SYT9, synaptotagmin 9, 143425

N. diseases: 11; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10769780
rs10769780
Entrez Id: 143425
Gene Symbol: SYT9
SYT9
CUI: C0202177
Disease:
Phospholipid measurement 		0.800 GeneticVariation GWASDB Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations. 22359512 2012
dbSNP: rs10769780
rs10769780
Entrez Id: 143425
Gene Symbol: SYT9
SYT9
CUI: C0202177
Disease:
Phospholipid measurement 		0.800 GeneticVariation GWASCAT Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations. 22359512 2012
dbSNP: rs4369384
rs4369384
Entrez Id: 143425
Gene Symbol: SYT9
SYT9
CUI: C0200695
Disease:
Fetal hemoglobin determination 		0.700 GeneticVariation GWASDB Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. 18245381 2008
dbSNP: rs11041321
rs11041321
Entrez Id: 143425
Gene Symbol: SYT9
SYT9
CUI: C0018816
Disease:
Heart Septal Defects 		0.010 GeneticVariation BEFREE The intronic SYT9 variant rs11041321, which exhibits a significant genome-wide association with circulating homocysteine, was associated with the occurrence of CCSDs. 28834160 2017