rs6479778, ARID5B

N. diseases: 5
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.
Acute lymphocytic leukemia
CUI: C0023449
Disease: Acute lymphocytic leukemia
222 0.827 0.200 10 61929318 intron variant T/C;G snv 0.010 1.000 1 2017 2017
Autoimmune thyroid disease (AITD)
CUI: C3840565
Disease: Autoimmune thyroid disease (AITD)
54 0.827 0.200 10 61929318 intron variant T/C;G snv 0.010 1.000 1 2013 2013
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.827 0.200 10 61929318 intron variant T/C;G snv 0.010 1.000 1 2013 2013
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
131 0.827 0.200 10 61929318 intron variant T/C;G snv 0.010 1.000 1 2013 2013
Precursor Cell Lymphoblastic Leukemia Lymphoma
CUI: C1961102
Disease: Precursor Cell Lymphoblastic Leukemia Lymphoma
168 0.827 0.200 10 61929318 intron variant T/C;G snv 0.010 1.000 1 2017 2017