Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1926320
rs1926320
Entrez Id: 9201
Gene Symbol: DCLK1
DCLK1
CUI: C0152136
Disease:
Low Tension Glaucoma
0.010 GeneticVariation BEFREE Although the rs10483727 (SIX1), rs1926320 (DCLK1), or rs12025126 (RERE) alone may not be sufficient for the development of POAG, the association of these SNPs with a phenotypic feature in patients with NTG or HTG suggests that these loci contribute to the pathogenesis of POAG. 22584021 2012