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: rs1129055
rs1129055
0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25
CUI: C0243026
Disease: Sepsis
Sepsis
0.020 0.500 2 2018 2019
dbSNP: rs1129055
rs1129055
0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25
CUI: C0036690
Disease: Septicemia
Septicemia
0.020 0.500 2 2018 2019
dbSNP: rs1129055
rs1129055
0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25
CUI: C0030809
Disease: Pemphigus Vulgaris
Pemphigus Vulgaris
0.010 1.000 1 2017 2017
dbSNP: rs1129055
rs1129055
0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.010 1.000 1 2010 2010
dbSNP: rs1129055
rs1129055
0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2014 2014
dbSNP: rs1129055
rs1129055
0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.010 1.000 1 2012 2012
dbSNP: rs1129055
rs1129055
0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25
CUI: C0006309
Disease: Brucellosis
Brucellosis
0.010 1.000 1 2014 2014
dbSNP: rs1129055
rs1129055
0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2014 2014
dbSNP: rs1129055
rs1129055
0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25
CUI: C0346647
Disease: Malignant neoplasm of pancreas
Malignant neoplasm of pancreas
0.010 1.000 1 2012 2012
dbSNP: rs1129055
rs1129055
0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25
CUI: C0263313
Disease: Pemphigus Foliaceus
Pemphigus Foliaceus
0.010 1.000 1 2017 2017
dbSNP: rs1129055
rs1129055
0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
0.010 1.000 1 2010 2010
dbSNP: rs1129055
rs1129055
0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.010 1.000 1 2013 2013
dbSNP: rs1129055
rs1129055
0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25
Malignant neoplasm of colon and/or rectum
0.010 1.000 1 2014 2014
dbSNP: rs1129055
rs1129055
0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25
CUI: C0856825
Disease: Acute GVH disease
Acute GVH disease
0.010 1.000 1 2018 2018
dbSNP: rs1129055
rs1129055
0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2014 2014