Source: UNIPROT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1553446603
rs1553446603
NCAPH
CUI: C4693843
Disease: MICROCEPHALY 23, PRIMARY, AUTOSOMAL RECESSIVE
MICROCEPHALY 23, PRIMARY, AUTOSOMAL RECESSIVE 		0.700 GeneticVariation UNIPROT Mutations in genes encoding condensin complex proteins cause microcephaly through decatenation failure at mitosis. 27737959

2016