List of variants in gene ISCU reported as benign for hereditary myopathy with lactic acidosis due to ISCU deficiency

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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_213595.4(ISCU):c.20T>G (p.Phe7Cys)	rs10778648	0.86086
NM_213595.4(ISCU):c.19T>G (p.Phe7Val)	rs10778647	0.86084
NM_213595.4(ISCU):c.35C>T (p.Ala12Val)	rs2287555	0.56452
NM_213595.4(ISCU):c.19_20delinsGG (p.Phe7Gly)	rs67681514

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