List of variants in gene BAG3 reported as benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_004281.4(BAG3):c.1296A>G (p.Val432=)	rs196295	0.75935
NM_004281.4(BAG3):c.451T>C (p.Cys151Arg)	rs2234962	0.14532
NM_004281.4(BAG3):c.1220C>T (p.Pro407Leu)	rs3858340	0.12393
NM_004281.4(BAG3):c.1002T>G (p.Pro334=)	rs3858339	0.12375
NM_004281.4(BAG3):c.231G>A (p.Pro77=)	rs143752613	0.00441
NM_004281.4(BAG3):c.249C>A (p.His83Gln)	rs151331972	0.00344
NM_004281.4(BAG3):c.606G>T (p.Pro202=)	rs74157690	0.00341
NM_004281.4(BAG3):c.187C>G (p.Pro63Ala)	rs144041999	0.00328
NM_004281.4(BAG3):c.1138C>T (p.Pro380Ser)	rs144692954	0.00327
NM_004281.4(BAG3):c.181-9T>A	rs139232658	0.00317
NM_004281.4(BAG3):c.1587C>T (p.Ala529=)	rs149358702	0.00144
NM_004281.3(BAG3):c.772C>T (p.Arg258Trp)	rs117671123	0.00036
NM_004281.4(BAG3):c.212G>A (p.Arg71Gln)	rs35434411
NM_004281.4(BAG3):c.468GGC[4] (p.Ala160dup)	rs139438727

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