rs1057518914, RPS6KA3

N. diseases: 14
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Mitral Valve Prolapse Syndrome
CUI: C0026267
Disease: Mitral Valve Prolapse Syndrome
0.700 GeneticVariation CLINVAR
Deformity of lower limb
CUI: C1096086
Disease: Deformity of lower limb
0.700 GeneticVariation CLINVAR
Specific learning disability
CUI: C4025790
Disease: Specific learning disability
0.700 GeneticVariation CLINVAR
Orbital separation excessive
CUI: C0020534
Disease: Orbital separation excessive
0.700 GeneticVariation CLINVAR
Low posterior hairline
CUI: C1855728
Disease: Low posterior hairline
0.700 GeneticVariation CLINVAR
Acid reflux
CUI: C4317146
Disease: Acid reflux
0.700 GeneticVariation CLINVAR
Micrognathism
CUI: C0025990
Disease: Micrognathism
0.700 GeneticVariation CLINVAR
Low set ears
CUI: C0239234
Disease: Low set ears
0.700 GeneticVariation CLINVAR
Thoracolumbar scoliosis
CUI: C0749379
Disease: Thoracolumbar scoliosis
0.700 GeneticVariation CLINVAR
Ventricular Septal Defects
CUI: C0018818
Disease: Ventricular Septal Defects
0.700 GeneticVariation CLINVAR
Deep philtrum
CUI: C1839797
Disease: Deep philtrum
0.700 GeneticVariation CLINVAR
Low anterior hairline
CUI: C1842366
Disease: Low anterior hairline
0.700 GeneticVariation CLINVAR
Triangular face
CUI: C1835884
Disease: Triangular face
0.700 GeneticVariation CLINVAR
Clinodactyly
CUI: C4551485
Disease: Clinodactyly
0.700 GeneticVariation CLINVAR