List of variants reported as pathogenic for Fanconi anemia complementation group L by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_018062.4(FANCL):c.1007_1009del (p.Ile336_Cys337delinsSer)	rs747253294	0.00034
NM_018062.4(FANCL):c.1092G>A (p.Lys364=)	rs577063114	0.00002
NM_018062.4(FANCL):c.2T>C (p.Met1Thr)	rs761291501	0.00001

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