rs121913409, CTNNB1

N. diseases: 21
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
CUI: C0025202
Disease: melanoma
515 0.708 0.400 3 41224646 missense variant C/A;G;T snv 0.700 1.000 8 1997 2014
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.708 0.400 3 41224646 missense variant C/A;G;T snv 0.010 1.000 1 2001 2001
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.708 0.400 3 41224646 missense variant C/A;G;T snv 0.050 1.000 5 2002 2019
Childhood Kidney Wilms Tumor
CUI: C1333015
Disease: Childhood Kidney Wilms Tumor
36 0.708 0.400 3 41224646 missense variant C/A;G;T snv 0.010 1.000 1 2002 2002
Nephroblastoma
CUI: C0027708
Disease: Nephroblastoma
125 0.708 0.400 3 41224646 missense variant C/A;G;T snv 0.010 1.000 1 2002 2002
Fibromatosis, Aggressive
CUI: C0079218
Disease: Fibromatosis, Aggressive
12 0.708 0.400 3 41224646 missense variant C/A;G;T snv 0.090 1.000 9 2013 2019
Malignant neoplasm of soft tissue
CUI: C4551686
Disease: Malignant neoplasm of soft tissue
32 0.708 0.400 3 41224646 missense variant C/A;G;T snv 0.010 1.000 1 2015 2015
Sarcoma
CUI: C1261473
Disease: Sarcoma
42 0.708 0.400 3 41224646 missense variant C/A;G;T snv 0.010 1.000 1 2015 2015
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.708 0.400 3 41224646 missense variant C/A;G;T snv 0.820 1.000 3 2016 2018
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.708 0.400 3 41224646 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Adenocarcinoma of prostate
CUI: C0007112
Disease: Adenocarcinoma of prostate
108 0.708 0.400 3 41224646 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Adrenocortical carcinoma
CUI: C0206686
Disease: Adrenocortical carcinoma
46 0.708 0.400 3 41224646 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.708 0.400 3 41224646 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.708 0.400 3 41224646 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Malignant Uterine Corpus Neoplasm
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
152 0.708 0.400 3 41224646 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Neuromuscular hamartoma
CUI: C0346056
Disease: Neuromuscular hamartoma
2 0.708 0.400 3 41224646 missense variant C/A;G;T snv 0.010 1.000 1 2016 2016
Transitional cell carcinoma of bladder
158 0.708 0.400 3 41224646 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Adenoma
CUI: C0001430
Disease: Adenoma
103 0.708 0.400 3 41224646 missense variant C/A;G;T snv 0.010 1.000 1 2017 2017
Paranasal sinus teratocarcinosarcoma (type)
1 0.708 0.400 3 41224646 missense variant C/A;G;T snv 0.010 1.000 1 2017 2017
Solid Neoplasm
CUI: C0280100
Disease: Solid Neoplasm
24 0.708 0.400 3 41224646 missense variant C/A;G;T snv 0.010 1.000 1 2017 2017
Hepatoblastoma
CUI: C0206624
Disease: Hepatoblastoma
22 0.708 0.400 3 41224646 missense variant C/A;G;T snv 0.010 1.000 1 2019 2019