Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2476601
rs2476601
PTPN22 ; AP4B1-AS1
0.010 GeneticVariation BEFREE Gender-specific association of the PTPN22 C1858T polymorphism with achalasia. 17961776

2007