List of variants in gene PLCB1 reported as benign by PreventionGenetics, part of Exact Sciences

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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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.1167+16G>A	rs2295179	0.57134
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.102C>T (p.Asp34=)	rs16994453	0.18027
NM_015192.4(PLCB1):c.1251-4T>G	rs2076689	0.09450
NM_015192.4(PLCB1):c.2082G>A (p.Gly694=)	rs3761170	0.05661
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.639A>C (p.Arg213Ser)	rs140899287	0.00014

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