rs2456449, CASC19;PCAT1

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.
Chronic Lymphocytic Leukemia
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
291 0.827 0.280 8 127180736 intron variant A/G snv 0.30 0.720 1.000 2 2010 2010
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.827 0.280 8 127180736 intron variant A/G snv 0.30 0.700 1.000 1 2013 2013
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.827 0.280 8 127180736 intron variant A/G snv 0.30 0.700 1.000 1 2010 2010
Monoclonal B-Cell Lymphocytosis
CUI: C2698259
Disease: Monoclonal B-Cell Lymphocytosis
7 0.827 0.280 8 127180736 intron variant A/G snv 0.30 0.010 1.000 1 2010 2010
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.827 0.280 8 127180736 intron variant A/G snv 0.30 0.010 1.000 1 2012 2012