rs4273077, TNFRSF13B

N. diseases: 4
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.
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.925 0.160 17 16945825 intron variant A/G snv 0.13 0.810 1.000 2 2013 2014
Protein measurement
CUI: C0202202
Disease: Protein measurement
422 0.925 0.160 17 16945825 intron variant A/G snv 0.13 0.700 1.000 1 2010 2010
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.925 0.160 17 16945825 intron variant A/G snv 0.13 0.700 1.000 1 2012 2012
Monoclonal Gammopathy of Undetermined Significance
CUI: C0026470
Disease: Monoclonal Gammopathy of Undetermined Significance
20 0.925 0.160 17 16945825 intron variant A/G snv 0.13 0.010 1.000 1 2014 2014