ClinVar Miner

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

Included ClinVar conditions (262):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 19
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HGVS dbSNP
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.258C>A (p.Leu86=) rs146352365
NM_022725.3(FANCF):c.349C>A (p.Pro117Thr) rs372625322
NM_022725.3(FANCF):c.350C>T (p.Pro117Leu) rs374572943
NM_022725.3(FANCF):c.384A>C (p.Thr128=) rs200307118
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.672C>T (p.Pro224=) rs148955347
NM_022725.3(FANCF):c.687A>T (p.Ser229=) rs776140806
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.891T>G (p.Thr297=) rs1060504373
NM_022725.3(FANCF):c.90C>T (p.Thr30=) rs544395896
NM_022725.3(FANCF):c.96C>T (p.Arg32=) rs151253274
NM_022725.3(FANCF):c.993C>G (p.Thr331=) rs751274756

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