Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs114925667
rs114925667
UBA5 ; NPHP3-ACAD11
CUI: C0549629
Disease: Abnormal delivery
Abnormal delivery 		A 0.700 CausalMutation CLINVAR

dbSNP: rs374052333
rs374052333
UBA5 ; NPHP3-ACAD11
CUI: C0549629
Disease: Abnormal delivery
Abnormal delivery 		T 0.700 GeneticVariation CLINVAR