Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs17883901
rs17883901
GCLC
0.851 0.240 6 53545239 intron variant G/A;T snv 6.2E-02
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.020 1.000 2 2011 2019
dbSNP: rs17883901
rs17883901
GCLC
0.851 0.240 6 53545239 intron variant G/A;T snv 6.2E-02
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease 		0.010 1.000 1 2011 2011
dbSNP: rs17883901
rs17883901
GCLC
0.851 0.240 6 53545239 intron variant G/A;T snv 6.2E-02
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy 		0.010 1.000 1 2019 2019
dbSNP: rs17883901
rs17883901
GCLC
0.851 0.240 6 53545239 intron variant G/A;T snv 6.2E-02
CUI: C4082937
Disease: Necrotizing enterocolitis in fetus OR newborn
Necrotizing enterocolitis in fetus OR newborn 		0.010 < 0.001 1 2016 2016
dbSNP: rs17883901
rs17883901
GCLC
0.851 0.240 6 53545239 intron variant G/A;T snv 6.2E-02
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases 		0.010 1.000 1 2011 2011
dbSNP: rs17883901
rs17883901
GCLC
0.851 0.240 6 53545239 intron variant G/A;T snv 6.2E-02
CUI: C0342257
Disease: Complications of Diabetes Mellitus
Complications of Diabetes Mellitus 		0.010 1.000 1 2019 2019