ClinVar Miner

List of variants in gene FGG reported as uncertain significance for coagulation protein disease

Included ClinVar conditions (43):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
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HGVS dbSNP
NM_000509.5(FGG):c.-53A>G rs886059156
NM_000509.5(FGG):c.1237A>G (p.Ile413Val) rs886059154
NM_000509.5(FGG):c.1285G>T (p.Gly429Trp) rs145938787
NM_000509.5(FGG):c.19C>T (p.Pro7Ser) rs374845868
NM_000509.5(FGG):c.502A>G (p.Thr168Ala) rs141559764
NM_000509.5(FGG):c.667-10G>C rs886059155
NM_021870.3(FGG):c.274C>T (p.Leu92Phe) rs142286849
NM_021870.3(FGG):c.309T>C (p.Asn103=) rs138916334

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