rs1800764, None

N. diseases: 10
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Neonatal Drug Withdrawal
CUI: C3540839
Disease: Neonatal Drug Withdrawal
0.010 GeneticVariation BEFREE Higher frequency of rs1799752 and rs1800764 homozygous mutant genotypes was seen in DN compared to DWN patients. 19787680 2009