List of variants in gene ACD reported as uncertain significance by PreventionGenetics, part of Exact Sciences

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001082486.2(ACD):c.1063C>T (p.Pro355Ser)	rs757414908	0.00001
NM_001082486.2(ACD):c.751C>G (p.Leu251Val)	rs2052926994	0.00001
NM_001082486.2(ACD):c.862G>A (p.Glu288Lys)	rs200298308	0.00001
NM_001082486.2(ACD):c.-35C>T	rs895563147
NM_001082486.2(ACD):c.454C>T (p.Leu152Phe)	rs2543606711
NM_001082486.2(ACD):c.527G>T (p.Arg176Leu)	rs145007645

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