rs16835979, STX18-AS1

N. diseases: 6
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Congenital heart disease
CUI: C0152021
Disease: Congenital heart disease
80 0.851 0.120 4 4633549 intron variant C/A snv 0.20 0.710 1.000 2 2013 2015
Atrial Septal Defects
CUI: C0018817
Disease: Atrial Septal Defects
96 0.851 0.120 4 4633549 intron variant C/A snv 0.20 0.030 1.000 3 2014 2016
ATRIAL SEPTAL DEFECT 1
CUI: C1862389
Disease: ATRIAL SEPTAL DEFECT 1
16 0.851 0.120 4 4633549 intron variant C/A snv 0.20 0.020 1.000 2 2014 2016
Autism Spectrum Disorders
CUI: C1510586
Disease: Autism Spectrum Disorders
331 0.851 0.120 4 4633549 intron variant C/A snv 0.20 0.020 1.000 2 2014 2016
Ostium secundum atrial septal defect
CUI: C0344724
Disease: Ostium secundum atrial septal defect
10 0.851 0.120 4 4633549 intron variant C/A snv 0.20 0.020 1.000 2 2014 2016
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.851 0.120 4 4633549 intron variant C/A snv 0.20 0.010 1.000 1 2014 2014