rs1555601863, UNC13D

N. diseases: 5
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Histiocytosis haematophagic
CUI: C0876991
Disease: Histiocytosis haematophagic
0.700 GeneticVariation CLINVAR
Hepatomegaly
CUI: C0019209
Disease: Hepatomegaly
0.700 GeneticVariation CLINVAR
Unexplained fevers
CUI: C1844662
Disease: Unexplained fevers
0.700 GeneticVariation CLINVAR
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 3
CUI: C1837174
Disease: HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 3
0.700 GeneticVariation CLINVAR
Reduced natural killer cell activity
CUI: C1839969
Disease: Reduced natural killer cell activity
0.700 GeneticVariation CLINVAR