rs2071286, NOTCH4

N. diseases: 12
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.
Cryoglobulinemia
CUI: C0010403
Disease: Cryoglobulinemia
7 0.752 0.280 6 32212119 intron variant C/T snv 0.17 0.700 1.000 1 2014 2014
Hepatitis C, Chronic
CUI: C0524910
Disease: Hepatitis C, Chronic
80 0.752 0.280 6 32212119 intron variant C/T snv 0.17 0.700 1.000 1 2014 2014
Pemphigus Vulgaris
CUI: C0030809
Disease: Pemphigus Vulgaris
39 0.752 0.280 6 32212119 intron variant C/T snv 0.17 0.700 1.000 1 2012 2012
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.752 0.280 6 32212119 intron variant C/T snv 0.17 0.700 1.000 1 2010 2010
Adult Lymphoma
CUI: C1332206
Disease: Adult Lymphoma
66 0.752 0.280 6 32212119 intron variant C/T snv 0.17 0.010 1.000 1 2017 2017
Benign Lymphoproliferative Disorder
CUI: C0746351
Disease: Benign Lymphoproliferative Disorder
3 0.752 0.280 6 32212119 intron variant C/T snv 0.17 0.010 1.000 1 2017 2017
Childhood Lymphoma
CUI: C1332979
Disease: Childhood Lymphoma
66 0.752 0.280 6 32212119 intron variant C/T snv 0.17 0.010 1.000 1 2017 2017
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.752 0.280 6 32212119 intron variant C/T snv 0.17 0.010 1.000 1 2017 2017
Lymphoma
CUI: C0024299
Disease: Lymphoma
91 0.752 0.280 6 32212119 intron variant C/T snv 0.17 0.010 1.000 1 2017 2017
Lymphoma, Non-Hodgkin
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
197 0.752 0.280 6 32212119 intron variant C/T snv 0.17 0.010 1.000 1 2017 2017
Lymphoproliferative Disorders
CUI: C0024314
Disease: Lymphoproliferative Disorders
14 0.752 0.280 6 32212119 intron variant C/T snv 0.17 0.010 1.000 1 2017 2017
Mixed cryoglobulinemia
CUI: C0543697
Disease: Mixed cryoglobulinemia
5 0.752 0.280 6 32212119 intron variant C/T snv 0.17 0.010 1.000 1 2017 2017