rs121913403, CTNNB1

N. diseases: 23
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 0.683 0.240 3 41224622 missense variant C/A;G;T snv 0.700 1.000 7 1997 2004
Pilomatrixoma
CUI: C0206711
Disease: Pilomatrixoma
14 0.683 0.240 3 41224622 missense variant C/A;G;T snv 0.810 1.000 7 1999 2017
Malignant neoplasm of ovary
CUI: C1140680
Disease: Malignant neoplasm of ovary
315 0.683 0.240 3 41224622 missense variant C/A;G;T snv 0.700 1.000 3 2008 2013
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.683 0.240 3 41224622 missense variant C/A;G;T snv 0.700 1.000 2 2014 2016
Adenocarcinoma of prostate
CUI: C0007112
Disease: Adenocarcinoma of prostate
108 0.683 0.240 3 41224622 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Adult Craniopharyngioma
CUI: C0278875
Disease: Adult Craniopharyngioma
6 0.683 0.240 3 41224622 missense variant C/A;G;T snv 0.010 1.000 1 2009 2009
Carcinoma
CUI: C0007097
Disease: Carcinoma
103 0.683 0.240 3 41224622 missense variant C/A;G;T snv 0.010 1.000 1 1998 1998
Carcinoma, Basal Cell
CUI: C4721806
Disease: Carcinoma, Basal Cell
91 0.683 0.240 3 41224622 missense variant C/A;G;T snv 0.010 1.000 1 2009 2009
Childhood Craniopharyngioma
CUI: C0278652
Disease: Childhood Craniopharyngioma
6 0.683 0.240 3 41224622 missense variant C/A;G;T snv 0.010 1.000 1 2009 2009
Craniopharyngioma
CUI: C0010276
Disease: Craniopharyngioma
7 0.683 0.240 3 41224622 missense variant C/A;G;T snv 0.010 1.000 1 2009 2009
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.683 0.240 3 41224622 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
235 0.683 0.240 3 41224622 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.683 0.240 3 41224622 missense variant C/A;G;T snv 0.800 1.000 1 2016 2016
Malignant Uterine Corpus Neoplasm
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
152 0.683 0.240 3 41224622 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Medulloblastoma
CUI: C0025149
Disease: Medulloblastoma
115 0.683 0.240 3 41224622 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Neoplasm Metastasis
CUI: C0027627
Disease: Neoplasm Metastasis
327 0.683 0.240 3 41224622 missense variant C/A;G;T snv 0.010 1.000 1 2003 2003
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.683 0.240 3 41224622 missense variant C/A;G;T snv 0.010 1.000 1 1998 1998
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.683 0.240 3 41224622 missense variant C/A;G;T snv 0.700 1.000 1 2014 2014
Pilomatrix carcinoma of skin
CUI: C0585475
Disease: Pilomatrix carcinoma of skin
3 0.683 0.240 3 41224622 missense variant C/A;G;T snv 0.010 1.000 1 2009 2009
Stomach Neoplasms
CUI: C0038356
Disease: Stomach Neoplasms
55 0.683 0.240 3 41224622 missense variant C/A;G;T snv 0.700 1.000 1 2014 2014
Supratentorial Embryonal Tumor, Not Otherwise Specified
4 0.683 0.240 3 41224622 missense variant C/A;G;T snv 0.010 1.000 1 2001 2001
Transitional cell carcinoma of bladder
158 0.683 0.240 3 41224622 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
Uterine Cervical Neoplasm
CUI: C0007873
Disease: Uterine Cervical Neoplasm
72 0.683 0.240 3 41224622 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016