Variants in gene PLCB1 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 16

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HGVS	dbSNP	gnomAD frequency
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.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.458A>T (p.Glu153Val)	rs45496299	0.00721
NM_015192.4(PLCB1):c.1167+7T>C	rs45466294	0.00492
NM_015192.4(PLCB1):c.1469A>G (p.Tyr490Cys)	rs45608240	0.00391
NM_015192.4(PLCB1):c.582T>C (p.Leu194=)	rs150770296	0.00354
NM_015192.4(PLCB1):c.3550C>T (p.Leu1184Phe)	rs28390202	0.00270
NM_015192.4(PLCB1):c.2673T>G (p.Pro891=)	rs142813933	0.00260
NM_015192.4(PLCB1):c.3120A>G (p.Gln1040=)	rs61755436	0.00213
NM_015192.4(PLCB1):c.639A>C (p.Arg213Ser)	rs140899287	0.00014

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