ClinVar Miner

List of variants in gene combination FOXP1, LOC126806714 reported by Breakthrough Genomics, Breakthrough Genomics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001349338.3(FOXP1):c.1530+157G>A	rs13068094	0.42179
NM_001349338.3(FOXP1):c.1530+45A>G	rs72960080	0.02685

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