ClinVar Miner

List of variants in gene combination FANCL, VRK2 reported as benign for Fanconi anemia complementation group A

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
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HGVS dbSNP
NM_018062.3(FANCL):c.1077T>C (p.Cys359=) rs11539575
NM_018062.3(FANCL):c.1096_1099dup (p.Thr367fs) rs759217526
NM_018062.3(FANCL):c.755T>G (p.Phe252Cys) rs139801716
NM_018062.3(FANCL):c.817T>C (p.Leu273=) rs61753272
NM_018062.3(FANCL):c.981T>C (p.Ser327=) rs848291

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