ClinVar Miner

List of variants in gene combination FOXE3, LINC01389 reported as pathogenic for cataract

Included ClinVar conditions (65):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 4
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HGVS dbSNP gnomAD frequency
NM_012186.3(FOXE3):c.307G>A (p.Glu103Lys) rs1057518738 0.00003
NM_012186.3(FOXE3):c.351C>G (p.Asn117Lys) rs1057518737
NM_012186.3(FOXE3):c.958T>C (p.Ter320Arg) rs2124045186
NM_012186.3(FOXE3):c.959G>C (p.Ter320Ser) rs387906793

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