ClinVar Miner

List of variants in gene combination FAM20A, PRKAR1A reported as benign for Carney complex, type 1

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 13
Download table as spreadsheet
HGVS dbSNP
NM_002734.5(PRKAR1A):c.*1057G>A
NM_002734.5(PRKAR1A):c.*2212C>T
NM_002734.5(PRKAR1A):c.*2844A>C
NM_212472.2(PRKAR1A):c.*1212T>G rs8905
NM_212472.2(PRKAR1A):c.*1244T>C rs9925
NM_212472.2(PRKAR1A):c.*1606A>G rs144632545
NM_212472.2(PRKAR1A):c.*1777C>T rs7977
NM_212472.2(PRKAR1A):c.*2188C>G rs6958
NM_212472.2(PRKAR1A):c.*587dup rs398041821
NM_212472.2(PRKAR1A):c.*672T>C rs546125048
NM_212472.2(PRKAR1A):c.*795G>T rs150031305
NM_212472.2(PRKAR1A):c.*870G>A rs8082254
NM_212472.2(PRKAR1A):c.1029C>T (p.Gly343=) rs1803241

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.