Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4140564
rs4140564
0.010 GeneticVariation BEFREE The top seven associations were subsequently tested in samples from the Netherlands (306 cases and 584 controls). rs4140564 on chromosome 1 mapping 5' to both the PTGS2 and PLA2G4A genes was associated with risk of knee OA in all the cohorts studied (overall odds ratio OR(mh) = 1.55 95% C.I.1.30-1.85, p < 6.9 x 10(-7)). 18471798

2008

dbSNP: rs4764133
rs4764133
0.010 GeneticVariation BEFREE The DNA variant near the MGP gene was validated in three additional studies, which resulted in a highly significant association between the MGP variant and hand OA (rs4764133, Beta<sub>meta</sub>=0.83, P<sub>meta</sub>=1.8*10<sup>-15</sup>). 28855172

2017

dbSNP: rs643472
rs643472
0.010 GeneticVariation BEFREE The current research genotyped four SNPs in 306 OA patients and 316 healthy controls, including PRNCR1 rs7463708, PRNCR1 rs1456315, PRNCR1 rs16901946 and KIF13B1 rs643472, to investigate their associations with OA susceptibility. 29714128

2018

dbSNP: rs6766414
rs6766414
0.010 GeneticVariation BEFREE In the comparison of hypertrophic with non-hypertrophic OA the most significant variant was located between <i>STT3B</i> and <i>GADL1</i> (rs6766414, p=3.13×10<sup>-6</sup>, OR (95% CIs) 1.45 (1.24 to 1.69)). 27974301

2017

dbSNP: rs9350591
rs9350591
0.010 GeneticVariation BEFREE Functional characterisation of the osteoarthritis susceptibility locus at chromosome 6q14.1 marked by the polymorphism rs9350591. 26346884

2015

dbSNP: rs4343
rs4343
ACE
0.010 GeneticVariation BEFREE Significant correlation exists between ACE rs4343 and rs4362 polymorphisms and OA. 26261641

2015

dbSNP: rs4362
rs4362
ACE
0.010 GeneticVariation BEFREE Significant correlation exists between ACE rs4343 and rs4362 polymorphisms and OA. 26261641

2015

dbSNP: rs1800682
rs1800682
0.010 GeneticVariation BEFREE Fas (rs1800682) and FasL (rs763110) polymorphism were associated with the risk of IVDD and Fas (rs2234767) was correlated to the susceptibility of OA and RA. 29734947

2018

dbSNP: rs2234767
rs2234767
0.010 GeneticVariation BEFREE Fas (rs1800682) and FasL (rs763110) polymorphism were associated with the risk of IVDD and Fas (rs2234767) was correlated to the susceptibility of OA and RA. 29734947

2018

dbSNP: rs1871054
rs1871054
0.040 GeneticVariation BEFREE In summary, we have identified that the rs1871054 variant within the ADAM12 gene is a risk factor for increased osteoarthritis susceptibility and severity. 25667922

2015

dbSNP: rs1871054
rs1871054
0.040 GeneticVariation BEFREE The rs1871054 polymorphism was not related to OA susceptibility or to progression traits. 19268722

2009

dbSNP: rs1871054
rs1871054
0.040 GeneticVariation BEFREE We found that the rs1871054 was significantly associated with the risk of knee OA (allele model OR 1.72, 95% CI 1.43-2.07, P < 0.001; additive model: OR 2.06, 95% CI 1.19-3.56, P = 0.010; dominant model: OR 2.45, 95% CI 1.85-3.25, P < 0.001; recessive model: OR 1.54, 95% CI 1.13-2.10, P = 0.007). rs1044122 was significantly associated with knee OA susceptibility in recessive model (OR 1.45, 95% CI 1.03-2.04, P = 0.031). 28748424

2017

dbSNP: rs1871054
rs1871054
0.040 GeneticVariation BEFREE In conclusion, our data demonstrated the ADAM12 rs1871054 variant was found to be significantly associated with increased OA susceptibility in a Chinese Han population. 25197389

