Disease: Hirschsprung Disease ×
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