Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs864309488
rs864309488
G 0.700 GeneticVariation CLINVAR De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. 26637980

2015

dbSNP: rs121918494
rs121918494
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1553284997
rs1553284997
C 0.700 CausalMutation CLINVAR

dbSNP: rs1557036768
rs1557036768
T 0.700 CausalMutation CLINVAR

dbSNP: rs28936415
rs28936415
A 0.700 CausalMutation CLINVAR

dbSNP: rs376103091
rs376103091
A 0.700 CausalMutation CLINVAR

dbSNP: rs376754460
rs376754460
A 0.700 GeneticVariation CLINVAR

dbSNP: rs387907141
rs387907141
T 0.700 CausalMutation CLINVAR

dbSNP: rs66527965
rs66527965
T 0.700 CausalMutation CLINVAR