ClinVar Miner

List of variants in gene combination C2, CFB reported as benign for anemia (disease)

Included ClinVar conditions (263):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
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HGVS dbSNP
NM_000063.6(C2):c.1902+6G>C rs9332730
NM_001710.5(CFB):c.1365C>T (p.Val455=) rs2072634
NM_001710.5(CFB):c.450A>G (p.Arg150=) rs1048709
NM_001710.5(CFB):c.94C>T (p.Arg32Trp) rs12614
NM_001710.5(CFB):c.95G>A (p.Arg32Gln) rs641153

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