ClinVar Miner

List of variants in gene FANCB reported as likely 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: 7
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NM_001018113.2(FANCB):c.127T>A (p.Leu43Ile) rs771007866
NM_001018113.2(FANCB):c.1349G>A (p.Cys450Tyr) rs764817410
NM_001018113.2(FANCB):c.1659G>A (p.Thr553=) rs767952529
NM_001018113.2(FANCB):c.1707A>G (p.Pro569=) rs1555904427
NM_001018113.2(FANCB):c.2394C>T (p.Val798=) rs190579053
NM_001018113.2(FANCB):c.2477C>T (p.Thr826Met) rs201436396
NM_001018113.2(FANCB):c.741C>A (p.Ile247=) rs760773732

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