Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894649
rs104894649
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B
CUI: C3150354
Disease:
IMMUNODEFICIENCY, COMMON VARIABLE, 2
T 0.800 CausalMutation CLINVAR
dbSNP: rs34557412
rs34557412
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B
CUI: C3150354
Disease:
IMMUNODEFICIENCY, COMMON VARIABLE, 2
G 0.800 SusceptibilityMutation CLINVAR
dbSNP: rs34557412
rs34557412
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B
CUI: C3150354
Disease:
IMMUNODEFICIENCY, COMMON VARIABLE, 2
G 0.800 CausalMutation CLINVAR
dbSNP: rs34557412
rs34557412
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B
CUI: C1836032
Disease:
Immunoglobulin a deficiency 2
G 0.800 CausalMutation CLINVAR
dbSNP: rs104894650
rs104894650
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B
CUI: C3150354
Disease:
IMMUNODEFICIENCY, COMMON VARIABLE, 2
T 0.700 CausalMutation CLINVAR
dbSNP: rs104894650
rs104894650
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B
CUI: C3150354
Disease:
IMMUNODEFICIENCY, COMMON VARIABLE, 2
C 0.700 CausalMutation CLINVAR
dbSNP: rs121908379
rs121908379
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B
CUI: C3150354
Disease:
IMMUNODEFICIENCY, COMMON VARIABLE, 2
TT 0.700 CausalMutation CLINVAR
dbSNP: rs1555550717
rs1555550717
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B
CUI: C3150354
Disease:
IMMUNODEFICIENCY, COMMON VARIABLE, 2
T 0.700 CausalMutation CLINVAR
dbSNP: rs72553875
rs72553875
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B
CUI: C3150354
Disease:
IMMUNODEFICIENCY, COMMON VARIABLE, 2
GT 0.700 GeneticVariation CLINVAR
dbSNP: rs72553883
rs72553883
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B
CUI: C1836032
Disease:
Immunoglobulin a deficiency 2
T 0.700 CausalMutation CLINVAR
dbSNP: rs72553883
rs72553883
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B
CUI: C3150354
Disease:
IMMUNODEFICIENCY, COMMON VARIABLE, 2
T 0.700 CausalMutation CLINVAR
dbSNP: rs4985726
rs4985726
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B
CUI: C1868683
Disease:
B-CELL MALIGNANCY, LOW-GRADE
0.010 GeneticVariation BEFREE Although the obtained P-values for all 20 SNPs did not reach statistical significance for this study (α = 0.003), the high value of the global chi-squared statistic (χ(2) df = 38  = 52.65; P = 0.0586), and obtained values of odds ratio indicate that rs9514828 (BAFF), rs3803800 (APRIL) and rs4985726 (TACI) may be associated with the risk of B-CLL. 26268376 2015
dbSNP: rs4985726
rs4985726
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B
CUI: C0023434
Disease:
Chronic Lymphocytic Leukemia
0.010 GeneticVariation BEFREE Although the obtained P-values for all 20 SNPs did not reach statistical significance for this study (α = 0.003), the high value of the global chi-squared statistic (χ(2) df = 38  = 52.65; P = 0.0586), and obtained values of odds ratio indicate that rs9514828 (BAFF), rs3803800 (APRIL) and rs4985726 (TACI) may be associated with the risk of B-CLL. 26268376 2015
dbSNP: rs11654088
rs11654088
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Association of common variants in TNFRSF13B, TNFSF13, and ANXA3 with serum levels of non-albumin protein and immunoglobulin isotypes in Japanese. 22558069 2012
dbSNP: rs2274892
rs2274892
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Association of common variants in TNFRSF13B, TNFSF13, and ANXA3 with serum levels of non-albumin protein and immunoglobulin isotypes in Japanese. 22558069 2012
dbSNP: rs3751991
rs3751991
Entrez Id: 23495;96597
Gene Symbol: TNFRSF13B;TBC1D27P
TNFRSF13B;TBC1D27P
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Association of common variants in TNFRSF13B, TNFSF13, and ANXA3 with serum levels of non-albumin protein and immunoglobulin isotypes in Japanese. 22558069 2012
dbSNP: rs3818716
rs3818716
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Association of common variants in TNFRSF13B, TNFSF13, and ANXA3 with serum levels of non-albumin protein and immunoglobulin isotypes in Japanese. 22558069 2012
dbSNP: rs4273077
rs4273077
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Association of common variants in TNFRSF13B, TNFSF13, and ANXA3 with serum levels of non-albumin protein and immunoglobulin isotypes in Japanese. 22558069 2012
dbSNP: rs4561508
rs4561508
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Association of common variants in TNFRSF13B, TNFSF13, and ANXA3 with serum levels of non-albumin protein and immunoglobulin isotypes in Japanese. 22558069 2012
dbSNP: rs4792800
rs4792800
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Association of common variants in TNFRSF13B, TNFSF13, and ANXA3 with serum levels of non-albumin protein and immunoglobulin isotypes in Japanese. 22558069 2012
dbSNP: rs4985700
rs4985700
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Association of common variants in TNFRSF13B, TNFSF13, and ANXA3 with serum levels of non-albumin protein and immunoglobulin isotypes in Japanese. 22558069 2012
dbSNP: rs4985726
rs4985726
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B
CUI: C0202202
Disease:
Protein measurement
G 0.700 GeneticVariation GWASCAT Association of common variants in TNFRSF13B, TNFSF13, and ANXA3 with serum levels of non-albumin protein and immunoglobulin isotypes in Japanese. 22558069 2012
dbSNP: rs4985726
rs4985726
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B
CUI: C0523465
Disease:
Serum albumin measurement
G 0.700 GeneticVariation GWASDB Association of common variants in TNFRSF13B, TNFSF13, and ANXA3 with serum levels of non-albumin protein and immunoglobulin isotypes in Japanese. 22558069 2012
dbSNP: rs7226097
rs7226097
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B
CUI: C0523465
Disease:
Serum albumin measurement
0.700 GeneticVariation GWASDB Association of common variants in TNFRSF13B, TNFSF13, and ANXA3 with serum levels of non-albumin protein and immunoglobulin isotypes in Japanese. 22558069 2012
dbSNP: rs34557412
rs34557412
Entrez Id: 23495
Gene Symbol: TNFRSF13B
TNFRSF13B
CUI: C2936664
Disease:
Acquired Hypogammaglobulinemia
0.040 GeneticVariation BEFREE B cells from patients with common variable immunodeficiency (CVID) who are heterozygous for transmembrane activator and CAML interactor (TACI) mutation C104R, which abolishes ligand binding, fail to produce Igs in response to TACI ligand. 17492055 2007