rs596406, CELF2

N. diseases: 1
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.
Aspartate aminotransferase measurement
CUI: C0201899
Disease: Aspartate aminotransferase measurement
76 10 11182702 intron variant T/C snv 0.15 0.700 1.000 1 2013 2013