rs527624522, EXT2

N. diseases: 5
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Osteopenia
CUI: C0029453
Disease: Osteopenia
0.700 GeneticVariation CLINVAR
Feeding difficulties
CUI: C0232466
Disease: Feeding difficulties
0.700 GeneticVariation CLINVAR
Microcephaly (physical finding)
CUI: C4551563
Disease: Microcephaly (physical finding)
0.700 GeneticVariation CLINVAR
SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME
CUI: C4225248
Disease: SEIZURES, SCOLIOSIS, AND MACROCEPHALY SYNDROME
0.700 GeneticVariation CLINVAR
Seizures
CUI: C0036572
Disease: Seizures
0.700 GeneticVariation CLINVAR