ClinVar Miner

List of variants in gene combination FOXE3, LINC01389 reported as likely benign by Eurofins NTD LLC (GA)

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 2
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HGVS dbSNP gnomAD frequency
NM_012186.3(FOXE3):c.16G>A (p.Asp6Asn) rs765169217 0.00868
NM_012186.3(FOXE3):c.898A>G (p.Ser300Gly) rs552420470 0.00350

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