ClinVar Miner

List of variants in gene combination FOXE3, LINC01389 reported as benign for anterior segment dysgenesis 1

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP
NM_012186.3(FOXE3):c.587G>C (p.Gly196Ala) rs281865461

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