Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs724159980
rs724159980
A 0.700 CausalMutation CLINVAR

dbSNP: rs1561231553
rs1561231553
C 0.700 CausalMutation CLINVAR

dbSNP: rs398124474
rs398124474
T 0.700 CausalMutation CLINVAR

dbSNP: rs587784052
rs587784052
C 0.700 CausalMutation CLINVAR

dbSNP: rs587784053
rs587784053
C 0.700 GeneticVariation CLINVAR

dbSNP: rs587784055
rs587784055
A 0.700 CausalMutation CLINVAR

dbSNP: rs587784056
rs587784056
T 0.700 CausalMutation CLINVAR

dbSNP: rs727503771
rs727503771
A 0.700 CausalMutation CLINVAR

dbSNP: rs797045785
rs797045785
AG 0.700 CausalMutation CLINVAR

dbSNP: rs797045786
rs797045786
GA 0.700 CausalMutation CLINVAR

dbSNP: rs797045787
rs797045787
ACT 0.700 CausalMutation CLINVAR

dbSNP: rs797045788
rs797045788
TT 0.700 GeneticVariation CLINVAR

dbSNP: rs797045789
rs797045789
ATT 0.700 CausalMutation CLINVAR

dbSNP: rs121918265
rs121918265
G 0.800 CausalMutation CLINVAR

dbSNP: rs121918268
rs121918268
G 0.800 CausalMutation CLINVAR

dbSNP: rs587784000
rs587784000
T 0.800 GeneticVariation CLINVAR

dbSNP: rs587784024
rs587784024
A 0.800 CausalMutation CLINVAR Genotype-phenotype correlations of 39 patients with Cornelia De Lange syndrome: the Dutch experience. 16236812

2006

dbSNP: rs587784024
rs587784024
A 0.800 CausalMutation CLINVAR Precocious sister chromatid separation (PSCS) in Cornelia de Lange syndrome. 16100726

2005

dbSNP: rs587784024
rs587784024
A 0.800 CausalMutation CLINVAR NIPBL Controls RNA Biogenesis to Prevent Activation of the Stress Kinase PKR. 26725122

2016

dbSNP: rs587784025
rs587784025
T 0.800 GeneticVariation CLINVAR

dbSNP: rs587784036
rs587784036
A 0.800 CausalMutation CLINVAR High rate of mosaicism in individuals with Cornelia de Lange syndrome. 23505322

2013

dbSNP: rs587784036
rs587784036
A 0.800 CausalMutation CLINVAR NIPBL mutational analysis in 120 individuals with Cornelia de Lange syndrome and evaluation of genotype-phenotype correlations. 15318302

2004

dbSNP: rs587784042
rs587784042
G 0.800 CausalMutation CLINVAR

dbSNP: rs80358376
rs80358376
T 0.800 CausalMutation CLINVAR Clinical score of 62 Italian patients with Cornelia de Lange syndrome and correlations with the presence and type of NIPBL mutation. 17661813

2007

dbSNP: rs80358376
rs80358376
T 0.800 CausalMutation CLINVAR NIPBL Controls RNA Biogenesis to Prevent Activation of the Stress Kinase PKR. 26725122

2016