List of variants in gene BAG3 reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 18

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HGVS	dbSNP	gnomAD frequency
NM_004281.4(BAG3):c.180+43C>T	rs112546447	0.01071
NM_004281.4(BAG3):c.463G>A (p.Ala155Thr)	rs61756328	0.00239
NM_004281.4(BAG3):c.549C>G (p.Ser183=)	rs112929734	0.00141
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.870C>G (p.Pro290=)	rs140737221	0.00055
NM_004281.4(BAG3):c.855G>A (p.Thr285=)	rs147259596	0.00048
NM_004281.4(BAG3):c.821C>T (p.Ser274Leu)	rs143919208	0.00038
NM_004281.4(BAG3):c.381A>T (p.Ala127=)	rs140594879	0.00030
NM_004281.4(BAG3):c.771C>T (p.Pro257=)	rs200212999	0.00028
NM_004281.4(BAG3):c.645C>T (p.Asn215=)	rs138078305	0.00025
NM_004281.4(BAG3):c.415C>T (p.Arg139Trp)	rs556465096	0.00011
NM_004281.4(BAG3):c.636C>T (p.His212=)	rs150379892	0.00007
NM_004281.4(BAG3):c.1362C>T (p.Ile454=)	rs372417286	0.00006
NM_004281.4(BAG3):c.1281C>T (p.Ala427=)	rs748724796	0.00003
NM_004281.4(BAG3):c.705G>A (p.Ala235=)	rs141328836	0.00002
NM_004281.4(BAG3):c.372T>G (p.Thr124=)	rs766084373	0.00001
NM_004281.4(BAG3):c.255G>T (p.Val85=)

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