List of variants in gene combination GGACT, PCCA 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001195087.2(GGACT):c.1904_1907del	rs200007489	0.01517
NM_001195087.2(GGACT):c.*1849G>A	rs41281122	0.00704
NM_001195087.2(GGACT):c.*1805A>C	rs113356477	0.00260
NM_001195087.2(GGACT):c.*1811dup	rs140492017

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