rs2239612, ST6GAL1

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.
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 1.000 0.040 3 187075454 intron variant G/A snv 0.17 0.800 1.000 1 2012 2012
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 1.000 0.040 3 187075454 intron variant G/A snv 0.17 0.700 1.000 1 2012 2012