ClinVar Miner

List of variants in gene IFRD1 reported as likely benign by Breakthrough Genomics, Breakthrough Genomics

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001550.4(IFRD1):c.200-14A>C	rs11773535	0.02279
NM_001550.4(IFRD1):c.568-10T>A	rs565300368	0.00121

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