Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121434488
rs121434488
PAFAH1B1
0.710 GeneticVariation BEFREE The two patients with posterior SBH harbored a missense (Arg241Pro) and a nonsense (R8X) mosaic mutation of LIS1. 14581661

2003
dbSNP: rs121434488
rs121434488
PAFAH1B1
C 0.710 CausalMutation CLINVAR

dbSNP: rs121434484
rs121434484
PAFAH1B1
C 0.700 CausalMutation CLINVAR

dbSNP: rs121434489
rs121434489
PAFAH1B1
T 0.700 CausalMutation CLINVAR