List of variants in gene PLCB4 reported as likely 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001377142.1(PLCB4):c.*563del	rs148015873	0.01013
NM_001377142.1(PLCB4):c.2525-8T>C	rs185755472	0.00039
NM_001377142.1(PLCB4):c.2046G>A (p.Ser682=)	rs200584230	0.00018
NM_001377142.1(PLCB4):c.1611+12C>T	rs761137370	0.00007
NM_001377142.1(PLCB4):c.936C>T (p.Tyr312=)	rs138780838	0.00004
NM_001377142.1(PLCB4):c.3408+11T>C	rs762636208	0.00003
NM_001377142.1(PLCB4):c.3133G>T (p.Ala1045Ser)	rs779018136	0.00002
NM_001377142.1(PLCB4):c.2566A>G (p.Ile856Val)	rs151284195	0.00001
NM_001377142.1(PLCB4):c.903C>T (p.Asn301=)	rs142446000	0.00001
NM_001377142.1(PLCB4):c.*1585dup	rs565091978

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