List of variants in gene CEL 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001807.6(CEL):c.1454T>C (p.Ile485Thr)	rs77696629	0.02562
NM_001807.6(CEL):c.353T>G (p.Leu118Arg)	rs113056079	0.01720
NM_001807.6(CEL):c.402C>G (p.Gly134=)	rs150358550	0.00392
NM_001807.6(CEL):c.1485-8C>T	rs185188893	0.00072
NM_001807.6(CEL):c.1659C>G (p.Thr553=)	rs78256304

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