ClinVar Miner

List of variants in gene FANCF reported as benign for DNA repair disease

Included ClinVar conditions (124):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_022725.4(FANCF):c.*632G>A rs444923 0.97022
NM_022725.4(FANCF):c.*819C>T rs450946 0.96809
NM_022725.4(FANCF):c.*207C>T rs4447177 0.70234
NM_022725.4(FANCF):c.*1629C>T rs10500938 0.03856
NM_022725.4(FANCF):c.825G>A (p.Leu275=) rs36045913 0.01879
NM_022725.4(FANCF):c.*319A>G rs12294705 0.01761
NM_022725.4(FANCF):c.624G>T (p.Ala208=) rs7103674 0.01048
NM_022725.4(FANCF):c.*738T>G rs76674060 0.00915
NM_022725.4(FANCF):c.96C>T (p.Arg32=) rs151253274 0.00838
NM_022725.4(FANCF):c.*2123G>A rs45625034 0.00813
NM_022725.4(FANCF):c.387C>T (p.Leu129=) rs45556032 0.00759
NM_022725.4(FANCF):c.373G>A (p.Asp125Asn) rs61752920 0.00605
NM_022725.4(FANCF):c.557C>T (p.Ala186Val) rs113910234 0.00595
NM_022725.4(FANCF):c.*461G>T rs45458698 0.00359
NM_022725.4(FANCF):c.199A>C (p.Arg67=) rs146647469 0.00325
NM_022725.4(FANCF):c.*106T>C rs16909782 0.00215
NM_022725.4(FANCF):c.786A>G (p.Leu262=) rs11026706 0.00215
NM_022725.4(FANCF):c.246C>T (p.Asn82=) rs139724351 0.00185
NM_022725.4(FANCF):c.465A>T (p.Pro155=) rs201215734 0.00020
NM_022725.4(FANCF):c.148C>T (p.Arg50Trp) rs577253174 0.00006
NM_022725.4(FANCF):c.-10C>T rs3740615

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