NPHS1

Nephrosis 1, congenital, Finnish type (nephrin)
Diseases associated with this gene: NPHS1
LOVD Gene: NPHS1
NCBI Gene: NPHS1
Gene Home Reference: NPHS1
Ensembl gene: ENSG00000161270
Ensembl location: ENSG00000161270

OMIM gene: 602716
Download all NPHS1 variants in ATOM XML format.
Download all NPHS1 variants in tab-separated format.











 Finnish Variants

Filtered from source LSDB
Progress

 All Variants

Source LSDB
  NPHS1 - All Variants





FinDis has received funding from the Academy of Finland, Center of Excellence in Disease Genetics
and the European Community's Seventh Framework Programme (FP7/2007-2013) under grant agreement number 200754 - the GEN2PHEN project.