rs28931589, CTNNB1

N. diseases: 13
Source: INFERRED ×
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.
Pilomatrixoma
CUI: C0206711
Disease: Pilomatrixoma
0.695 0.240 3 41224613 missense variant G/A;C;T snv 0.800 1.000 0 1999 2017
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
0.695 0.240 3 41224613 missense variant G/A;C;T snv 0.710 1.000 2 2014 2016
Craniopharyngioma
CUI: C0010276
Disease: Craniopharyngioma
0.695 0.240 3 41224613 missense variant G/A;C;T snv 0.710 1.000 1 2009 2014
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
0.695 0.240 3 41224613 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Adrenocortical carcinoma
CUI: C0206686
Disease: Adrenocortical carcinoma
0.695 0.240 3 41224613 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
0.695 0.240 3 41224613 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
0.695 0.240 3 41224613 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Malignant Uterine Corpus Neoplasm
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
0.695 0.240 3 41224613 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Medulloblastoma
CUI: C0025149
Disease: Medulloblastoma
0.695 0.240 3 41224613 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
melanoma
CUI: C0025202
Disease: melanoma
0.695 0.240 3 41224613 missense variant G/A;C;T snv 0.700 1.000 1 2014 2014
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
0.695 0.240 3 41224613 missense variant G/A;C;T snv 0.700 1.000 1 2014 2014
Squamous cell carcinoma of the head and neck
CUI: C1168401
Disease: Squamous cell carcinoma of the head and neck
0.695 0.240 3 41224613 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Hepatoblastoma
CUI: C0206624
Disease: Hepatoblastoma
0.695 0.240 3 41224613 missense variant G/A;C;T snv 0.700 0