Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397514511
rs397514511
INPPL1
0.800 GeneticVariation UNIPROT Exome sequencing identifies INPPL1 mutations as a cause of opsismodysplasia. 23273569

2013
dbSNP: rs397514511
rs397514511
INPPL1
T 0.800 CausalMutation CLINVAR