rs4985726, TNFRSF13B

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.
Blood Protein Measurement
CUI: C2985280
Disease: Blood Protein Measurement
2575 0.925 0.120 17 16960324 intron variant C/G snv 0.11 0.700 1.000 1 2018 2018
Protein measurement
CUI: C0202202
Disease: Protein measurement
422 0.925 0.120 17 16960324 intron variant C/G snv 0.11 0.700 1.000 1 2012 2012
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 0.925 0.120 17 16960324 intron variant C/G snv 0.11 0.700 1.000 1 2012 2012
B-CELL MALIGNANCY, LOW-GRADE
CUI: C1868683
Disease: B-CELL MALIGNANCY, LOW-GRADE
19 0.925 0.120 17 16960324 intron variant C/G snv 0.11 0.010 1.000 1 2015 2015
Chronic Lymphocytic Leukemia
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
291 0.925 0.120 17 16960324 intron variant C/G snv 0.11 0.010 1.000 1 2015 2015