rs12500824, SHROOM3

N. diseases: 3
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.
Alanine aminotransferase measurement
CUI: C0201836
Disease: Alanine aminotransferase measurement
77 1.000 0.040 4 76495474 intron variant A/G;T snv 0.700 1.000 1 2018 2018
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 1.000 0.040 4 76495474 intron variant A/G;T snv 0.700 1.000 1 2018 2018
Serum Alanine Aminotransferase Measurement
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
77 1.000 0.040 4 76495474 intron variant A/G;T snv 0.700 1.000 1 2018 2018