rs72664208, ABCC6

N. diseases: 7
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
0.700 GeneticVariation CLINVAR
Retinal Hemorrhage
CUI: C0035317
Disease: Retinal Hemorrhage
0.700 GeneticVariation CLINVAR
Papule
CUI: C0332563
Disease: Papule
0.700 GeneticVariation CLINVAR
Intermittent Claudication
CUI: C0021775
Disease: Intermittent Claudication
0.700 GeneticVariation CLINVAR
Angioid Streaks
CUI: C0002982
Disease: Angioid Streaks
0.700 GeneticVariation CLINVAR
Pseudoxanthoma Elasticum
CUI: C0033847
Disease: Pseudoxanthoma Elasticum
0.700 GeneticVariation CLINVAR
Abnormally lax or hyperextensible skin
CUI: C4024736
Disease: Abnormally lax or hyperextensible skin
0.700 GeneticVariation CLINVAR