Source: GWASCAT

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: rs4711350
rs4711350
LEMD2
1.000 0.040 6 33773939 intron variant A/G snv 0.79
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 2 2015 2019
dbSNP: rs5875463
rs5875463
MLN ; LEMD2 ; LOC105375024
6 33795960 intron variant TTT/-;T;TT;TTTT;TTTTT;TTTTTT delins
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018