NIN, ninein, 51199

N. diseases: 52; N. variants: 7
Disease: SECKEL SYNDROME 7 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387907308
rs387907308
Entrez Id: 51199
Gene Symbol: NIN
NIN
CUI: C3553870
Disease:
SECKEL SYNDROME 7 		C 0.700 CausalMutation CLINVAR
dbSNP: rs747680111
rs747680111
Entrez Id: 51199
Gene Symbol: NIN
NIN
CUI: C3553870
Disease:
SECKEL SYNDROME 7 		C 0.700 CausalMutation CLINVAR