Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1801157
rs1801157
CUI: C0019693
Disease: HIV Infections
HIV Infections
0.010 GeneticVariation BEFREE After adjusting by age, route of HIV infection, length of infection before cART and viral hepatitis coinfection, CCR2 rs1799864-AG genotype was significantly associated with INR status (OR [95% CI]: 1.80 [1.04-3.11]; p = 0.04), and CXCL12 rs1801157-TT genotype showed a trend (OR [95% CI]: 2.47 [0.96-6.35]; p = 0.06). 30921390

2019

dbSNP: rs1801157
rs1801157
CUI: C0275524
Disease: Coinfection
Coinfection
0.010 GeneticVariation BEFREE After adjusting by age, route of HIV infection, length of infection before cART and viral hepatitis coinfection, CCR2 rs1799864-AG genotype was significantly associated with INR status (OR [95% CI]: 1.80 [1.04-3.11]; p = 0.04), and CXCL12 rs1801157-TT genotype showed a trend (OR [95% CI]: 2.47 [0.96-6.35]; p = 0.06). 30921390

2019

dbSNP: rs1801157
rs1801157
CUI: C0343641
Disease: Human papilloma virus infection
Human papilloma virus infection
0.010 GeneticVariation BEFREE In the present study, we demonstrated that CXCL12 rs1801157 is independently associated with HPV infection and exerts influence in HSIL development, suggesting it as a promising susceptibility biomarker for HPV infection and lesions development. 30227860

2018

dbSNP: rs1801157
rs1801157
Diabetes Mellitus, Non-Insulin-Dependent
0.010 GeneticVariation BEFREE Conclusion Both dominant and additive models in both KCNJ11 (E23K, rs5219) and SDF-1β (G801A, rs1801157) genetic polymorphisms are significantly associated with type 2 diabetes. 29893194

2018

dbSNP: rs1801157
rs1801157
CUI: C3539878
Disease: Triple Negative Breast Neoplasms
Triple Negative Breast Neoplasms
0.010 GeneticVariation BEFREE The present study analyzed genetic polymorphisms in CXCL12 (rs1801157, G > A) and CXCR4 (rs2228014, C > T) and CXCR4 immunostaining in tumor tissues from patients with triple negative breast cancer (TNBC) aiming to evaluate their possible role in its' susceptibility and prognosis. 29926386

2018

dbSNP: rs1801157
rs1801157
CUI: C4722518
Disease: Triple-Negative Breast Carcinoma
Triple-Negative Breast Carcinoma
0.010 GeneticVariation BEFREE The present study analyzed genetic polymorphisms in CXCL12 (rs1801157, G > A) and CXCR4 (rs2228014, C > T) and CXCR4 immunostaining in tumor tissues from patients with triple negative breast cancer (TNBC) aiming to evaluate their possible role in its' susceptibility and prognosis. 29926386

2018

dbSNP: rs1801157
rs1801157
CUI: C1456868
Disease: Diabetic foot ulcer
Diabetic foot ulcer
0.010 GeneticVariation BEFREE The Interleukin (IL)-6 (-174G > C/rs1800795), Tumor Necrosis Factor (TNF)-α (-308G > A/rs1800629) and (-238G > A/rs361525) and Stromal cell Derived Factor (SDF)-1 (+801G > A/rs1801157) are well characterized single nucleotide polymorphisms (SNPs) which were previously shown to be associated with Diabetic Foot Ulcer (DFU). 30009916

2018

dbSNP: rs1801157
rs1801157
CUI: C0376545
Disease: Hematologic Neoplasms
Hematologic Neoplasms
0.010 GeneticVariation BEFREE Several recent studies have shown that <i>SDF1</i>-3'A polymorphism (rs1801157) is associated with susceptibility to hematological malignancy, but published studies' results are disputed. 28352190

2017

dbSNP: rs1801157
rs1801157
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.010 GeneticVariation BEFREE <i>SDF-1</i> rs1801157 polymorphism may not influence the risk of SLE. 29088886

2017

dbSNP: rs1801157
rs1801157
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.010 GeneticVariation BEFREE In summary, this study suggested that the SDF-1 rs1801157 polymorphism may serve as a risk factor for cancer development among Asians, especially an increased risk of urologic and lung cancers. 27265091

2016

dbSNP: rs1801157
rs1801157
CUI: C1332977
Disease: Childhood Leukemia
Childhood Leukemia
0.010 GeneticVariation BEFREE This study aimed to determine the associations between the polymorphisms located on the SDF-1 (rs1801157, G>A) and CXCR4 (rs2228014, C>T) encoding genes and susceptibility and leukemia cell dissemination in AML. 27154815

2016

dbSNP: rs1801157
rs1801157
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia
0.010 GeneticVariation BEFREE In conclusion, data from this study indicate that the CXCL12 rs1801157 G > A polymorphism may affect CLL development, disease progression as well as response to treatment. 27173875

