rs1564062144, HNRNPK

N. diseases: 7
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Aplasia/Hypoplasia of the corpus callosum
CUI: C1861866
Disease: Aplasia/Hypoplasia of the corpus callosum
0.700 GeneticVariation CLINVAR
Small for gestational age (disorder)
CUI: C0235991
Disease: Small for gestational age (disorder)
0.700 GeneticVariation CLINVAR
AU-KLINE SYNDROME
CUI: C4225274
Disease: AU-KLINE SYNDROME
0.700 GeneticVariation CLINVAR
Ventricular Septal Defects
CUI: C0018818
Disease: Ventricular Septal Defects
0.700 GeneticVariation CLINVAR
Intrauterine retardation
CUI: C1386048
Disease: Intrauterine retardation
0.700 GeneticVariation CLINVAR
Atrial Septal Defects
CUI: C0018817
Disease: Atrial Septal Defects
0.700 GeneticVariation CLINVAR
Central hypotonia
CUI: C1842364
Disease: Central hypotonia
0.700 GeneticVariation CLINVAR