Source: BEFREE

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: rs1800624
rs1800624
AGER ; PBX2
0.658 0.480 6 32184610 upstream gene variant A/G;T snv
CUI: C0342257
Disease: Complications of Diabetes Mellitus
Complications of Diabetes Mellitus 		0.010 1.000 1 2019 2019
dbSNP: rs1800624
rs1800624
AGER ; PBX2
0.658 0.480 6 32184610 upstream gene variant A/G;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.010 < 0.001 1 2015 2015
dbSNP: rs1800624
rs1800624
AGER ; PBX2
0.658 0.480 6 32184610 upstream gene variant A/G;T snv
CUI: C0018799
Disease: Heart Diseases
Heart Diseases 		0.010 1.000 1 2019 2019
dbSNP: rs1800624
rs1800624
AGER ; PBX2
0.658 0.480 6 32184610 upstream gene variant A/G;T snv
CUI: C0243026
Disease: Sepsis
Sepsis 		0.010 1.000 1 2017 2017
dbSNP: rs1800624
rs1800624
AGER ; PBX2
0.658 0.480 6 32184610 upstream gene variant A/G;T snv
CUI: C4529962
Disease: Fatty Liver Disease
Fatty Liver Disease 		0.010 1.000 1 2018 2018
dbSNP: rs1800624
rs1800624
AGER ; PBX2
0.658 0.480 6 32184610 upstream gene variant A/G;T snv
CUI: C2939419
Disease: Secondary Neoplasm
Secondary Neoplasm 		0.010 1.000 1 2017 2017
dbSNP: rs1800624
rs1800624
AGER ; PBX2
0.658 0.480 6 32184610 upstream gene variant A/G;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.010 1.000 1 2014 2014
dbSNP: rs1800624
rs1800624
AGER ; PBX2
0.658 0.480 6 32184610 upstream gene variant A/G;T snv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.010 1.000 1 2016 2016