List of variants in gene combination AP4M1, TAF6 reported as likely benign 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
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_004722.4(AP4M1):c.*387C>T	rs146348021	0.00325
NM_139315.3(TAF6):c.1770C>T (p.Thr590=)	rs145591068	0.00050
NM_139315.3(TAF6):c.1710C>T (p.Pro570=)	rs138356641	0.00006

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