SYNRG, synergin gamma, 11276

N. diseases: 2; N. variants: 2
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3110628
rs3110628
Entrez Id: 11276
Gene Symbol: SYNRG
SYNRG
CUI: C0596887
Disease:
mathematical ability 		C 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs4262994
rs4262994
Entrez Id: 11276
Gene Symbol: SYNRG
SYNRG
CUI: C0041296
Disease:
Tuberculosis 		0.010 GeneticVariation BEFREE The present study reported for the first time that the rs12939622, rs4262994 and rs2542670 genotypes in lnc-HNF1B-3:1 locus may influence the clinical manifestations of tuberculosis. 31692082 2020
dbSNP: rs4262994
rs4262994
Entrez Id: 11276
Gene Symbol: SYNRG
SYNRG
CUI: C0015967
Disease:
Fever 		0.010 GeneticVariation BEFREE The AA genotype of rs12939622 (in the dominant model) and the AA genotype of rs4262994 (in the recessive model) caused increased susceptibility of the subjects to fever (P < .001 and P = .008, respectively). 31692082 2020