ClinVar Miner

List of variants in gene combination FANCL, VRK2 reported as likely pathogenic for anemia (disease)

Included ClinVar conditions (262):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
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NM_018062.3(FANCL):c.1007_1009del (p.Ile336_Cys337delinsSer) rs747253294
NM_018062.3(FANCL):c.1049_1050AG[1] (p.Ser351fs) rs750871999
NM_018062.3(FANCL):c.1092+1_1092+5delGTAAG rs1558727300
NM_018062.3(FANCL):c.692-2A>G rs1558737575

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