rs28931589, CTNNB1

N. diseases: 17
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.
Pilomatrixoma
CUI: C0206711
Disease: Pilomatrixoma
14 0.695 0.240 3 41224613 missense variant G/A;C;T snv 0.800 1.000 6 1999 2017
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.695 0.240 3 41224613 missense variant G/A;C;T snv 0.710 1.000 3 2014 2016
Craniopharyngioma
CUI: C0010276
Disease: Craniopharyngioma
7 0.695 0.240 3 41224613 missense variant G/A;C;T snv 0.710 1.000 2 2009 2014
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 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
46 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
248 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
235 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
152 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
115 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
515 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
757 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
348 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
22 0.695 0.240 3 41224613 missense variant G/A;C;T snv 0.700 0
Adult Craniopharyngioma
CUI: C0278875
Disease: Adult Craniopharyngioma
6 0.695 0.240 3 41224613 missense variant G/A;C;T snv 0.010 1.000 1 2009 2009
Childhood Craniopharyngioma
CUI: C0278652
Disease: Childhood Craniopharyngioma
6 0.695 0.240 3 41224613 missense variant G/A;C;T snv 0.010 1.000 1 2009 2009
Microcystic stromal tumor
CUI: C3838965
Disease: Microcystic stromal tumor
2 0.695 0.240 3 41224613 missense variant G/A;C;T snv 0.010 1.000 1 2015 2015
Supratentorial Embryonal Tumor, Not Otherwise Specified
4 0.695 0.240 3 41224613 missense variant G/A;C;T snv 0.010 1.000 1 2001 2001