2014

dbSNP: rs3740199
rs3740199
0.030 GeneticVariation BEFREE We conclude that rs3740199 polymorphism may affect occurrence of knee OA and its progression. 19268722

2009

dbSNP: rs3740199
rs3740199
0.030 GeneticVariation BEFREE In the stratified analysis by gender, significant association was identified with the risk of knee OA for rs3740199 in men in allele model (OR 2.41, 95% CI 1.51-3.84, P < 0.001), dominant model (OR 2.68, 95% CI 1.17-6.14, P = 0.02) and recessive model (OR 3.51, 95% CI 1.68-7.36, P = 0.001), but not for additive model (OR 1.30, 95% CI 0.81-2.08, P = 0.28). 28748424

2017

dbSNP: rs3740199
rs3740199
0.030 GeneticVariation BEFREE The rs3740199 in ADAM12 was associated with knee OA susceptibility in Thai male patients, and individuals with the CC genotype carried the highest risk when compared with the GG and GC genotypes. 26875044

2016

dbSNP: rs1044122
rs1044122
0.010 GeneticVariation BEFREE We found that the rs1871054 was significantly associated with the risk of knee OA (allele model OR 1.72, 95% CI 1.43-2.07, P < 0.001; additive model: OR 2.06, 95% CI 1.19-3.56, P = 0.010; dominant model: OR 2.45, 95% CI 1.85-3.25, P < 0.001; recessive model: OR 1.54, 95% CI 1.13-2.10, P = 0.007). rs1044122 was significantly associated with knee OA susceptibility in recessive model (OR 1.45, 95% CI 1.03-2.04, P = 0.031). 28748424

2017

dbSNP: rs1278279
rs1278279
0.010 GeneticVariation BEFREE For rs3740199 and rs1278279, no significant associations with knee OA were found. 28748424

2017

dbSNP: rs4747096
rs4747096
0.010 GeneticVariation BEFREE In conclusion, the nsSNP rs4747096 in ADAMTS14 was associated with knee OA in female Thai patients; therefore, the role of ADAMTS14 in OA seems to be gender-dependent. 24301791

2013

dbSNP: rs11807350
rs11807350
0.010 GeneticVariation BEFREE These findings suggest that the ADAMTS4 (rs4233367 and rs11807350) and ADAMTS5 (rs226794 and rs2830585) variants examined may not contribute to susceptibility to knee OA in the Turkish population. 27706574

2016

dbSNP: rs4233367
rs4233367
0.010 GeneticVariation BEFREE These findings suggest that the ADAMTS4 (rs4233367 and rs11807350) and ADAMTS5 (rs226794 and rs2830585) variants examined may not contribute to susceptibility to knee OA in the Turkish population. 27706574

2016

dbSNP: rs226794
rs226794
0.030 GeneticVariation BEFREE These findings suggest that the ADAMTS4 (rs4233367 and rs11807350) and ADAMTS5 (rs226794 and rs2830585) variants examined may not contribute to susceptibility to knee OA in the Turkish population. 27706574

2016

dbSNP: rs226794
rs226794
0.030 GeneticVariation BEFREE Initial analyses of 2 sample collections (n = 277 and n = 159) showed a trend toward decreased frequency of the putative deleterious allele of rs226794 among patients with severe knee OA (P = 0.047 versus controls). 18240210

2008

dbSNP: rs226794
rs226794
0.030 GeneticVariation BEFREE The rs2830585 polymorphism, but not rs226794 polymorphism, was significantly associated with an increased risk of knee OA. 30652828

2019

dbSNP: rs2830585
rs2830585
0.020 GeneticVariation BEFREE In conclusion, the ADAMTS5 rs2830585 polymorphism may be involved in the development of knee OA by destroying the extracellular matrix, but this finding should be further confirmed by larger studies. 30652828

2019