NTM, neurotrimin, 50863

N. diseases: 58; N. variants: 27
Disease: Hair Color ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1169275
rs1169275
Entrez Id: 50863
Gene Symbol: NTM
NTM
CUI: C0018498
Disease:
Hair Color 		T 0.700 GeneticVariation GWASCAT Genome-wide study of hair colour in UK Biobank explains most of the SNP heritability. 30531825 2018