List of variants in gene BAG3 reported as uncertain significance by Stanford Center for Inherited Cardiovascular Disease, Stanford University

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_004281.4(BAG3):c.1436C>T (p.Ala479Val)	rs34656239	0.00097
NM_004281.4(BAG3):c.280A>T (p.Ile94Phe)	rs145393807	0.00085
NM_004281.4(BAG3):c.653G>A (p.Arg218Gln)	rs201638005	0.00016
NM_004281.4(BAG3):c.554C>T (p.Ser185Leu)	rs730880054	0.00009
NM_004281.4(BAG3):c.616A>C (p.Ile206Leu)	rs199700646	0.00009
NM_004281.4(BAG3):c.133C>T (p.Arg45Cys)	rs747820097	0.00005
NM_004281.4(BAG3):c.322G>T (p.Val108Leu)	rs730880053
NM_004281.4(BAG3):c.784G>A (p.Ala262Thr)	rs876661343

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