Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs188675529
rs188675529
Entrez Id: 57215;80152
Gene Symbol: THAP11;CENPT
THAP11;CENPT
CUI: C4551563
Disease:
Microcephaly (physical finding)
G 0.700 GeneticVariation CLINVAR