ClinVar Miner

List of variants in gene PLCG2 studied for B-cell neoplasm

Included ClinVar conditions (16):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
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

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