ClinVar Miner

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

Included ClinVar conditions (87):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
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NM_001114636.1(FANCL):c.*333A>G rs147811379
NM_001114636.1(FANCL):c.1036-6T>C rs377052216
NM_001114636.1(FANCL):c.1130G>C (p.Gly377Ala) rs149803148
NM_001114636.1(FANCL):c.720C>T (p.Ser240=) rs1553435677
NM_001114636.1(FANCL):c.832T>C (p.Leu278=) rs61753272
NM_001114636.1(FANCL):c.861A>G (p.Gln287=) rs535158133
NM_001114636.1(FANCL):c.933T>C (p.Asp311=) rs1060504376
NM_001114636.1(FANCL):c.978T>A (p.Asp326Glu) rs140088149
NM_018062.4(FANCL):c.776-8A>T rs753745302

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