ClinVar Miner

List of variants in gene FANCB reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (1030):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
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HGVS dbSNP
NM_001018113.3(FANCB):c.-232G>A rs756766337
NM_001018113.3(FANCB):c.1079C>T (p.Thr360Met) rs138192474
NM_001018113.3(FANCB):c.1105-26TATT[5] rs398123537
NM_001018113.3(FANCB):c.1349G>A (p.Cys450Tyr) rs764817410
NM_001018113.3(FANCB):c.1570C>G (p.Gln524Glu) rs370248837
NM_001018113.3(FANCB):c.1659G>A (p.Thr553=) rs767952529
NM_001018113.3(FANCB):c.1707A>G (p.Pro569=) rs1555904427
NM_001018113.3(FANCB):c.1769T>C (p.Phe590Ser) rs142959373
NM_001018113.3(FANCB):c.1817G>A (p.Ser606Asn) rs148560784
NM_001018113.3(FANCB):c.1838G>A (p.Arg613His) rs144764663
NM_001018113.3(FANCB):c.199A>G (p.Ile67Val) rs761346761
NM_001018113.3(FANCB):c.2342A>G (p.Glu781Gly) rs140363445
NM_001018113.3(FANCB):c.2379A>G (p.Gly793=) rs1374912480
NM_001018113.3(FANCB):c.2477C>T (p.Thr826Met) rs201436396
NM_001018113.3(FANCB):c.388A>G (p.Met130Val) rs776724055
NM_001018113.3(FANCB):c.402A>G (p.Leu134=) rs147260208
NM_001018113.3(FANCB):c.510T>G (p.Ile170Met) rs775216604
NM_001018113.3(FANCB):c.52T>C (p.Tyr18His) rs996732250
NM_001018113.3(FANCB):c.741C>A (p.Ile247=) rs760773732
NM_001018113.3(FANCB):c.7A>G (p.Ser3Gly) rs139111718
NM_001018113.3(FANCB):c.801A>C (p.Ser267=) rs773005941
NM_001018113.3(FANCB):c.884G>A (p.Gly295Glu) rs1270593506

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