ClinVar Miner

List of variants in gene FANCE reported as likely benign for anemia (disease)

Included ClinVar conditions (258):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 18
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HGVS dbSNP
NM_021922.2(FANCE):c.*151A>G rs16876572
NM_021922.2(FANCE):c.-56C>T rs4713866
NM_021922.2(FANCE):c.1053T>G (p.Leu351=) rs755165473
NM_021922.2(FANCE):c.1071C>T (p.Leu357=) rs3823434
NM_021922.2(FANCE):c.1116C>T (p.Ile372=) rs143234424
NM_021922.2(FANCE):c.1316+10C>T rs200479051
NM_021922.2(FANCE):c.1383+10C>T rs1060504374
NM_021922.2(FANCE):c.1464C>T (p.Ala488=) rs779775366
NM_021922.2(FANCE):c.1509C>T (p.Asn503=) rs147166240
NM_021922.2(FANCE):c.1510-9T>C rs369210475
NM_021922.2(FANCE):c.210G>A (p.Glu70=) rs1008512809
NM_021922.2(FANCE):c.246G>A (p.Glu82=) rs769779495
NM_021922.2(FANCE):c.248+7C>A rs186563531
NM_021922.2(FANCE):c.284A>G (p.Gln95Arg) rs149097636
NM_021922.2(FANCE):c.561A>G (p.Glu187=) rs1554121329
NM_021922.2(FANCE):c.611C>T (p.Ser204Leu) rs7761870
NM_021922.2(FANCE):c.798G>A (p.Ser266=) rs746542545
NM_021922.2(FANCE):c.999C>T (p.Leu333=) rs776082827

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