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: 6
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NM_001114636.1(FANCL):c.1092T>C (p.Cys364=) rs11539575
NM_001114636.1(FANCL):c.1111_1114dup (p.Thr372fs) rs759217526
NM_001114636.1(FANCL):c.770T>G (p.Phe257Cys) rs139801716
NM_001114636.1(FANCL):c.832T>C (p.Leu278=) rs61753272
NM_001114636.1(FANCL):c.996T>C (p.Ser332=) rs848291
NM_018062.4(FANCL):c.739A>G (p.Met247Val) rs561027973

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