List of variants in gene PHF6 reported as likely benign by Ambry Genetics

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001015877.2(PHF6):c.123G>A (p.Ala41=)	rs573685409	0.00004
NM_001015877.2(PHF6):c.648T>C (p.His216=)	rs755211450	0.00004
NM_001015877.2(PHF6):c.274A>G (p.Ile92Val)	rs773176481	0.00002
NM_001015877.2(PHF6):c.159A>G (p.Val53=)	rs769976257	0.00001
NM_001015877.2(PHF6):c.762A>C (p.Thr254=)	rs754317008	0.00001
NM_001015877.2(PHF6):c.1089T>C (p.Asn363=)	rs2520676263
NM_001015877.2(PHF6):c.525G>C (p.Leu175=)	rs1383351397

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