MLXIPL, MLX interacting protein like, 51085

N. diseases: 165; N. variants: 29
Disease: Coronary heart disease ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs35493868
rs35493868 		1.000 0.040 7 73625076 upstream gene variant C/G;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs3812316
rs3812316 		0.763 0.240 7 73606007 missense variant C/G snv 0.10 9.4E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.010 1.000 1 2015 2015