List of variants in gene PLCB1 reported as benign by Illumina Laboratory Services, Illumina

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_015192.4(PLCB1):c.3188+8C>T	rs2327089	0.89617
NM_015192.4(PLCB1):c.*1681T>C	rs1047381	0.74584
NM_015192.4(PLCB1):c.2988T>C (p.Ala996=)	rs2235613	0.62539
NM_015192.4(PLCB1):c.*2510C>T	rs1047383	0.55952
NM_015192.4(PLCB1):c.3337C>T (p.Leu1113=)	rs2294597	0.24864
NM_015192.4(PLCB1):c.3202T>C (p.Leu1068=)	rs41275588	0.03299
NM_015192.4(PLCB1):c.*1551A>G	rs77690948	0.01631
NM_015192.4(PLCB1):c.2199G>A (p.Val733=)	rs8118206	0.01438
NM_015192.4(PLCB1):c.458A>T (p.Glu153Val)	rs45496299	0.00721
NM_015192.4(PLCB1):c.3120A>G (p.Gln1040=)	rs61755436	0.00213
NM_015192.4(PLCB1):c.*1707A>G	rs708910

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