List of variants in gene ISCU reported as benign for not specified

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)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_213595.4(ISCU):c.27G>T (p.Leu9=)	rs11837563	0.02615
NM_213595.4(ISCU):c.51G>A (p.Leu17=)	rs112552261	0.00804
NM_213595.4(ISCU):c.52C>A (p.Leu18Met)	rs142514490	0.00291
NM_213595.4(ISCU):c.229-5T>C	rs761922921	0.00014
NM_213595.4(ISCU):c.*14G>A	rs199557747	0.00012
NM_213595.4(ISCU):c.339+6dup	rs863224043

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