ClinVar Miner

List of variants in gene FANCL reported as benign for DNA repair disease

Included ClinVar conditions (106):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
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HGVS dbSNP
NM_001114636.1(FANCL):c.-39A>G rs41281511
NM_001114636.1(FANCL):c.108C>G (p.Phe36Leu) rs149726602
NM_001114636.1(FANCL):c.112C>T (p.Leu38Phe) rs55849827
NM_001114636.1(FANCL):c.217-11T>C rs79588315
NM_001114636.1(FANCL):c.402T>C (p.Ser134=) rs145284589
NM_001114636.1(FANCL):c.685A>G (p.Thr229Ala) rs149731356

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