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: rs11171806
rs11171806
0.807 0.360 12 56339747 synonymous variant G/A snv 4.9E-02 4.5E-02
CUI: C0003872
Disease: Arthritis, Psoriatic
Arthritis, Psoriatic
0.010 1.000 1 2013 2013
dbSNP: rs11171806
rs11171806
0.807 0.360 12 56339747 synonymous variant G/A snv 4.9E-02 4.5E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.010 1.000 1 2019 2019
dbSNP: rs11171806
rs11171806
0.807 0.360 12 56339747 synonymous variant G/A snv 4.9E-02 4.5E-02
CUI: C0018213
Disease: Graves Disease
Graves Disease
0.010 1.000 1 2015 2015
dbSNP: rs11171806
rs11171806
0.807 0.360 12 56339747 synonymous variant G/A snv 4.9E-02 4.5E-02
CUI: C0311370
Disease: Lupus anticoagulant disorder
Lupus anticoagulant disorder
0.010 1.000 1 2016 2016
dbSNP: rs11171806
rs11171806
0.807 0.360 12 56339747 synonymous variant G/A snv 4.9E-02 4.5E-02
CUI: C0020459
Disease: Hyperinsulinism
Hyperinsulinism
0.010 1.000 1 2019 2019
dbSNP: rs11171806
rs11171806
0.807 0.360 12 56339747 synonymous variant G/A snv 4.9E-02 4.5E-02
Diabetes Mellitus, Insulin-Dependent
0.010 1.000 1 2013 2013
dbSNP: rs11171806
rs11171806
0.807 0.360 12 56339747 synonymous variant G/A snv 4.9E-02 4.5E-02
Premature coronary artery atherosclerosis
0.010 1.000 1 2019 2019
dbSNP: rs79824801
rs79824801
1.000 0.040 12 56334353 intron variant T/C snv 4.5E-02
Experimental Organism Basal Cell Carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs79824801
rs79824801
1.000 0.040 12 56334353 intron variant T/C snv 4.5E-02
CUI: C4721806
Disease: Carcinoma, Basal Cell
Carcinoma, Basal Cell
0.010 1.000 1 2017 2017