rs11547328, CDK4

N. diseases: 27
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.
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 3
3 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 0.800 1.000 5 1995 2013
Hereditary Melanoma
CUI: C1512419
Disease: Hereditary Melanoma
67 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 0.710 1.000 1 2001 2001
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 0.700 1.000 1 2016 2016
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 0.700 1.000 1 2016 2016
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 0.700 1.000 1 2016 2016
Neoplastic Syndromes, Hereditary
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
6387 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 0.700 0
melanoma
CUI: C0025202
Disease: melanoma
515 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 0.100 1.000 11 1997 2016
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 0.020 0.500 2 2002 2003
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 0.020 0.500 2 2002 2006
Compensatory Hyperinsulinemia
CUI: C1257965
Disease: Compensatory Hyperinsulinemia
2 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 0.010 1.000 1 2008 2008
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 0.010 1.000 1 2008 2008
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 0.010 1.000 1 2008 2008
Diabetes Mellitus, Insulin-Dependent
954 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 0.010 1.000 1 2004 2004
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 0.010 1.000 1 2006 2006
leukemia
CUI: C0023418
Disease: leukemia
144 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 0.010 1.000 1 2003 2003
Lymphoma
CUI: C0024299
Disease: Lymphoma
91 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 0.010 1.000 1 2012 2012
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 0.010 1.000 1 2002 2002
Mantle cell lymphoma
CUI: C4721414
Disease: Mantle cell lymphoma
19 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 0.010 1.000 1 2012 2012
Melanocytic nevus
CUI: C0027962
Disease: Melanocytic nevus
33 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 0.010 1.000 1 2002 2002
Melanoma, B16
CUI: C0004565
Disease: Melanoma, B16
1 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 0.010 1 2006 2006
Multiple tumors
CUI: C0260037
Disease: Multiple tumors
12 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 0.010 1.000 1 2001 2001
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 0.010 1.000 1 2006 2006
Obesity
CUI: C0028754
Disease: Obesity
1111 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 0.010 1.000 1 2008 2008
Papilloma
CUI: C0030354
Disease: Papilloma
27 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 0.010 1.000 1 2002 2002
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 0.010 1.000 1 2002 2002