ClinVar Miner

List of variants in gene PHF6 reported as uncertain significance by Genetic Services Laboratory, University 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)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001015877.2(PHF6):c.927C>T (p.Asp309=)	rs112199174	0.00753
NM_001015877.2(PHF6):c.729+4A>G	rs188961105	0.00691

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