs4148632	0.89524
NM_000352.6(ABCC8):c.2390+123C>T	rs4148631	0.70926
NM_000352.6(ABCC8):c.2390+93C>T	rs4148630	0.70902
NM_000352.6(ABCC8):c.2391-17G>T	rs201484528	0.00206

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