List of variants in gene FANCL reported as pathogenic by CeGaT Center for Human Genetics Tuebingen

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.2T>C (p.Met1Thr)	rs761291501	0.00001
NM_018062.4(FANCL):c.739_740dup (p.Met247fs)	rs1685514075
NM_018062.4(FANCL):c.932dup (p.Tyr311Ter)	rs529201454

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