Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1799969
rs1799969
CUI: C0014175
Disease: Endometriosis
Endometriosis
0.040 GeneticVariation BEFREE This study suggests that polymorphisms K469E, G241R, and G634C are not associated with increased susceptibility to endometriosis in Brazilian women. 27614631

2016

dbSNP: rs1799969
rs1799969
CUI: C0014175
Disease: Endometriosis
Endometriosis
0.040 GeneticVariation BEFREE Reported associations of the G241R and K469E polymorphisms of the intercellular adhesion molecule-1 gene (ICAM-1) gene with endometriosis have differed in magnitude. 25859827

2015

dbSNP: rs1799969
rs1799969
CUI: C0014175
Disease: Endometriosis
Endometriosis
0.040 GeneticVariation BEFREE The K469E and G241R polymorphisms in the ICAM-1 gene and the C-634G polymorphism in the IL-6 gene may not be genetic factors related to susceptibility to advanced-stage endometriosis in the Korean population. 20160446

2010

dbSNP: rs1799969
rs1799969
CUI: C0014175
Disease: Endometriosis
Endometriosis
0.040 GeneticVariation BEFREE While the functional correlate of the G/R241 polymorphism remains unclear, this finding indicates that a genetic polymorphism in the ICAM-1 gene domain may contribute to the susceptibility to endometriosis. 12529420

2003

dbSNP: rs1799969
rs1799969
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.030 GeneticVariation BEFREE In addition, the meta-analysis revealed a significant association between the ICAM-1 G241R R allele and Behcet's disease</span> (B</span>D) (OR = 3.261, 95% CI = 1.653-6.434, p = 0.001), but not giant cell arteritis. 27894415

2016

dbSNP: rs1799969
rs1799969
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.030 GeneticVariation BEFREE Moreover, the meta-analysis indicated an association between RA and the R allele and RR+ RG genotype of the ICAM-1 G241R</span> polymorphism (OR = 2.014, 95% CI = 1.215-3.339, p = 0.007; OR = 2.394, 95% CI = 1.354-4.235, p = 0.003). 27894415

2016

dbSNP: rs1799969
rs1799969
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.030 GeneticVariation BEFREE Behçet's disease was associated with the ICAM1 E469, genotype ICAM1 469 E/E, ICAM1 241 G/R polymorphisms in different ethnic groups. 24645721

2014

dbSNP: rs1799969
rs1799969
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.030 GeneticVariation BEFREE To investigate the association of sICAM-1 and sVCAM-1 with ICAM1 721G>A and VCAM1 1238G>C polymorphisms and rheumatoid arthritis (RA) clinical activity, sixty RA patients and 60 healthy non-related subjects (HS) matched for age and sex were recruited. 19597294

2009

dbSNP: rs1799969
rs1799969
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.030 GeneticVariation BEFREE Our preliminary findings show that G/R 241 polymorphism of ICAM-1 is associated with RA, and that this confers a reduced risk of extra-articular manifestations and is associated with a slow rate of joint destruction. 11072593

2001

dbSNP: rs1799969
rs1799969
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.030 GeneticVariation BEFREE Our findings show that G/R 241 polymorphism of ICAM-1 is associated with BD susceptibility. 11409120

2001

dbSNP: rs1799969
rs1799969
CUI: C0018378
Disease: Guillain-Barre Syndrome
Guillain-Barre Syndrome
0.020 GeneticVariation BEFREE We found a significant protective association between heterozygous GA genotype in ICAM1 (241Gly/Arg) and GBS (p < .047). 31464097

2019

dbSNP: rs1799969
rs1799969
CUI: C0018378
Disease: Guillain-Barre Syndrome
Guillain-Barre Syndrome
0.020 GeneticVariation BEFREE IL-17 (Glu126Gly) mutant and ICAM-1 (Gly241Arg) heterozygous genotypes were strongly associated with increased risk of GBS (p < 0.016; OR = 3.706, 95% CI = 1.28-10.67; p < 0.001; OR = 4.148, 95% CI = 2.119-8.119, respectively). 27595159

2017

dbSNP: rs1799969
rs1799969
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
0.020 GeneticVariation BEFREE Although Gly241Arg polymorphism have not shown significant association with PCOS. 27039809

