List of variants studied for Arterial calcification, generalized, of infancy, 2 by Baylor Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total variants: 5

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001171.6(ABCC6):c.3421C>T (p.Arg1141Ter)	rs72653706	0.00122
NM_001171.6(ABCC6):c.2787+1G>T	rs72664209	0.00017
NM_001171.6(ABCC6):c.469G>A (p.Gly157Arg)	rs1209940471	0.00003
NM_001171.6(ABCC6):c.1214C>T (p.Ala405Val)	rs115663615
NM_001171.6(ABCC6):c.3952G>A (p.Ala1318Thr)	rs2046496590

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.