List of variants in gene PLCB1 reported as benign by Genetic Services Laboratory, University of Chicago

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_015192.4(PLCB1):c.3188+8C>T	rs2327089	0.89617
NM_015192.4(PLCB1):c.2988T>C (p.Ala996=)	rs2235613	0.62539
NM_015192.4(PLCB1):c.3337C>T (p.Leu1113=)	rs2294597	0.24864
NM_015192.4(PLCB1):c.2565G>A (p.Ala855=)	rs2076413	0.24634
NM_015192.4(PLCB1):c.99+8T>C	rs6086350	0.04369
NM_015192.4(PLCB1):c.3202T>C (p.Leu1068=)	rs41275588	0.03299
NM_015192.4(PLCB1):c.924A>G (p.Ser308=)	rs6056003	0.01487
NM_015192.4(PLCB1):c.2967G>A (p.Thr989=)	rs45464693	0.00730
NM_015192.4(PLCB1):c.458A>T (p.Glu153Val)	rs45496299	0.00721
NM_015192.4(PLCB1):c.1167+7T>C	rs45466294	0.00492
NM_015192.4(PLCB1):c.582T>C (p.Leu194=)	rs150770296	0.00354
NM_015192.4(PLCB1):c.3120A>G (p.Gln1040=)	rs61755436	0.00213

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