List of variants in gene STAC3 reported as likely benign by GeneDx

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_145064.3(STAC3):c.670+33G>A	rs73120041	0.01315
NM_145064.3(STAC3):c.-1-123G>A	rs115674317	0.01282
NM_145064.3(STAC3):c.1086G>A (p.Glu362=)	rs61739642	0.01278
NM_145064.3(STAC3):c.432+143G>A	rs184042741	0.00883
NM_145064.3(STAC3):c.996+17A>T	rs150268069	0.00790
NM_145064.3(STAC3):c.720+44A>G	rs138487577	0.00787
NM_145064.3(STAC3):c.-1-201G>C	rs146782594	0.00560
NM_145064.3(STAC3):c.1023G>C (p.Ala341=)	rs61747067	0.00529
NM_145064.3(STAC3):c.432+97C>T	rs150491795	0.00452
NM_145064.3(STAC3):c.355C>T (p.Arg119Cys)	rs146313451	0.00132
NM_145064.3(STAC3):c.604-28G>A	rs372549290	0.00082
NM_145064.3(STAC3):c.433-180del	rs113333044
NM_145064.3(STAC3):c.433-183_433-180del	rs113333044
NM_145064.3(STAC3):c.604-165del	rs374655952
NM_145064.3(STAC3):c.604-167_604-165dup	rs374655952
NM_145064.3(STAC3):c.997-60_997-58del	rs141957095

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