rs1553496850, STAT1

N. diseases: 3
Disease: IMMUNODEFICIENCY 31A ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
IMMUNODEFICIENCY 31A
CUI: C4013950
Disease: IMMUNODEFICIENCY 31A
0.700 GeneticVariation CLINVAR Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype. 27114460 2016