List of variants in gene PLCG2 reported as likely pathogenic for immune system disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_002661.5(PLCG2):c.2095G>A (p.Gly699Ser)	rs753618006	0.00003
NM_002661.5(PLCG2):c.1993C>T (p.Arg665Trp)	rs1057519831
NM_002661.5(PLCG2):c.2535A>C (p.Leu845Phe)	rs1057519832
NM_002661.5(PLCG2):c.2535A>T (p.Leu845Phe)	rs1057519832
NM_002661.5(PLCG2):c.3420T>A (p.Asp1140Glu)

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