ClinVar Miner

List of variants in gene FGA reported as likely benign for coagulation protein disease

Included ClinVar conditions (43):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
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HGVS dbSNP
NM_021871.4(FGA):c.1199C>T (p.Ser400Phe) rs184635235
NM_021871.4(FGA):c.1444G>A (p.Val482Met) rs139146037
NM_021871.4(FGA):c.1542T>C (p.Pro514=) rs4766
NM_021871.4(FGA):c.1838A>G (p.His613Arg) rs201686865
NM_021871.4(FGA):c.904C>G (p.Pro302Ala) rs200203992

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