rs1057519381, MED12

N. diseases: 6
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Poor school performance
CUI: C1843367
Disease: Poor school performance
0.700 GeneticVariation CLINVAR
Micrognathism
CUI: C0025990
Disease: Micrognathism
0.700 GeneticVariation CLINVAR
Morphological abnormality of the semicircular canal
CUI: C4023386
Disease: Morphological abnormality of the semicircular canal
0.700 GeneticVariation CLINVAR
FG syndrome
CUI: C0220769
Disease: FG syndrome
0.700 GeneticVariation CLINVAR
Skewed maternal X inactivation
CUI: C4022856
Disease: Skewed maternal X inactivation
0.700 GeneticVariation CLINVAR
Pierre Robin Syndrome
CUI: C0031900
Disease: Pierre Robin Syndrome
0.700 GeneticVariation CLINVAR