SLC6A4, solute carrier family 6 member 4, 6532

N. diseases: 440; N. variants: 28
Disease: Frontotemporal Lobar Degeneration ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4795541
rs4795541
Entrez Id: 6532;105371720
Gene Symbol: SLC6A4;LOC105371720
SLC6A4;LOC105371720
CUI: C0751072
Disease:
Frontotemporal Lobar Degeneration 		0.010 GeneticVariation BEFREE In summary, the rs4795541 might be important for FTLD susceptibility in the Italian population. 19020798 2008