rs121913412, CTNNB1

N. diseases: 19
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.
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.724 0.280 3 41224633 missense variant A/C;G;T snv 0.070 1.000 7 1998 2019
Fibromatosis, Aggressive
CUI: C0079218
Disease: Fibromatosis, Aggressive
12 0.724 0.280 3 41224633 missense variant A/C;G;T snv 0.060 1.000 6 2015 2019
Fibromatosis
CUI: C0016048
Disease: Fibromatosis
5 0.724 0.280 3 41224633 missense variant A/C;G;T snv 0.020 1.000 2 2012 2013
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.724 0.280 3 41224633 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Adenocarcinoma of pancreas
CUI: C0281361
Disease: Adenocarcinoma of pancreas
138 0.724 0.280 3 41224633 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Adenocarcinoma of prostate
CUI: C0007112
Disease: Adenocarcinoma of prostate
108 0.724 0.280 3 41224633 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Adrenocortical carcinoma
CUI: C0206686
Disease: Adrenocortical carcinoma
46 0.724 0.280 3 41224633 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Carcinoma
CUI: C0007097
Disease: Carcinoma
103 0.724 0.280 3 41224633 missense variant A/C;G;T snv 0.010 1.000 1 1998 1998
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.724 0.280 3 41224633 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.724 0.280 3 41224633 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.724 0.280 3 41224633 missense variant A/C;G;T snv 0.800 1.000 1 2016 2016
Malignant neoplasm of soft tissue
CUI: C4551686
Disease: Malignant neoplasm of soft tissue
32 0.724 0.280 3 41224633 missense variant A/C;G;T snv 0.010 1.000 1 2015 2015
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.724 0.280 3 41224633 missense variant A/C;G;T snv 0.010 1.000 1 2018 2018
Malignant Uterine Corpus Neoplasm
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
152 0.724 0.280 3 41224633 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Neuromuscular hamartoma
CUI: C0346056
Disease: Neuromuscular hamartoma
2 0.724 0.280 3 41224633 missense variant A/C;G;T snv 0.010 1.000 1 2016 2016
Sarcoma
CUI: C1261473
Disease: Sarcoma
42 0.724 0.280 3 41224633 missense variant A/C;G;T snv 0.010 1.000 1 2015 2015
Tumor Cell Invasion
CUI: C1269955
Disease: Tumor Cell Invasion
169 0.724 0.280 3 41224633 missense variant A/C;G;T snv 0.010 1.000 1 2019 2019
Desmoid Tumor Caused By Somatic Mutation
1 0.724 0.280 3 41224633 missense variant A/C;G;T snv 0.700 0
Hepatoblastoma
CUI: C0206624
Disease: Hepatoblastoma
22 0.724 0.280 3 41224633 missense variant A/C;G;T snv 0.700 0