List of variants in gene ACD reported as uncertain significance by Breakthrough Genomics, Breakthrough Genomics

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001082486.2(ACD):c.1178G>A (p.Arg393Lys)	rs531580930	0.00005
NM_001082486.2(ACD):c.617A>C (p.His206Pro)	rs755371076	0.00005
NM_001082486.2(ACD):c.1147C>T (p.Arg383Trp)	rs747913250	0.00001

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