List of variants in gene PLCG2 reported as likely benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_002661.5(PLCG2):c.3414A>G (p.Glu1138=)	rs61755443	0.00247
NM_002661.5(PLCG2):c.714C>T (p.Ala238=)	rs138981519	0.00237
NM_002661.5(PLCG2):c.2324A>G (p.Lys775Arg)	rs142825971	0.00204
NM_002661.5(PLCG2):c.771T>C (p.His257=)	rs369555285	0.00091
NM_002661.5(PLCG2):c.171C>T (p.Thr57=)	rs374354863	0.00019
NM_002661.5(PLCG2):c.2211C>T (p.Pro737=)	rs368933697	0.00019
NM_002661.5(PLCG2):c.2121C>T (p.Ser707=)	rs527809751	0.00003
NM_002661.5(PLCG2):c.3657A>T (p.Thr1219=)	rs201318091	0.00003
NM_002661.5(PLCG2):c.3198+6G>A	rs752647511

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