List of variants in gene PLCB1 reported as benign by Athena Diagnostics Inc

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: 13

Download table as spreadsheet

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.1251-4T>G	rs2076689	0.09450
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.2191C>G (p.Pro731Ala)	rs61755434	0.00997
NM_015192.4(PLCB1):c.2413+9C>T	rs138442805	0.00934
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.3120A>G (p.Gln1040=)	rs61755436	0.00213

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.