Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554022725
rs1554022725
Entrez Id: 55325;441054
Gene Symbol: UFSP2;C4orf47
UFSP2;C4orf47
CUI: C1328407
Disease:
Hip Dysplasia
G 0.700 CausalMutation CLINVAR Novel spondyloepimetaphyseal dysplasia due to UFSP2 gene mutation. 28892125 2018