ClinVar Miner

List of variants in gene FGF10 reported as uncertain significance for EEC syndrome and related syndrome

Included ClinVar conditions (8):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
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HGVS dbSNP
NM_004465.1(FGF10):c.144G>A (p.Glu48=) rs886060655
NM_004465.1(FGF10):c.186C>A (p.Ser62Arg) rs886060654
NM_004465.1(FGF10):c.426C>T (p.Gly142=) rs149851674
NM_004465.1(FGF10):c.541A>C (p.Asn181His) rs1332768200
NM_004465.1(FGF10):c.624A>G (p.Ser208=) rs886060653

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