rs477992, PHGDH

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.
Amino acids measurement
CUI: C0201874
Disease: Amino acids measurement
92 1 119714953 intron variant A/G snv 0.69 0.700 1.000 1 2015 2015
elevated blood glucose level
CUI: C0495706
Disease: elevated blood glucose level
111 1 119714953 intron variant A/G snv 0.69 0.700 1.000 1 2011 2011
Glucose measurement
CUI: C0337438
Disease: Glucose measurement
111 1 119714953 intron variant A/G snv 0.69 0.700 1.000 1 2011 2011
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 1 119714953 intron variant A/G snv 0.69 0.700 1.000 1 2018 2018