List of variants in gene combination FANCL, VRK2 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_018062.4(FANCL):c.*95A>G	rs76348639	0.00754
NM_006296.7(VRK2):c.102_105dup	rs759217526

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