List of variants in gene combination AP4M1, TAF6 reported as benign by Labcorp Genetics (formerly Invitae), Labcorp

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_139315.3(TAF6):c.1722C>T (p.Thr574=)	rs145939245	0.00509
NM_139315.3(TAF6):c.1539C>T (p.Ile513=)	rs114272994	0.00372
NM_139315.3(TAF6):c.1302T>C (p.Val434=)	rs140517175	0.00165
NM_139315.3(TAF6):c.1904C>T (p.Pro635Leu)	rs79147701	0.00121
NM_139315.3(TAF6):c.1899G>A (p.Ser633=)	rs143687621	0.00041
NM_139315.3(TAF6):c.1917C>T (p.Ser639=)	rs181717102	0.00038
NM_139315.3(TAF6):c.1806T>C (p.Ser602=)	rs201704839	0.00019

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