List of variants in gene ACD reported as not provided

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_001082486.2(ACD):c.1295T>C (p.Val432Ala)	rs6979	0.60624
NM_001082486.2(ACD):c.22G>A (p.Val8Ile)	rs149365469	0.00053
NM_001082486.2(ACD):c.1213C>A (p.Pro405Thr)	rs201441120	0.00002
NM_001082486.2(ACD):c.250_252del (p.Lys84del)	rs797045144

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