ClinVar Miner

List of variants reported as pathogenic for Fanconi anemia complementation group L by Baylor Genetics

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_018062.4(FANCL):c.1092G>A (p.Lys364=)	rs577063114	0.00002
NM_018062.4(FANCL):c.217-2A>G
NM_018062.4(FANCL):c.430del (p.Ser144fs)	rs869320685

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