rs5050, AGT

N. diseases: 7
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.
Astrocytoma
CUI: C0004114
Disease: Astrocytoma
59 0.827 0.200 1 230714140 intron variant T/C;G snv 0.010 1.000 1 2018 2018
AURAL ATRESIA, CONGENITAL
CUI: C1842937
Disease: AURAL ATRESIA, CONGENITAL
29 0.827 0.200 1 230714140 intron variant T/C;G snv 0.010 1.000 1 2019 2019
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.827 0.200 1 230714140 intron variant T/C;G snv 0.010 1.000 1 2019 2019
Childhood Astrocytoma
CUI: C4086152
Disease: Childhood Astrocytoma
39 0.827 0.200 1 230714140 intron variant T/C;G snv 0.010 1.000 1 2018 2018
Coronary Aneurysm
CUI: C0010051
Disease: Coronary Aneurysm
17 0.827 0.200 1 230714140 intron variant T/C;G snv 0.010 1.000 1 2019 2019
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.827 0.200 1 230714140 intron variant T/C;G snv 0.010 1.000 1 2014 2014
Mucocutaneous Lymph Node Syndrome
CUI: C0026691
Disease: Mucocutaneous Lymph Node Syndrome
195 0.827 0.200 1 230714140 intron variant T/C;G snv 0.010 1.000 1 2019 2019