rs892295, CHL1

N. diseases: 4
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 3 355870 intron variant A/G snv 0.87 0.700 1.000 1 2012 2012
Aspartate aminotransferase measurement
CUI: C0201899
Disease: Aspartate aminotransferase measurement
76 3 355870 intron variant A/G snv 0.87 0.700 1.000 1 2012 2012
Polysomnography
CUI: C0162701
Disease: Polysomnography
249 3 355870 intron variant A/G snv 0.87 0.700 1.000 1 2012 2012
Serum Alanine Aminotransferase Measurement
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
77 3 355870 intron variant A/G snv 0.87 0.700 1.000 1 2012 2012