2016

dbSNP: rs1799969
rs1799969
CUI: C0039483
Disease: Giant Cell Arteritis
Giant Cell Arteritis
0.020 GeneticVariation BEFREE In addition, the meta-analysis revealed a significant association between the ICAM-1 G241R R allele and Behcet's disease (BD) (OR = 3.261, 95% CI = 1.653-6.434, p = 0.001), but not giant cell arteritis. 27894415

2016

dbSNP: rs1799969
rs1799969
CUI: C0018213
Disease: Graves Disease
Graves Disease
0.020 GeneticVariation BEFREE Although there is not association between ICAM1 (G241R and K469E), VCAM1 (T-1591C and T-833C), and E-selectin (S128R) SNPs and susceptibility to GD, higher anti-TPO in E-selectin 128 SR + RR, and lower TSH in ICAM1 469 KE + EE subjects suspect that these genotypes are prone to increased antithyroid autoantibody production with more accentuated TSH suppression in GD. 23242661

2013

dbSNP: rs1799969
rs1799969
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
0.020 GeneticVariation BEFREE This study examined the possible association of G241R and K469E single nucleotide polymorphisms (SNPs) of ICAM-1 gene with the occurrence and clinical/biochemical characteristics of polycystic ovary syndrome (PCOS). 21717173

2011

dbSNP: rs1799969
rs1799969
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.020 GeneticVariation BEFREE The findings indicate that polymorphisms of G241R are rare in Chinese population and that KK genotype of ICAM-1 K469E is significantly associated with well differentiation of CRC. 19822019

2009

dbSNP: rs1799969
rs1799969
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.020 GeneticVariation BEFREE Therefore, in our population our results discard the important previously described role of ICAM1 G241R in celiac disease. 18703101

2008

dbSNP: rs1799969
rs1799969
CUI: C0018213
Disease: Graves Disease
Graves Disease
0.020 GeneticVariation BEFREE We found no association of G241R and K469E polymorphisms of the ICAM-1gene with the development of GD in a Chinese population. 17873320

2007

dbSNP: rs1799969
rs1799969
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.020 GeneticVariation BEFREE The aim of this study was to investigate polymorphisms in the NOD2/CARD15 (R702W, G908R, and 3020insC), NOD1/CARD4 (E266K, D372N), and ICAM-1 (G241R, K469E) genes, which are known to be associated with inflammation, in Turkish patients with inflammatory bowel disease and healthy control groups. 16741608

2006

dbSNP: rs1799969
rs1799969
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.020 GeneticVariation BEFREE No significant differences were observed in the F206L polymorphism of L-selectin, or the G241R and E469K polymorphisms in the ICAM-1 gene in CD. 16916660

2006

dbSNP: rs1799969
rs1799969
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.020 GeneticVariation BEFREE In the second approach, we typed four nonsynonymous polymorphisms in genes C3 (R102G and L314P) and ICAM1 (G241R and K469E) in four independent cohorts totaling 2178 IBD cases. 16570073

2006

dbSNP: rs1799969
rs1799969
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.020 GeneticVariation BEFREE We studied the association of SNPs in the IL-6 (-174G>C), IL-8 (-251T>A), TNFalpha (-308G>A), ICAM-1 (R241G and K469E), and PPARgamma (Pro12Ala) genes and the risk of CRC. 16937502

2006

dbSNP: rs1799969
rs1799969
CUI: C0039483
Disease: Giant Cell Arteritis
Giant Cell Arteritis
0.020 GeneticVariation BEFREE Our findings show that G/R 241 polymorphism of ICAM-1 is associated with PMR/GCA susceptibility and confers an increased risk of relapse/recurrence in PMR. 10813290

2000

dbSNP: rs1799969
rs1799969
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 GeneticVariation BEFREE Genomic DNA was isolated from whole blood for the analysis of <i>VEGF-A</i> (rs2010963, 1570360, rs699947), <i>ICAM-1</i> (rs5498, rs1799969) SNPs and from tumor tissue for the detection of genomic variants in <i>KRAS</i>, <i>NRAS</i>, <i>BRAF</i> genes. 31752122

2019