Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs78311289
rs78311289
G 0.890 CausalMutation CLINVAR

dbSNP: rs121913105
rs121913105
T 0.730 CausalMutation CLINVAR

dbSNP: rs121913105
rs121913105
C 0.730 CausalMutation CLINVAR

dbSNP: rs121913116
rs121913116
T 0.700 CausalMutation CLINVAR Novel FGFR3 mutations creating cysteine residues in the extracellular domain of the receptor cause achondroplasia or severe forms of hypochondroplasia. 16912704

2006

dbSNP: rs121913101
rs121913101
C 0.700 CausalMutation CLINVAR

dbSNP: rs121913101
rs121913101
G 0.700 CausalMutation CLINVAR

dbSNP: rs121913101
rs121913101
A 0.700 CausalMutation CLINVAR

dbSNP: rs121913103
rs121913103
G 0.700 CausalMutation CLINVAR

dbSNP: rs121913103
rs121913103
C 0.700 CausalMutation CLINVAR

dbSNP: rs121913103
rs121913103
T 0.700 CausalMutation CLINVAR

dbSNP: rs121913479
rs121913479
T 0.700 CausalMutation CLINVAR

dbSNP: rs121913482
rs121913482
T 0.700 CausalMutation CLINVAR

dbSNP: rs121913483
rs121913483
G 0.700 CausalMutation CLINVAR

dbSNP: rs121913484
rs121913484
T 0.700 CausalMutation CLINVAR

dbSNP: rs121913485
rs121913485
G 0.700 CausalMutation CLINVAR

dbSNP: rs28931614
rs28931614
A 0.700 CausalMutation CLINVAR

dbSNP: rs28933068
rs28933068
G 0.700 CausalMutation CLINVAR

dbSNP: rs397515514
rs397515514
T 0.700 CausalMutation CLINVAR

dbSNP: rs4647924
rs4647924
G 0.700 CausalMutation CLINVAR