Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs751728
rs751728
MLN ; LEMD2 ; LOC105375024
1.000 0.040 6 33796256 intron variant C/T snv 0.37
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2014 2014
dbSNP: rs2274459
rs2274459
MLN ; LEMD2 ; LOC105375024
1.000 0.040 6 33794465 downstream gene variant G/A snv 0.12
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2012 2012