Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121912889
rs121912889
C 0.710 CausalMutation CLINVAR

dbSNP: rs121912886
rs121912886
A 0.700 GeneticVariation CLINVAR Double heterozygosity for pseudoachondroplasia and spondyloepiphyseal dysplasia congenita. 11746045

2001

dbSNP: rs121912874
rs121912874
A 0.700 CausalMutation CLINVAR

dbSNP: rs121912880
rs121912880
T 0.700 CausalMutation CLINVAR

dbSNP: rs121912890
rs121912890
T 0.700 CausalMutation CLINVAR

dbSNP: rs121912893
rs121912893
A 0.700 CausalMutation CLINVAR

dbSNP: rs1565664375
rs1565664375
G 0.700 CausalMutation CLINVAR

dbSNP: rs794727261
rs794727261
T 0.700 CausalMutation CLINVAR