2016

dbSNP: rs1801157
rs1801157
CUI: C0751571
Disease: Cancer of Urinary Tract
Cancer of Urinary Tract
0.010 GeneticVariation BEFREE Moreover, we confirmed that the SDF-1 rs1801157 gene polymorphism was only associated with lung and urologic cancer risk. 27265091

2016

dbSNP: rs1801157
rs1801157
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.010 GeneticVariation BEFREE Genotype CT of rs2228014 appeared to correlate with AML risk, but played no role in leukemia cells invading the bloodstream, while rs1801157 and the two combined SNPs were not associated with either increased AML risk or extramedullary leukemia-cell dissemination. 27154815

2016

dbSNP: rs1801157
rs1801157
CUI: C0023418
Disease: leukemia
leukemia
0.010 GeneticVariation BEFREE This study aimed to determine the associations between the polymorphisms located on the SDF-1 (rs1801157, G>A) and CXCR4 (rs2228014, C>T) encoding genes and susceptibility and leukemia cell dissemination in AML. 27154815

2016

dbSNP: rs1801157
rs1801157
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.010 GeneticVariation BEFREE Lack of an Association between the SDF-1 rs1801157 Polymorphism and Coronary Heart Disease: A Meta-Analysis. 26133117

2015

dbSNP: rs1801157
rs1801157
CUI: C0342257
Disease: Complications of Diabetes Mellitus
Complications of Diabetes Mellitus
0.010 GeneticVariation BEFREE The IL-6 -174G/C (rs1800795), TNF-α -308G/A (rs1800629) and -238G/A (rs361525) and SDF-1 801G/A (rs1801157) are well characterized SNPs which have previously been linked to various diabetic complications. 25839939

2015

dbSNP: rs1801157
rs1801157
Childhood Acute Lymphoblastic Leukemia
0.010 GeneticVariation BEFREE Genetic polymorphisms in the 3'UTR region of the CXCL12 (rs1801157) and TP53 codon 72 (rs1042522) genes may contribute to susceptibility to childhood ALL because they affect some important processes, such as metastasis regulation and tumor suppression. 23653000

2013

dbSNP: rs1801157
rs1801157
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia
0.010 GeneticVariation BEFREE Genetic polymorphisms in the 3'UTR region of the CXCL12 (rs1801157) and TP53 codon 72 (rs1042522) genes may contribute to susceptibility to childhood ALL because they affect some important processes, such as metastasis regulation and tumor suppression. 23653000

2013

dbSNP: rs1801157
rs1801157
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
Adult Acute Lymphocytic Leukemia
0.010 GeneticVariation BEFREE Genetic polymorphisms in the 3'UTR region of the CXCL12 (rs1801157) and TP53 codon 72 (rs1042522) genes may contribute to susceptibility to childhood ALL because they affect some important processes, such as metastasis regulation and tumor suppression. 23653000

2013

dbSNP: rs1801157
rs1801157
Infections specific to perinatal period
0.010 GeneticVariation BEFREE Our results indicate that the rs1801157 SNP does not influence perinatal infection, but impacts disease progression. 22962615

2012

dbSNP: rs1801157
rs1801157
CUI: C0085215
Disease: Ovarian Failure, Premature
Ovarian Failure, Premature
0.010 GeneticVariation BEFREE The A allele of CXCL12 polymorphism rs1801157 is a possible risk factor for developing POF. 21296802

2011

dbSNP: rs1801157
rs1801157
CUI: C1862382
Disease: SVEINSSON CHORIORETINAL ATROPHY
SVEINSSON CHORIORETINAL ATROPHY
0.010 GeneticVariation BEFREE Expression of the CXCL12 (SNP rs1801157) polymorphisms GA/AA significantly correlated with distant metastasis (P=0.026), but not with prognosis. 21584490

2011

dbSNP: rs1801157
rs1801157
CUI: C0025322
Disease: Premature Menopause
Premature Menopause
0.010 GeneticVariation BEFREE The A allele of CXCL12 polymorphism rs1801157 is a possible risk factor for developing POF. 21296802

2011

dbSNP: rs1801157
rs1801157
CUI: C0220644
Disease: Childhood Hodgkin Lymphoma
Childhood Hodgkin Lymphoma
0.010 GeneticVariation BEFREE The single-nucleotide polymorphism (SNP) rs1801157 (previously known as CXCL12-A/ stromal cell-derived factor-1 (SDF1)-3'A) in CXCL12/SDF1 gene was assessed in breast cancer, Hodgkin's lymphoma (HL), and non-Hodgkin's lymphoma (NHL), since the chemokine CXCL12, previously known as SDF1, and its receptor CXCR4 regulate leukocyte trafficking and many essential biological processes, including tumor growth, angiogenesis, and metastasis of different types of tumors. 19927352

2009