Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1158061584
rs1158061584
Entrez Id: 10443
Gene Symbol: N4BP2L2
N4BP2L2
CUI: C0349588
Disease:
Short stature
AT 0.700 CausalMutation CLINVAR