rs588682, DLGAP1

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.
Alanine measurement
CUI: C0523459
Disease: Alanine measurement
3 18 3558080 intron variant G/A snv 0.71 0.700 1.000 1 2019 2019
Amino acids measurement
CUI: C0201874
Disease: Amino acids measurement
92 18 3558080 intron variant G/A snv 0.71 0.700 1.000 1 2019 2019