SYT9, synaptotagmin 9, 143425

N. diseases: 11; N. variants: 3
Disease: Fetal hemoglobin determination ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
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