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: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia
0.100 0.943 35 2001 2019
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.100 0.813 32 2004 2019
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.100 0.813 32 2004 2019
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.100 0.806 31 2002 2019
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
Childhood Acute Lymphoblastic Leukemia
0.100 0.871 31 2005 2019
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
Adult Acute Lymphocytic Leukemia
0.100 0.931 29 2002 2019
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 1.000 24 2002 2018
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
Malignant neoplasm of colon and/or rectum
0.100 0.870 23 2002 2018
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C4521042
Disease: Complete Trisomy 21 Syndrome
Complete Trisomy 21 Syndrome
0.100 0.857 21 2003 2019
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.100 0.905 21 2004 2018
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0598608
Disease: Hyperhomocysteinemia
Hyperhomocysteinemia
0.100 0.762 21 2000 2018
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0027794
Disease: Neural Tube Defects
Neural Tube Defects
0.100 0.667 21 1999 2019
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0013080
Disease: Down Syndrome
Down Syndrome
0.100 0.857 21 2003 2019
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.100 1.000 20 2002 2018
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.100 0.895 19 2001 2018
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.100 0.684 19 2005 2020
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0021364
Disease: Male infertility
Male infertility
0.100 0.688 16 2005 2019
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.100 0.800 15 2001 2020
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.100 0.917 12 2000 2019
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.100 0.833 12 2005 2014
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.100 0.727 11 2004 2016
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.100 0.727 11 2004 2016
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.100 1.000 11 2000 2019
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke
0.100 0.909 11 2006 2018
dbSNP: rs397507444
rs397507444
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.100 0.818 11 2005 2014