List of variants reported as pathogenic for Reticular dysgenesis by Labcorp Genetics (formerly Invitae), Labcorp

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001625.4(AK2):c.498+1G>A	rs777503956	0.00003
NM_001625.4(AK2):c.409C>T (p.Arg137Ter)	rs1476680673	0.00001
NC_000001.10:g.(?_33473829)_(33478866_?)del
NC_000001.10:g.(?_33480103)_(33480215_?)del
NC_000001.10:g.(?_33490023)_(33502429_?)del
NM_001625.4(AK2):c.307C>T (p.Arg103Trp)	rs267606648
NM_001625.4(AK2):c.330+5G>A	rs1569646997
NM_001625.4(AK2):c.374_375del (p.Val125fs)	rs2522072280
NM_001625.4(AK2):c.494A>G (p.Asp165Gly)	rs267606643
NM_001625.4(AK2):c.597_599dup (p.Tyr200Ter)	rs2124279569
NM_001625.4(AK2):c.84dup (p.Gly29fs)	rs1640610158

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.