List of variants in gene PLCB4 reported as uncertain significance for auriculocondylar syndrome 1

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001377142.1(PLCB4):c.*469G>T	rs886056986	0.00005
NM_001377142.1(PLCB4):c.*1672del	rs886056991
NM_001377142.1(PLCB4):c.3409-4del	rs886056984
NM_001377142.1(PLCB4):c.3496-5_3496-2del	rs886056985

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