List of variants in gene CLEC7A reported as uncertain significance 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_197947.3(CLEC7A):c.414A>G (p.Leu138=)	rs143893294	0.00029
NM_197947.3(CLEC7A):c.536T>C (p.Phe179Ser)	rs1948157159

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