List of variants in gene FANCL reported as benign for Fanconi anemia complementation group L

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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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.375-49C>G	rs1404459	0.14499
NM_018062.4(FANCL):c.217-11T>C	rs79588315	0.06493
NM_018062.4(FANCL):c.1077T>C (p.Cys359=)	rs11539575	0.01385
NM_018062.4(FANCL):c.670A>G (p.Thr224Ala)	rs149731356	0.00355
NM_018062.4(FANCL):c.112C>T (p.Leu38Phe)	rs55849827	0.00322
NM_018062.4(FANCL):c.755T>G (p.Phe252Cys)	rs139801716	0.00004
NM_001114636.1(FANCL):c.-39A>G	rs41281511
NM_018062.4(FANCL):c.273+19dup	rs372101290

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