rs11671653, DNM2

N. diseases: 2
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 1.000 0.040 19 10727810 intron variant G/A;T snv 0.700 1.000 1 2011 2011
Low density lipoprotein cholesterol measurement
1142 1.000 0.040 19 10727810 intron variant G/A;T snv 0.700 1.000 1 2011 2011