ClinVar Miner

List of variants in gene FGA reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (1030):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 4
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HGVS dbSNP
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.1823G>C (p.Gly608Ala) rs370873387
NM_021871.4(FGA):c.616C>G (p.Gln206Glu) rs560732073

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