List of variants in gene PHF6 reported as not provided

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001015877.2(PHF6):c.487C>T (p.Arg163Cys)	rs199945885	0.00007
NM_001015877.2(PHF6):c.233C>T (p.Thr78Met)	rs767406620	0.00001
NM_001015877.2(PHF6):c.527C>T (p.Ser176Leu)	rs587778604

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