rs603965, CCND1

N. diseases: 14
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.
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.732 0.440 11 69648142 splice region variant G/A snv 0.700 1.000 1 2013 2013
Glioma
CUI: C0017638
Disease: Glioma
353 0.732 0.440 11 69648142 splice region variant G/A snv 0.020 1.000 2 2017 2019
Adult Meningioma
CUI: C0278877
Disease: Adult Meningioma
30 0.732 0.440 11 69648142 splice region variant G/A snv 0.010 1.000 1 2019 2019
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.732 0.440 11 69648142 splice region variant G/A snv 0.010 1.000 1 2014 2014
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.732 0.440 11 69648142 splice region variant G/A snv 0.010 1.000 1 2019 2019
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.732 0.440 11 69648142 splice region variant G/A snv 0.010 1.000 1 2014 2014
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.732 0.440 11 69648142 splice region variant G/A snv 0.010 1.000 1 2016 2016
Lymphoma, Non-Hodgkin
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
197 0.732 0.440 11 69648142 splice region variant G/A snv 0.010 1.000 1 2006 2006
Malignant neoplasm of urinary bladder
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
316 0.732 0.440 11 69648142 splice region variant G/A snv 0.010 1.000 1 2014 2014
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.732 0.440 11 69648142 splice region variant G/A snv 0.010 1.000 1 2016 2016
Meningioma
CUI: C0025286
Disease: Meningioma
43 0.732 0.440 11 69648142 splice region variant G/A snv 0.010 1.000 1 2019 2019
Meningioma, benign, no ICD-O subtype
CUI: C1762616
Disease: Meningioma, benign, no ICD-O subtype
30 0.732 0.440 11 69648142 splice region variant G/A snv 0.010 1.000 1 2019 2019
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.732 0.440 11 69648142 splice region variant G/A snv 0.010 1.000 1 2019 2019
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C
CUI: C2752147
Disease: XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C
82 0.732 0.440 11 69648142 splice region variant G/A snv 0.010 1.000 1 2014 2014