List of variants in gene BAG3 reported as likely benign by Illumina Laboratory Services, Illumina

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.*31C>T	rs116329258	0.00853
NM_004281.4(BAG3):c.231G>A (p.Pro77=)	rs143752613	0.00441
NM_004281.4(BAG3):c.606G>T (p.Pro202=)	rs74157690	0.00341
NM_004281.4(BAG3):c.*267C>A	rs552025009	0.00153
NM_004281.3(BAG3):c.772C>T (p.Arg258Trp)	rs117671123	0.00036
NM_004281.4(BAG3):c.898G>A (p.Asp300Asn)	rs78439745	0.00026
NM_004281.4(BAG3):c.1674G>A (p.Ala558=)	rs142981190	0.00021
NM_004281.4(BAG3):c.1321A>G (p.Asn441Asp)	rs201181493	0.00011
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.-18G>A	rs754210695	0.00006
NM_004281.4(BAG3):c.-4C>T	rs727502894	0.00006
NM_004281.4(BAG3):c.1214C>T (p.Ala405Val)	rs11199064	0.00006
NM_004281.4(BAG3):c.693G>A (p.Thr231=)	rs144034433	0.00006
NM_004281.4(BAG3):c.212G>A (p.Arg71Gln)	rs35434411
NM_004281.4(BAG3):c.468GGC[4] (p.Ala160dup)	rs139438727

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