ClinVar Miner

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

Included ClinVar conditions (263):
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Gene type:
ClinVar version:
Total variants: 16
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HGVS dbSNP
NM_022725.3(FANCF):c.*207C>T rs4447177
NM_022725.3(FANCF):c.*632G>A rs444923
NM_022725.3(FANCF):c.*819C>T rs450946
NM_022725.3(FANCF):c.-10C>T rs3740615
NM_022725.3(FANCF):c.199A>C (p.Arg67=) rs146647469
NM_022725.3(FANCF):c.246C>T (p.Asn82=) rs139724351
NM_022725.3(FANCF):c.373G>A (p.Asp125Asn) rs61752920
NM_022725.3(FANCF):c.387C>T (p.Leu129=) rs45556032
NM_022725.3(FANCF):c.465A>T (p.Pro155=) rs201215734
NM_022725.3(FANCF):c.557C>T (p.Ala186Val) rs113910234
NM_022725.3(FANCF):c.624G>T (p.Ala208=) rs7103674
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.883G>A (p.Val295Ile) rs7103293
NM_022725.3(FANCF):c.959C>T (p.Pro320Leu) rs45451294
NM_022725.3(FANCF):c.96C>T (p.Arg32=) rs151253274

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