rs886039902, ANKRD11

N. diseases: 6
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Abnormality of cardiovascular system morphology
0.700 CausalMutation CLINVAR
Portal Hypertension
CUI: C0020541
Disease: Portal Hypertension
0.700 CausalMutation CLINVAR
KBG syndrome
CUI: C0220687
Disease: KBG syndrome
0.700 CausalMutation CLINVAR
KBG syndrome
CUI: C0220687
Disease: KBG syndrome
0.700 GeneticVariation CLINVAR
hearing impairment
CUI: C1384666
Disease: hearing impairment
0.700 CausalMutation CLINVAR
Esophageal Varices
CUI: C0014867
Disease: Esophageal Varices
0.700 CausalMutation CLINVAR
Large head (disorder)
CUI: C2243051
Disease: Large head (disorder)
0.700 CausalMutation CLINVAR