rs121913407, CTNNB1

N. diseases: 12
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.
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.763 0.240 3 41224645 missense variant T/C;G snv 0.810 1.000 2 2015 2016
melanoma
CUI: C0025202
Disease: melanoma
515 0.763 0.240 3 41224645 missense variant T/C;G snv 0.700 1.000 7 1997 2004
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.763 0.240 3 41224645 missense variant T/C;G snv 0.700 1.000 1 2016 2016
Adenocarcinoma of prostate
CUI: C0007112
Disease: Adenocarcinoma of prostate
108 0.763 0.240 3 41224645 missense variant T/C;G snv 0.700 1.000 1 2016 2016
Adrenocortical carcinoma
CUI: C0206686
Disease: Adrenocortical carcinoma
46 0.763 0.240 3 41224645 missense variant T/C;G snv 0.700 1.000 1 2016 2016
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.763 0.240 3 41224645 missense variant T/C;G snv 0.700 1.000 1 2014 2014
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.763 0.240 3 41224645 missense variant T/C;G snv 0.700 1.000 1 2016 2016
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.763 0.240 3 41224645 missense variant T/C;G snv 0.700 1.000 1 2016 2016
Malignant Uterine Corpus Neoplasm
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
152 0.763 0.240 3 41224645 missense variant T/C;G snv 0.700 1.000 1 2016 2016
Transitional cell carcinoma of bladder
158 0.763 0.240 3 41224645 missense variant T/C;G snv 0.700 1.000 1 2016 2016
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.763 0.240 3 41224645 missense variant T/C;G snv 0.050 1.000 5 1999 2019
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
204 0.763 0.240 3 41224645 missense variant T/C;G snv 0.010 1 2019 2019