rs3918186, NOS3

N. diseases: 2
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.
Childhood Acute Lymphoblastic Leukemia
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
261 1.000 0.120 7 151005344 intron variant A/T snv 0.12 0.010 1.000 1 2013 2013
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 1.000 0.120 7 151005344 intron variant A/T snv 0.12 0.010 1.000 1 2015 2015