STMN1, stathmin 1, 3925

N. diseases: 284; N. variants: 1
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs182455
rs182455
Entrez Id: 3925;105376885
Gene Symbol: STMN1;LOC105376885
STMN1;LOC105376885
CUI: C0038436
Disease:
Post-Traumatic Stress Disorder 		0.010 GeneticVariation BEFREE This study examined the association between STMN1 rs182455 genotype, a single nucleotide polymorphism (SNP) located within or close to the putative transcriptional control region of STMN1 gene, and PTSD symptoms. 23583473 2013
dbSNP: rs182455
rs182455
Entrez Id: 3925;105376885
Gene Symbol: STMN1;LOC105376885
STMN1;LOC105376885
CUI: C0026769
Disease:
Multiple Sclerosis 		0.010 GeneticVariation BEFREE We conclude that despite potential importance of stathmin in the pathogenesis of MS, the rs182455 polymorphism does not influence MS susceptibility or clinical disease course. 19012073 2008