Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7481311
rs7481311
0.010 GeneticVariation BEFREE Haplotype analysis shown that haplotype "GCC" in the block (rs988712, rs7481311, and rs11030064) increased LDH risk (OR = 1.49, 95% CI = 1.06-2.10, p = 0.022) at age ≤50 years. 30143695

2018

dbSNP: rs79845319
rs79845319
0.010 GeneticVariation BEFREE The SNP rs17576 was found to be significantly associated with susceptibility to LDH (OR = 0.77, p = 0.0002), which was also confirmed by haplotype-based analyses (rs79845319-rs17576-rs45437897, global p < 0.001). 30289281

2018

dbSNP: rs886205
rs886205
0.010 GeneticVariation BEFREE Additionally, the haplotype "GGCTCACG" constructed by rs886205, rs2238152, rs4648328, rs441, rs4646778, rs671, rs11066028, and rs7296651 was associated with increased risk of LDH (OR = 1.45; 95% CI = 1.11-1.90; P = 0.0071). 30166580

2018

dbSNP: rs143383
rs143383
0.010 GeneticVariation BEFREE The aim of the present study is to assess whether the single nucleotide polymorphism in the GDF5 (+104T/C; rs143383) is associated with the symptomatic lumbar disc herniation in the Chinese Han population and the identification of the mechanisms of its action. 24105021

2014

dbSNP: rs2615977
rs2615977
0.010 GeneticVariation BEFREE This corresponded with observations in LDH but the SNP was not associated with OA.We did not observe AEI at rs2615977. 23497244

2013

dbSNP: rs1799971
rs1799971
0.010 GeneticVariation BEFREE Pain intensity the first year after lumbar disc herniation is associated with the A118G polymorphism in the opioid receptor mu 1 gene: evidence of a sex and genotype interaction. 22815498

2012

dbSNP: rs4680
rs4680
0.010 GeneticVariation BEFREE We conclude that the functional COMT Val158Met SNP contributes to long lasting low back pain, sciatica and disability after lumbar disc herniation. 22337560

2012

dbSNP: rs1400328611
rs1400328611
TNF
0.010 GeneticVariation BEFREE The eNOS (-786 T/C) and iNOS (22 G/A) SNPs were more frequent among the control subjects, suggesting their possible protective role against LDH. 21837414

2011

dbSNP: rs375081888
rs375081888
0.010 GeneticVariation BEFREE The eNOS (-786 T/C) and iNOS (22 G/A) SNPs were more frequent among the control subjects, suggesting their possible protective role against LDH. 21837414

2011

dbSNP: rs762704392
rs762704392
0.010 GeneticVariation BEFREE The eNOS (-786 T/C) and iNOS (22 G/A) SNPs were more frequent among the control subjects, suggesting their possible protective role against LDH. 21837414

2011

dbSNP: rs9406328
rs9406328
0.010 GeneticVariation BEFREE An intronic SNP in THBS2 (IVS10-8C --> T; rs9406328) showed significant association (p = 0.0000028) with LDH in two independent Japanese populations. 18455130

2008