ClinVar Miner

List of variants in gene FOXG1 reported as uncertain significance by Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_005249.5(FOXG1):c.271C>A (p.Pro91Thr)	rs1555321245	0.00002
NM_005249.5(FOXG1):c.1123G>A (p.Ala375Thr)	rs1594384127	0.00001

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