Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs150404479
rs150404479
1.000 0.040 1 43222879 missense variant T/C snv 9.1E-03 9.8E-03
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2014 2014
dbSNP: rs150404479
rs150404479
1.000 0.040 1 43222879 missense variant T/C snv 9.1E-03 9.8E-03
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
Mental Disorders 0.700 1.000 1 2014 2014
dbSNP: rs621559
rs621559
0.827 0.080 1 43179740 intron variant G/A snv 0.18
Squamous cell carcinoma of esophagus
Digestive System Diseases; Neoplasms 0.020 1.000 2 2013 2014
dbSNP: rs621559
rs621559
0.827 0.080 1 43179740 intron variant G/A snv 0.18
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
Digestive System Diseases; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs621559
rs621559
0.827 0.080 1 43179740 intron variant G/A snv 0.18
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs621559
rs621559
0.827 0.080 1 43179740 intron variant G/A snv 0.18
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs621559
rs621559
0.827 0.080 1 43179740 intron variant G/A snv 0.18
CUI: C0017638
Disease: Glioma
Glioma
Neoplasms 0.010 1.000 1 2014 2014