List of variants in gene ACD reported as benign for hematologic disorder

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: 17

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001082486.2(ACD):c.1295T>C (p.Val432Ala)	rs6979	0.60624
NM_001082486.2(ACD):c.1298+20C>A	rs67114979	0.13128
NM_001082486.2(ACD):c.413+3A>G	rs8058187	0.12302
NM_001082486.2(ACD):c.1371G>T (p.Pro457=)	rs14920	0.03535
NC_000016.10:g.67660703A>G	rs72547496	0.03001
NM_001082486.2(ACD):c.923G>A (p.Gly308Glu)	rs147189192	0.00679
NM_001082486.1(ACD):c.162C>T (p.Pro54=)	rs73597595	0.00544
NM_001082486.2(ACD):c.1207-10C>T	rs67185288	0.00536
NM_001082486.2(ACD):c.801C>T (p.Ala267=)	rs72549181	0.00530
NM_001082486.2(ACD):c.494-20C>T	rs59443695	0.00465
NM_001082486.2(ACD):c.819C>T (p.Pro273=)	rs138740815	0.00251
NM_001082486.2(ACD):c.1336C>T (p.Leu446=)	rs1050346	0.00188
NM_001082486.2(ACD):c.80G>A (p.Arg27Gln)	rs142507451	0.00135
NM_001082486.2(ACD):c.132C>T (p.Gly44=)	rs138527794	0.00102
NM_001082486.2(ACD):c.444C>T (p.Leu148=)	rs151132164	0.00096
NM_001082486.2(ACD):c.99+18G>A	rs369046068	0.00036
NM_001082486.2(ACD):c.743-3dup	rs1369632476

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.