Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs762890408
rs762890408
PCNT
0.010 GeneticVariation BEFREE We identified 2 different variants in exon 38 from the <i>PCNT</i> gene shared between affected members from 2 different families with either IA or SAH (p.R2728C and p.V2811L). 30413633

2018