NDN, necdin, MAGE family member, 4692

N. diseases: 124; N. variants: 2
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs370006648
rs370006648
Entrez Id: 4692
Gene Symbol: NDN
NDN
CUI: C0027627
Disease:
Neoplasm Metastasis 		0.010 GeneticVariation BEFREE These data demonstrate that NDN and the T50C allele regulate gene expression and metastasis efficiency. 26384308 2015
dbSNP: rs114077338
rs114077338
Entrez Id: 4692
Gene Symbol: NDN
NDN
CUI: C0162809
Disease:
Kallmann Syndrome 		0.010 GeneticVariation BEFREE A rare variant of necdin (p.V318A) was described in a family with Kallmann syndrome associated with a FGFR1 mutation. 21543378 2011