List of variants in gene PLCG2 reported as uncertain significance by Baylor Genetics

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.923C>T (p.Ala308Val)	rs199636472	0.00104
NM_002661.5(PLCG2):c.564+19C>T	rs564767670	0.00004
NM_002661.5(PLCG2):c.3755G>C (p.Arg1252Thr)	rs748492148	0.00002
NM_002661.5(PLCG2):c.3098G>A (p.Arg1033His)	rs760293225	0.00001
NM_002661.5(PLCG2):c.337+2T>C	rs866001196	0.00001
NM_002661.5(PLCG2):c.146C>T (p.Thr49Met)
NM_002661.5(PLCG2):c.1868G>T (p.Arg623Leu)	rs1909580178
NM_002661.5(PLCG2):c.899G>T (p.Ser300Ile)	rs764885126
NM_002661.5(PLCG2):c.906G>C (p.Trp302Cys)	rs1908633748

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