rs121913396, CTNNB1

N. diseases: 13
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 0.732 0.200 3 41224607 missense variant A/C;G;T snv 0.800 1.000 3 2013 2017
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.732 0.200 3 41224607 missense variant A/C;G;T snv 0.800 1.000 1 2016 2016
Adenocarcinoma of prostate
CUI: C0007112
Disease: Adenocarcinoma of prostate
108 0.732 0.200 3 41224607 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.732 0.200 3 41224607 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Endometrial Neoplasms
CUI: C0014170
Disease: Endometrial Neoplasms
32 0.732 0.200 3 41224607 missense variant A/C;G;T snv 0.700 1.000 1 2014 2014
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
235 0.732 0.200 3 41224607 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Malignant Uterine Corpus Neoplasm
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
152 0.732 0.200 3 41224607 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Medulloblastoma
CUI: C0025149
Disease: Medulloblastoma
115 0.732 0.200 3 41224607 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
melanoma
CUI: C0025202
Disease: melanoma
515 0.732 0.200 3 41224607 missense variant A/C;G;T snv 0.700 1.000 1 2014 2014
Transitional cell carcinoma of bladder
CUI: C0279680
Disease: Transitional cell carcinoma of bladder
158 0.732 0.200 3 41224607 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Uterine Cervical Neoplasm
CUI: C0007873
Disease: Uterine Cervical Neoplasm
72 0.732 0.200 3 41224607 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.732 0.200 3 41224607 missense variant A/C;G;T snv 0.010 1.000 1 2012 2012
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.732 0.200 3 41224607 missense variant A/C;G;T snv 0.010 1.000 1 2012 2012