ClinVar Miner

List of variants in gene combination ABHD14A-ACY1, ACY1 reported as uncertain significance by Neuberg Centre For Genomic Medicine, NCGM

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000666.3(ACY1):c.19G>A (p.Glu7Lys)	rs953420417	0.00001
NM_000666.3(ACY1):c.977C>G (p.Ala326Gly)	rs2471401082

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