Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387906677
rs387906677
0.800 GeneticVariation UNIPROT Bent bone dysplasia-FGFR2 type, a distinct skeletal disorder, has deficient canonical FGF signaling. 22387015

2012

dbSNP: rs387906678
rs387906678
0.800 GeneticVariation UNIPROT Bent bone dysplasia-FGFR2 type, a distinct skeletal disorder, has deficient canonical FGF signaling. 22387015

2012

dbSNP: rs387906677
rs387906677
C 0.800 CausalMutation CLINVAR

dbSNP: rs387906678
rs387906678
C 0.800 CausalMutation CLINVAR

dbSNP: rs1057519044
rs1057519044
T 0.700 GeneticVariation CLINVAR

dbSNP: rs121913478
rs121913478
C 0.700 CausalMutation CLINVAR

dbSNP: rs121918487
rs121918487
T 0.700 CausalMutation CLINVAR

dbSNP: rs121918491
rs121918491
T 0.700 CausalMutation CLINVAR

dbSNP: rs1434545235
rs1434545235
C 0.700 CausalMutation CLINVAR

dbSNP: rs1554927408
rs1554927408
T 0.700 CausalMutation CLINVAR

dbSNP: rs77543610
rs77543610
C 0.700 CausalMutation CLINVAR

dbSNP: rs79184941
rs79184941
C 0.700 CausalMutation CLINVAR