ClinVar Miner

List of variants in gene combination FOXP1, LOC126806714 reported as likely pathogenic by MGZ Medical Genetics Center

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_001349338.3(FOXP1):c.1475A>G (p.Tyr492Cys)	rs2037702385
NM_001349338.3(FOXP1):c.1506C>G (p.Phe502Leu)	rs1057524152

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