List of variants in gene BAG3 reported as likely benign by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

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_004281.4(BAG3):c.231G>A (p.Pro77=)	rs143752613	0.00441
NM_004281.4(BAG3):c.181-9T>A	rs139232658	0.00317
NM_004281.4(BAG3):c.-17G>A	rs200388926	0.00218
NM_004281.4(BAG3):c.1587C>T (p.Ala529=)	rs149358702	0.00144
NM_004281.4(BAG3):c.549C>G (p.Ser183=)	rs112929734	0.00141
NM_004281.4(BAG3):c.280A>T (p.Ile94Phe)	rs145393807	0.00085
NM_004281.4(BAG3):c.855G>A (p.Thr285=)	rs147259596	0.00048
NM_004281.4(BAG3):c.888C>T (p.His296=)	rs139399890	0.00040
NM_004281.4(BAG3):c.230C>T (p.Pro77Leu)	rs141355480	0.00033
NM_004281.4(BAG3):c.771C>T (p.Pro257=)	rs200212999	0.00028
NM_004281.4(BAG3):c.1240G>A (p.Glu414Lys)	rs117749531	0.00024
NM_004281.4(BAG3):c.96G>T (p.Pro32=)	rs372083121	0.00017
NM_004281.4(BAG3):c.483G>A (p.Gln161=)	rs758279156	0.00003
NM_004281.4(BAG3):c.828G>A (p.Arg276=)	rs752538980	0.00001
NM_004281.4(BAG3):c.212G>A (p.Arg71Gln)	rs35434411
NM_004281.4(BAG3):c.528C>T (p.Ala176=)	rs796123466

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