List of variants in gene CALCRL reported as benign for immune system disorder

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_005795.6(CALCRL):c.782-58T>C	rs1706287	0.87308
NM_005795.6(CALCRL):c.1128+34A>G	rs858745	0.87294

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