List of variants in gene PLCG2 reported as benign by Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_002661.5(PLCG2):c.2055-8T>C	rs12448130	0.99106
NM_002661.5(PLCG2):c.1497C>T (p.Ala499=)	rs1143689	0.73561
NM_002661.5(PLCG2):c.432-13T>A	rs4888183	0.55511
NM_002661.5(PLCG2):c.2236-14C>G	rs12446127	0.48966
NM_002661.5(PLCG2):c.3093T>C (p.Asn1031=)	rs1071644	0.39075
NM_002661.5(PLCG2):c.1149C>T (p.Asp383=)	rs1143688	0.33340
NM_002661.5(PLCG2):c.297A>G (p.Leu99=)	rs1143686	0.26621
NM_002661.5(PLCG2):c.1188C>G (p.Thr396=)	rs13333716	0.06533
NM_002661.5(PLCG2):c.731A>G (p.His244Arg)	rs11548656	0.02717
NM_002661.5(PLCG2):c.770A>T (p.His257Leu)	rs45443101	0.02615
NM_002661.5(PLCG2):c.82A>T (p.Met28Leu)	rs61749044	0.00973

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