List of variants in gene PHF6 reported as uncertain significance by Eurofins Ntd Llc (ga)

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001015877.2(PHF6):c.414C>T (p.Ser138=)	rs200423380	0.00011
NM_001015877.2(PHF6):c.688A>G (p.Ile230Val)	rs794727879	0.00002
NM_001015877.2(PHF6):c.706G>A (p.Ala236Thr)	rs794727878	0.00001
NM_001015877.2(PHF6):c.418+4C>T	rs794727736

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