SLC2A4, solute carrier family 2 member 4, 6517

N. diseases: 158; N. variants: 7
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs5418
rs5418
1.000 0.040 17 7281773 5 prime UTR variant G/A snv 0.49
CUI: C0011847
Disease: Diabetes
Diabetes
Endocrine System Diseases 0.010 < 0.001 1 2011 2011
dbSNP: rs5421
rs5421
1.000 0.040 17 7285694 intron variant C/G snv
CUI: C0011847
Disease: Diabetes
Diabetes
Endocrine System Diseases 0.010 < 0.001 1 2011 2011
dbSNP: rs5435
rs5435
0.851 0.200 17 7283804 missense variant T/A;C snv 0.65
CUI: C0011847
Disease: Diabetes
Diabetes
Endocrine System Diseases 0.010 1.000 1 2011 2011