Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555743003
rs1555743003
A 0.700 CausalMutation CLINVAR Novel splicing mutation in the ASXL3 gene causing Bainbridge-Ropers syndrome. 27075689

2016

dbSNP: rs1060505029
rs1060505029
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060505030
rs1060505030
T 0.700 CausalMutation CLINVAR

dbSNP: rs121909628
rs121909628
A 0.700 GeneticVariation CLINVAR

dbSNP: rs121909636
rs121909636
A 0.700 GeneticVariation CLINVAR

dbSNP: rs121918459
rs121918459
G 0.700 CausalMutation CLINVAR

dbSNP: rs138952094
rs138952094
A 0.700 GeneticVariation CLINVAR

dbSNP: rs143862988
rs143862988
C 0.700 GeneticVariation CLINVAR

dbSNP: rs184758350
rs184758350
G 0.700 GeneticVariation CLINVAR

dbSNP: rs200088377
rs200088377
A 0.700 GeneticVariation CLINVAR

dbSNP: rs201195175
rs201195175
G 0.700 GeneticVariation CLINVAR

dbSNP: rs572115942
rs572115942
A 0.700 CausalMutation CLINVAR

dbSNP: rs727505366
rs727505366
T 0.700 GeneticVariation CLINVAR

dbSNP: rs727505367
rs727505367
C 0.700 GeneticVariation CLINVAR

dbSNP: rs727505368
rs727505368
T 0.700 GeneticVariation CLINVAR

dbSNP: rs727505369
rs727505369
C 0.700 GeneticVariation CLINVAR

dbSNP: rs727505370
rs727505370
G 0.700 GeneticVariation CLINVAR

dbSNP: rs727505371
rs727505371
T 0.700 GeneticVariation CLINVAR

dbSNP: rs727505372
rs727505372
T 0.700 GeneticVariation CLINVAR

dbSNP: rs727505373
rs727505373
C 0.700 GeneticVariation CLINVAR

dbSNP: rs727505374
rs727505374
A 0.700 GeneticVariation CLINVAR