ClinVar Miner

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

Included ClinVar conditions (956):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
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NM_022725.3(FANCF):c.*106T>C rs16909782
NM_022725.3(FANCF):c.*1629C>T rs10500938
NM_022725.3(FANCF):c.*319A>G rs12294705
NM_022725.3(FANCF):c.1035C>T (p.Ser345=) rs1554963603
NM_022725.3(FANCF):c.600C>T (p.Asn200=) rs143713546
NM_022725.3(FANCF):c.640T>C (p.Leu214=) rs773556058
NM_022725.3(FANCF):c.786A>G (p.Leu262=) rs11026706
NM_022725.3(FANCF):c.825G>A (p.Leu275=) rs36045913
NM_022725.3(FANCF):c.885T>G (p.Val295=) rs761238804
NM_022725.3(FANCF):c.96C>T (p.Arg32=) rs151253274
NM_022725.3(FANCF):c.993C>G (p.Thr331=) rs751274756

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