rs71508903, ARID5B

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.
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.807 0.160 10 62020112 intron variant C/T snv 0.15 0.800 1.000 2 2014 2019
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
142 0.807 0.160 10 62020112 intron variant C/T snv 0.15 0.700 1.000 1 2019 2019
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
132 0.807 0.160 10 62020112 intron variant C/T snv 0.15 0.700 1.000 1 2019 2019
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
141 0.807 0.160 10 62020112 intron variant C/T snv 0.15 0.700 1.000 1 2019 2019
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.807 0.160 10 62020112 intron variant C/T snv 0.15 0.700 1.000 1 2019 2019
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
283 0.807 0.160 10 62020112 intron variant C/T snv 0.15 0.700 1.000 1 2019 2019
Vitiligo
CUI: C0042900
Disease: Vitiligo
249 0.807 0.160 10 62020112 intron variant C/T snv 0.15 0.700 1.000 1 2016 2016