rs2273697, ABCC2

N. diseases: 11
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.776 0.360 10 99804058 missense variant G/A snv 0.19 0.19 0.060 1.000 6 2014 2018
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.776 0.360 10 99804058 missense variant G/A snv 0.19 0.19 0.010 1.000 1 2019 2019
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.776 0.360 10 99804058 missense variant G/A snv 0.19 0.19 0.010 1 2013 2013
Complex partial seizures
CUI: C0149958
Disease: Complex partial seizures
5 0.776 0.360 10 99804058 missense variant G/A snv 0.19 0.19 0.010 1.000 1 2013 2013
Drug Resistant Epilepsy
CUI: C1096063
Disease: Drug Resistant Epilepsy
35 0.776 0.360 10 99804058 missense variant G/A snv 0.19 0.19 0.010 1 2012 2012
Generalized seizures
CUI: C0234533
Disease: Generalized seizures
13 0.776 0.360 10 99804058 missense variant G/A snv 0.19 0.19 0.010 1.000 1 2014 2014
Intellectual Disability
CUI: C3714756
Disease: Intellectual Disability
159 0.776 0.360 10 99804058 missense variant G/A snv 0.19 0.19 0.010 1.000 1 2008 2008
Mental Retardation
CUI: C0025362
Disease: Mental Retardation
98 0.776 0.360 10 99804058 missense variant G/A snv 0.19 0.19 0.010 1.000 1 2008 2008
Myeloid Leukemia, Chronic
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
115 0.776 0.360 10 99804058 missense variant G/A snv 0.19 0.19 0.010 1.000 1 2014 2014
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.776 0.360 10 99804058 missense variant G/A snv 0.19 0.19 0.010 1.000 1 2019 2019
Seizures
CUI: C0036572
Disease: Seizures
553 0.776 0.360 10 99804058 missense variant G/A snv 0.19 0.19 0.010 1.000 1 2012 2012