Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs786205134
rs786205134
T 0.700 CausalMutation CLINVAR A novel phenotype in N-glycosylation disorders: Gillessen-Kaesbach-Nishimura skeletal dysplasia due to pathogenic variants in ALG9. 25966638

2016

dbSNP: rs1057518783
rs1057518783
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057518797
rs1057518797
TAGGACG 0.700 CausalMutation CLINVAR

dbSNP: rs1057518899
rs1057518899
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057518906
rs1057518906
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057518952
rs1057518952
AC 0.700 CausalMutation CLINVAR

dbSNP: rs1057518959
rs1057518959
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518969
rs1057518969
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057518976
rs1057518976
C 0.700 GeneticVariation CLINVAR

dbSNP: rs113624356
rs113624356
G 0.700 CausalMutation CLINVAR

dbSNP: rs1286585831
rs1286585831
T 0.700 CausalMutation CLINVAR

dbSNP: rs137852944
rs137852944
A 0.700 CausalMutation CLINVAR

dbSNP: rs137854521
rs137854521
CA 0.700 CausalMutation CLINVAR

dbSNP: rs1553827236
rs1553827236
A 0.700 CausalMutation CLINVAR

dbSNP: rs1553927823
rs1553927823
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555444249
rs1555444249
C 0.700 CausalMutation CLINVAR

dbSNP: rs1555446033
rs1555446033
G 0.700 CausalMutation CLINVAR

dbSNP: rs1555448106
rs1555448106
C 0.700 CausalMutation CLINVAR

dbSNP: rs1555450475
rs1555450475
CG 0.700 CausalMutation CLINVAR

dbSNP: rs1555452400
rs1555452400
G 0.700 CausalMutation CLINVAR

dbSNP: rs1555452653
rs1555452653
GC 0.700 CausalMutation CLINVAR

dbSNP: rs1555452876
rs1555452876
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1555454847
rs1555454847
G 0.700 CausalMutation CLINVAR

dbSNP: rs1555454915
rs1555454915
G 0.700 CausalMutation CLINVAR

dbSNP: rs1555459345
rs1555459345
G 0.700 GeneticVariation CLINVAR