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: rs2010963
rs2010963
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2014 2014
dbSNP: rs2010963
rs2010963
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
CUI: C0278678
Disease: Metastatic Renal Cell Cancer
Metastatic Renal Cell Cancer
0.010 1.000 1 2017 2017
dbSNP: rs2010963
rs2010963
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
CUI: C0027092
Disease: Myopia
Myopia
0.010 1.000 1 2012 2012
dbSNP: rs2010963
rs2010963
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot
0.010 1.000 1 2015 2015
dbSNP: rs2010963
rs2010963
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.010 < 0.001 1 2014 2014
dbSNP: rs2010963
rs2010963
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
0.010 1.000 1 2015 2015
dbSNP: rs2010963
rs2010963
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2014 2014
dbSNP: rs2010963
rs2010963
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.010 1.000 1 2016 2016
dbSNP: rs2010963
rs2010963
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
Lip and Oral Cavity Carcinoma
0.010 1.000 1 2012 2012
dbSNP: rs2010963
rs2010963
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
0.010 1.000 1 2019 2019
dbSNP: rs2010963
rs2010963
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
CUI: C0751075
Disease: Cancer of Digestive System
Cancer of Digestive System
0.010 1.000 1 2014 2014
dbSNP: rs2010963
rs2010963
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth
0.010 1.000 1 2012 2012
dbSNP: rs2010963
rs2010963
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.010 1.000 1 2020 2020
dbSNP: rs2010963
rs2010963
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
CUI: C0042345
Disease: Varicosity
Varicosity
0.010 1.000 1 2018 2018
dbSNP: rs2010963
rs2010963
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
Palmar-plantar erythrodysesthesia syndrome
0.010 1.000 1 2016 2016
dbSNP: rs2010963
rs2010963
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
CUI: C3714636
Disease: Pneumonitis
Pneumonitis
0.010 1.000 1 2012 2012
dbSNP: rs2010963
rs2010963
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix
0.010 1.000 1 2015 2015
dbSNP: rs2010963
rs2010963
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
CUI: C0009375
Disease: Colonic Neoplasms
Colonic Neoplasms
0.010 1.000 1 2014 2014
dbSNP: rs2010963
rs2010963
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
CUI: C0206733
Disease: Strawberry nevus of skin
Strawberry nevus of skin
0.010 1.000 1 2018 2018
dbSNP: rs2010963
rs2010963
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
CUI: C1332986
Disease: Childhood Osteosarcoma
Childhood Osteosarcoma
0.010 1.000 1 2014 2014
dbSNP: rs2010963
rs2010963
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
CUI: C0029463
Disease: Osteosarcoma
Osteosarcoma
0.010 1.000 1 2014 2014
dbSNP: rs2010963
rs2010963
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.010 < 0.001 1 2019 2019
dbSNP: rs2010963
rs2010963
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.010 1.000 1 2016 2016
dbSNP: rs2010963
rs2010963
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
0.010 1.000 1 2015 2015
dbSNP: rs2010963
rs2010963
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
CUI: C0039483
Disease: Giant Cell Arteritis
Giant Cell Arteritis
0.010 1.000 1 2005 2005