CALR, calreticulin, 811

N. diseases: 487; N. variants: 9
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2974751
rs2974751
Entrez Id: 811
Gene Symbol: CALR
CALR
CUI: C0017654
Disease:
Glomerular Filtration Rate
A 0.700 GeneticVariation GWASCAT A catalog of genetic loci associated with kidney function from analyses of a million individuals. 31152163 2019
dbSNP: rs1010222
rs1010222
Entrez Id: 811
Gene Symbol: CALR
CALR
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean
0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs1010222
rs1010222
Entrez Id: 811
Gene Symbol: CALR
CALR
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin
0.700 GeneticVariation GWASDB Genetic Loci implicated in erythroid differentiation and cell cycle regulation are associated with red blood cell traits. 22560525 2012
dbSNP: rs1049481
rs1049481
Entrez Id: 811;5886
Gene Symbol: CALR;RAD23A
CALR;RAD23A
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean
0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs1010222
rs1010222
Entrez Id: 811
Gene Symbol: CALR
CALR
CUI: C0014772
Disease:
Red Blood Cell Count measurement
0.700 GeneticVariation GWASDB Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. 19862010 2009
dbSNP: rs1555760738
rs1555760738
Entrez Id: 811
Gene Symbol: CALR
CALR
CUI: C3277671
Disease:
THROMBOCYTHEMIA 1
A 0.700 CausalMutation CLINVAR
dbSNP: rs1555760738
rs1555760738
Entrez Id: 811
Gene Symbol: CALR
CALR
CUI: C0001815
Disease:
Primary Myelofibrosis
A 0.700 CausalMutation CLINVAR
dbSNP: rs1378379005
rs1378379005
Entrez Id: 811;102466659
Gene Symbol: CALR;MIR6515
CALR;MIR6515
CUI: C0027022
Disease:
Myeloproliferative disease
0.010 GeneticVariation BEFREE To analyze the relationship between six polymorphisms in genes related to oxidative stress, namely CAT-262 C>T, MnSOD Ala16Val, GPX1 Pro198Leu, GSTM1 and GSTT1 null genotypes, and GSTP1 Ile105Val, and the occurrence of BCR-ABL negative myeloproliferative neoplasms (polycythemia vera, essential thrombocythemia, and primary myelofibrosis). 27077777 2016
dbSNP: rs147368353
rs147368353
Entrez Id: 811;102466659
Gene Symbol: CALR;MIR6515
CALR;MIR6515
CUI: C0027022
Disease:
Myeloproliferative disease
0.010 GeneticVariation BEFREE To analyze the relationship between six polymorphisms in genes related to oxidative stress, namely CAT-262 C>T, MnSOD Ala16Val, GPX1 Pro198Leu, GSTM1 and GSTT1 null genotypes, and GSTP1 Ile105Val, and the occurrence of BCR-ABL negative myeloproliferative neoplasms (polycythemia vera, essential thrombocythemia, and primary myelofibrosis). 27077777 2016
dbSNP: rs149740908
rs149740908
Entrez Id: 811;102466659
Gene Symbol: CALR;MIR6515
CALR;MIR6515
CUI: C0036337
Disease:
Schizoaffective Disorder
0.010 GeneticVariation BEFREE Following screening of the gene in 60 independent cases of schizoaffective disorder, we report novel germ-line mutations at positions -205 C > T and the conserved exon 5 (c: 682 C > T, pro228ser) in two unrelated cases of schizoaffective disorder. 19760677 2010
dbSNP: rs777628969
rs777628969
Entrez Id: 811;102466659
Gene Symbol: CALR;MIR6515
CALR;MIR6515
CUI: C0027794
Disease:
Neural Tube Defects
0.010 GeneticVariation BEFREE Loop-tail (Lp) mice show a very severe neural tube defect (craniorachischisis) caused by mutations in the Vangl2 gene (D255E, S464N). 20329788 2010
dbSNP: rs149740908
rs149740908
Entrez Id: 811;102466659
Gene Symbol: CALR;MIR6515
CALR;MIR6515
CUI: C0010495
Disease:
Cutis Laxa
0.010 GeneticVariation BEFREE Histological analysis of skin sections from a cutis laxa patient with a homozygous S227P mutation showed a lack of fibulin-5 in the extracellular matrix and a concomitant disorganization of dermal elastic fibers. 17035250 2006
dbSNP: rs756312947
rs756312947
Entrez Id: 811;102466659
Gene Symbol: CALR;MIR6515
CALR;MIR6515
CUI: C0032227
Disease:
Pleural effusion disorder
0.010 GeneticVariation BEFREE Additionally, SLE patients with Thr/Thr187 and Ile/Thr187 genotypes were more likely to have pleural effusions (P = 0.038, OR 1.874 [95% CI 1.033-3.411]) and anti-SSA/Ro antibody production (P = 0.046, OR 2.221 [95% CI 1.013-4.897]). 17133600 2006
dbSNP: rs756312947
rs756312947
Entrez Id: 811;102466659
Gene Symbol: CALR;MIR6515
CALR;MIR6515
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic
0.010 GeneticVariation BEFREE To investigate the possible association of the Fcgamma receptor IIb (FcgammaRIIb) Ile/Thr187 transmembrane domain polymorphism, which significantly affects receptor signaling, with susceptibility to systemic lupus erythematosus (SLE) in Taiwanese patients. 17133600 2006