RELN, reelin, 5649

N. diseases: 178; N. variants: 52
Disease: Otosclerosis ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3914132
rs3914132
Entrez Id: 5649
Gene Symbol: RELN
RELN
CUI: C0029899
Disease:
Otosclerosis 		0.810 GeneticVariation BEFREE Recently, a reelin gene, SNP rs3914132, located in intron 2, was shown to be associated with otosclerosis in a European population. 20882487 2010
dbSNP: rs3914132
rs3914132
Entrez Id: 5649
Gene Symbol: RELN
RELN
CUI: C0029899
Disease:
Otosclerosis 		0.810 GeneticVariation GWASDB A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis. 19230858 2009
dbSNP: rs3914132
rs3914132
Entrez Id: 5649
Gene Symbol: RELN
RELN
CUI: C0029899
Disease:
Otosclerosis 		0.810 GeneticVariation GWASCAT A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis. 19230858 2009