ClinVar Miner

List of variants in gene FGG reported as uncertain significance by NIHR Bioresource Rare Diseases, University of Cambridge

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 5
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HGVS dbSNP gnomAD frequency
NM_021870.3(FGG):c.571G>A (p.Gly191Arg) rs6063 0.00339
NM_021870.3(FGG):c.447C>A (p.Asn149Lys) rs751435976 0.00004
NM_021870.3(FGG):c.185T>C (p.Val62Ala) rs1578812818
NM_021870.3(FGG):c.622T>C (p.Cys208Arg) rs1578810954
NM_021870.3(FGG):c.952G>A (p.Gly318Ser) rs267606810

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