rs59912467, STK11

N. diseases: 7
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.
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.790 0.120 19 1223126 missense variant C/G;T snv 5.2E-03; 4.1E-06 0.700 0
Central neuroblastoma
CUI: C0700095
Disease: Central neuroblastoma
231 0.790 0.120 19 1223126 missense variant C/G;T snv 5.2E-03; 4.1E-06 0.010 1.000 1 2015 2015
Childhood Neuroblastoma
CUI: C4086165
Disease: Childhood Neuroblastoma
231 0.790 0.120 19 1223126 missense variant C/G;T snv 5.2E-03; 4.1E-06 0.010 1.000 1 2015 2015
Cytogenetically normal acute myeloid leukemia
CUI: C3839868
Disease: Cytogenetically normal acute myeloid leukemia
9 0.790 0.120 19 1223126 missense variant C/G;T snv 5.2E-03; 4.1E-06 0.010 1.000 1 2018 2018
Mixed follicular and papillary thyroid carcinoma
CUI: C0346398
Disease: Mixed follicular and papillary thyroid carcinoma
8 0.790 0.120 19 1223126 missense variant C/G;T snv 5.2E-03; 4.1E-06 0.010 1.000 1 2015 2015
Neuroblastoma
CUI: C0027819
Disease: Neuroblastoma
386 0.790 0.120 19 1223126 missense variant C/G;T snv 5.2E-03; 4.1E-06 0.010 1.000 1 2015 2015
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
257 0.790 0.120 19 1223126 missense variant C/G;T snv 5.2E-03; 4.1E-06 0.010 1.000 1 2009 2009