rs11086102, None

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.
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
142 0.882 19 18287818 upstream gene variant G/C snv 0.64 0.700 1.000 1 2019 2019
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
132 0.882 19 18287818 upstream gene variant G/C snv 0.64 0.700 1.000 1 2019 2019
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
141 0.882 19 18287818 upstream gene variant G/C snv 0.64 0.700 1.000 1 2019 2019
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.882 19 18287818 upstream gene variant G/C snv 0.64 0.700 1.000 1 2019 2019
Monocyte count procedure
CUI: C0200637
Disease: Monocyte count procedure
296 0.882 19 18287818 upstream gene variant G/C snv 0.64 0.700 1.000 1 2016 2016
Monocyte count result
CUI: C0750880
Disease: Monocyte count result
296 0.882 19 18287818 upstream gene variant G/C snv 0.64 0.700 1.000 1 2016 2016