List of variants in gene PLCG2 reported as benign by CeGaT Center for Human Genetics Tuebingen

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_002661.5(PLCG2):c.82A>T (p.Met28Leu)	rs61749044	0.00973
NM_002661.5(PLCG2):c.1712A>G (p.Asn571Ser)	rs75472618	0.00802
NM_002661.5(PLCG2):c.1146T>C (p.Phe382=)	rs138637229	0.00731
NM_002661.5(PLCG2):c.1444T>C (p.Tyr482His)	rs187956469	0.00341
NM_002661.5(PLCG2):c.2355C>T (p.Ser785=)	rs185307548	0.00307
NM_002661.5(PLCG2):c.2324A>G (p.Lys775Arg)	rs142825971	0.00204
NM_002661.5(PLCG2):c.3671G>A (p.Arg1224His)	rs370547009	0.00074
NM_002661.5(PLCG2):c.3112C>T (p.Leu1038=)	rs200813182	0.00067
NM_002661.5(PLCG2):c.2393A>G (p.Asn798Ser)	rs117077093	0.00061
NM_002661.5(PLCG2):c.77C>T (p.Thr26Met)	rs189301790	0.00058
NM_002661.5(PLCG2):c.57G>A (p.Lys19=)	rs369542354	0.00055
NM_002661.5(PLCG2):c.1959C>T (p.Arg653=)	rs117835631	0.00035
NM_002661.5(PLCG2):c.1073-8C>G	rs372603106	0.00004
NM_002661.5(PLCG2):c.540C>G (p.Ala180=)	rs150276286

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