List of variants in gene FANCL reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_018062.4(FANCL):c.981T>C (p.Ser327=)	rs848291	0.69782
NM_018062.4(FANCL):c.375-2014T>C	rs12475594	0.22541
NM_018062.4(FANCL):c.776-10dup	rs374236117

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