Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs373799938
rs373799938
CUI: C0700639
Disease: Pyloric Stenosis, Hypertrophic
Pyloric Stenosis, Hypertrophic 		0.700 GeneticVariation GWASDB Common variants near MBNL1 and NKX2-5 are associated with infantile hypertrophic pyloric stenosis. 22306654

2012