NUP37, nucleoporin 37, 79023

N. diseases: 24; N. variants: 4
Disease: MICROCEPHALY 24, PRIMARY, AUTOSOMAL RECESSIVE ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs746341112
rs746341112
Entrez Id: 79023
Gene Symbol: NUP37
NUP37
CUI: C4748555
Disease:
MICROCEPHALY 24, PRIMARY, AUTOSOMAL RECESSIVE 		A 0.700 GeneticVariation CLINVAR Mutations in multiple components of the nuclear pore complex cause nephrotic syndrome. 30179222 2018