ClinVar Miner

List of variants in gene combination FANCL, VRK2 reported as likely benign for Fanconi anemia

Included ClinVar conditions (38):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
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HGVS dbSNP
NM_018062.3(FANCL):c.1021-6T>C rs377052216
NM_018062.3(FANCL):c.1115G>C (p.Gly372Ala) rs149803148
NM_018062.3(FANCL):c.693T>G (p.Gly231=) rs864622189
NM_018062.3(FANCL):c.705C>T (p.Ser235=) rs1553435677
NM_018062.3(FANCL):c.846A>G (p.Gln282=) rs535158133
NM_018062.3(FANCL):c.918T>C (p.Asp306=) rs1060504376
NM_018062.3(FANCL):c.963T>A (p.Asp321Glu) rs140088149

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