Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs797044806
rs797044806
Entrez Id: 64132
Gene Symbol: XYLT2
XYLT2
CUI: C4225412
Disease:
Spondylo-ocular syndrome
GC 0.700 CausalMutation CLINVAR