Disease: Severe myopia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554121443
rs1554121443
Entrez Id: 8831;100847012
Gene Symbol: SYNGAP1;MIR5004
SYNGAP1;MIR5004
CUI: C0271183
Disease:
Severe myopia 		T 0.700 CausalMutation CLINVAR