Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs8844
rs8844
HOXB7 ; HOXB8 ; HOXB9
0.010 GeneticVariation BEFREE Our objective was to evaluate whether single nucleotide polymorphisms (SNPs) of HOXB9 (rs2303486 and rs8844) were associated with DDH i</span>n Chinese population. 24600698

2014
dbSNP: rs711819
rs711819
HOXD9
0.010 GeneticVariation BEFREE Comparing the genotypic distribution of rs711819, there was significant differences between DDH patients group and control group (χ² = 7.54, df =2, P =0.023), and the association to DDH developing reached significance (P =0.045, OR =1.79, 95 % CI: 1.01-3.17 by dominant mode). 22520331

2012
dbSNP: rs11718863
rs11718863
COL6A4P1
0.010 GeneticVariation BEFREE Three SNPs rs7639618, rs9864422 and rs11718863 (in DVWA) were genotyped using a Taqman 5' allelic discrimination assay on an ABI 7500 real-time polymerase chain reaction (PCR) instrument in 368 children who suffered from Developmental dysplasia of the hip and 508 control subjects, and analyzed their associations. 20238217

2011
dbSNP: rs7639618
rs7639618
COL6A4P1
0.010 GeneticVariation BEFREE Three SNPs rs7639618, rs9864422 and rs11718863 (in DVWA) were genotyped using a Taqman 5' allelic discrimination assay on an ABI 7500 real-time polymerase chain reaction (PCR) instrument in 368 children who suffered from Developmental dysplasia of the hip and 508 control subjects, and analyzed their associations. 20238217

2011
dbSNP: rs9864422
rs9864422
COL6A4P1
0.010 GeneticVariation BEFREE Three SNPs rs7639618, rs9864422 and rs11718863 (in DVWA) were genotyped using a Taqman 5' allelic discrimination assay on an ABI 7500 real-time polymerase chain reaction (PCR) instrument in 368 children who suffered from Developmental dysplasia of the hip and 508 control subjects, and analyzed their associations. 20238217

2011
dbSNP: rs3744438
rs3744438
TBX4
0.010 GeneticVariation BEFREE Our objective is to evaluate whether the Tbx4 (rs3744438 and rs3744448) single nucleotide polymorphisms (SNPs) are associated with DDH in Chinese. 20887794

2010
dbSNP: rs3744448
rs3744448
TBX4
0.010 GeneticVariation BEFREE Our objective is to evaluate whether the Tbx4 (rs3744438 and rs3744448) single nucleotide polymorphisms (SNPs) are associated with DDH in Chinese. 20887794

2010
dbSNP: rs61746008
rs61746008
FBN1
0.010 GeneticVariation BEFREE Fibrillin 1 gene with R2726W mutation is absent in patients with primary protrusio acetabuli and developmental dysplasia of the hip. 19396033

2009