List of variants in gene ACD reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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.1316T>C (p.Met439Thr)	rs202222217	0.00010
NM_001082486.2(ACD):c.493+7T>C	rs199626332	0.00008
NM_001082486.2(ACD):c.640del (p.Ala214fs)	rs2543603211

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