CAV2, caveolin 2, 858

N. diseases: 96; N. variants: 14
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1052990
rs1052990
Entrez Id: 858
Gene Symbol: CAV2
CAV2
CUI: C0152136
Disease:
Low Tension Glaucoma
0.010 GeneticVariation BEFREE The frequency of the minor allele (G) of rs1052990 was significantly decreased in NTG cases compared with controls (P=0.014, OR=0.71), whereas NTG or POAG cases had a significantly higher frequency of the allele than controls in previous studies. 23743525 2013