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: rs747126003
rs747126003
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C0028754
Disease: Obesity
Obesity
0.020 0.500 2 2009 2012
dbSNP: rs747126003
rs747126003
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
0.010 < 0.001 1 2012 2012
dbSNP: rs747126003
rs747126003
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site
0.010 1.000 1 2017 2017
dbSNP: rs747126003
rs747126003
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C1719672
Disease: Severe Sepsis
Severe Sepsis
0.010 1.000 1 2006 2006
dbSNP: rs747126003
rs747126003
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C0036690
Disease: Septicemia
Septicemia
0.010 1.000 1 2006 2006
dbSNP: rs747126003
rs747126003
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C0278996
Disease: Malignant Head and Neck Neoplasm
Malignant Head and Neck Neoplasm
0.010 1.000 1 2007 2007
dbSNP: rs747126003
rs747126003
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C3496337
Disease: Idiopathic Nephrotic Syndrome
Idiopathic Nephrotic Syndrome
0.010 1.000 1 2017 2017
dbSNP: rs747126003
rs747126003
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C3887461
Disease: Head and Neck Carcinoma
Head and Neck Carcinoma
0.010 1.000 1 2007 2007
dbSNP: rs747126003
rs747126003
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C3826128
Disease: Infection in children
Infection in children
0.010 1.000 1 2017 2017
dbSNP: rs747126003
rs747126003
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
0.010 < 0.001 1 2012 2012
dbSNP: rs747126003
rs747126003
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C0243026
Disease: Sepsis
Sepsis
0.010 1.000 1 2006 2006
dbSNP: rs747126003
rs747126003
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C0585442
Disease: Osteosarcoma of bone
Osteosarcoma of bone
0.010 < 0.001 1 2017 2017
dbSNP: rs747126003
rs747126003
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C1533172
Disease: Infantile nystagmus syndrome
Infantile nystagmus syndrome
0.010 1.000 1 2017 2017
dbSNP: rs747126003
rs747126003
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C0029463
Disease: Osteosarcoma
Osteosarcoma
0.010 < 0.001 1 2017 2017
dbSNP: rs747126003
rs747126003
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.010 1.000 1 2019 2019
dbSNP: rs747126003
rs747126003
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
0.010 < 0.001 1 2012 2012
dbSNP: rs747126003
rs747126003
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C1332986
Disease: Childhood Osteosarcoma
Childhood Osteosarcoma
0.010 < 0.001 1 2017 2017
dbSNP: rs747126003
rs747126003
0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06
CUI: C1704321
Disease: Nephrotic Syndrome, Minimal Change
Nephrotic Syndrome, Minimal Change
0.010 1.000 1 2017 2017