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: rs156697
rs156697
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.030 1.000 3 2010 2017
dbSNP: rs156697
rs156697
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.030 1.000 3 2010 2017
dbSNP: rs156697
rs156697
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.020 1.000 2 2010 2016
dbSNP: rs156697
rs156697
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35
CUI: C0036646
Disease: Age-related cataract
Age-related cataract
0.020 1.000 2 2014 2016
dbSNP: rs156697
rs156697
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35
Malignant neoplasm of urinary bladder
0.020 1.000 2 2012 2015
dbSNP: rs156697
rs156697
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder
0.020 1.000 2 2012 2015
dbSNP: rs156697
rs156697
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35
Clear-cell metastatic renal cell carcinoma
0.010 1.000 1 2018 2018
dbSNP: rs156697
rs156697
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2011 2011
dbSNP: rs156697
rs156697
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35
CUI: C1861305
Disease: TARSAL-CARPAL COALITION SYNDROME
TARSAL-CARPAL COALITION SYNDROME
0.010 1.000 1 2015 2015
dbSNP: rs156697
rs156697
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
0.010 1.000 1 2018 2018
dbSNP: rs156697
rs156697
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.010 1.000 1 2016 2016
dbSNP: rs156697
rs156697
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
Carcinoma, Ovarian Epithelial
0.010 1.000 1 2010 2010
dbSNP: rs156697
rs156697
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35
Conventional (Clear Cell) Renal Cell Carcinoma
0.010 1.000 1 2018 2018
dbSNP: rs156697
rs156697
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35
CUI: C1140680
Disease: Malignant neoplasm of ovary
Malignant neoplasm of ovary
0.010 1.000 1 2010 2010
dbSNP: rs156697
rs156697
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 1.000 1 2011 2011
dbSNP: rs156697
rs156697
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35
CUI: C0004096
Disease: Asthma
Asthma
0.010 1.000 1 2014 2014
dbSNP: rs156697
rs156697
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm
0.010 1.000 1 2010 2010
dbSNP: rs156697
rs156697
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2011 2011
dbSNP: rs156697
rs156697
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
0.010 1.000 1 2009 2009
dbSNP: rs156697
rs156697
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35
CUI: C0037284
Disease: Skin lesion
Skin lesion
0.010 1.000 1 2018 2018
dbSNP: rs156697
rs156697
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
0.010 1.000 1 2012 2012
dbSNP: rs156697
rs156697
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35
Precursor B-cell lymphoblastic leukemia
0.010 < 0.001 1 2015 2015
dbSNP: rs156697
rs156697
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35
Malignant neoplasm of colon and/or rectum
0.010 1.000 1 2011 2011
dbSNP: rs156697
rs156697
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma
0.010 < 0.001 1 2015 2015
dbSNP: rs156697
rs156697
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35
CUI: C0524851
Disease: Neurodegenerative Disorders
Neurodegenerative Disorders
0.010 1.000 1 2018 2018