Disease: Severe myopia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7331047
rs7331047
Entrez Id: 387911;542767
Gene Symbol: C1QTNF9B;PCOTH
C1QTNF9B;PCOTH
CUI: C0271183
Disease:
Severe myopia 		0.010 GeneticVariation BEFREE Furthermore, five additional SNPs (rs9510902, rs3794338, rs1886970, rs7325450, and rs7331047) in the same linkage disequilibrium (LD) block with rs9318086 also proved to be significantly associated with high myopia in the Han Chinese population; p values ranged from 5.46 × 10(-11) to 6.16 × 10(-16). 21640322 2011