Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs77743549
rs77743549
Entrez Id: 11185;100526825
Gene Symbol: INMT;INMT-MINDY4
INMT;INMT-MINDY4
CUI: C0019569
Disease:
Hirschsprung Disease 		0.010 GeneticVariation BEFREE Although further replications and functional evaluations are needed, our study suggests that rs77743549 of INMT may be associated with the risk for HSCR and/or the development of the enteric nervous system. 26183064 2015
dbSNP: rs255163
rs255163
Entrez Id: 11185;105375219;105375220
Gene Symbol: INMT;LOC105375219;LOC105375220
INMT;LOC105375219;LOC105375220
CUI: C1269683
Disease:
Major Depressive Disorder 		0.010 GeneticVariation BEFREE To explore the possible relationship between six single nucleotide polymorphisms (SNPs) (rs6311 and rs6305 of 5-HT2A, rs5443 of Gβ3, rs2230739 of ACDY9, rs1549870 of PDE1A and rs255163 of CREB1, which are all related with 5-HT2A the signal transduction pathway) and the response efficacy to selective serotonin reuptake inhibitor (SSRI) treatments in major depressive disorder (MDD) Chinese. 22480177 2012