rs28931588, 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 0.701 0.200 3 41224606 missense variant G/A;C;T snv 0.820 1.000 5 1999 2009
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.701 0.200 3 41224606 missense variant G/A;C;T snv 0.800 1.000 1 2016 2016
Craniopharyngioma
CUI: C0010276
Disease: Craniopharyngioma
7 0.701 0.200 3 41224606 missense variant G/A;C;T snv 0.710 1.000 2 2009 2014
Medulloblastoma
CUI: C0025149
Disease: Medulloblastoma
115 0.701 0.200 3 41224606 missense variant G/A;C;T snv 0.700 1.000 2 2014 2016
melanoma
CUI: C0025202
Disease: melanoma
515 0.701 0.200 3 41224606 missense variant G/A;C;T snv 0.700 1.000 2 2009 2014
Adenocarcinoma of prostate
CUI: C0007112
Disease: Adenocarcinoma of prostate
108 0.701 0.200 3 41224606 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.701 0.200 3 41224606 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Endometrial Neoplasms
CUI: C0014170
Disease: Endometrial Neoplasms
32 0.701 0.200 3 41224606 missense variant G/A;C;T snv 0.700 1.000 1 2014 2014
Gastric Adenocarcinoma
CUI: C0278701
Disease: Gastric Adenocarcinoma
235 0.701 0.200 3 41224606 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 0.701 0.200 3 41224606 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
329 0.701 0.200 3 41224606 missense variant G/A;C;T snv 0.700 1.000 1 2014 2014
Transitional cell carcinoma of bladder
CUI: C0279680
Disease: Transitional cell carcinoma of bladder
158 0.701 0.200 3 41224606 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Uterine Cervical Neoplasm
CUI: C0007873
Disease: Uterine Cervical Neoplasm
72 0.701 0.200 3 41224606 missense variant G/A;C;T snv 0.700 1.000 1 2016 2016
Hepatoblastoma
CUI: C0206624
Disease: Hepatoblastoma
22 0.701 0.200 3 41224606 missense variant G/A;C;T snv 0.700 0
Adult Craniopharyngioma
CUI: C0278875
Disease: Adult Craniopharyngioma
6 0.701 0.200 3 41224606 missense variant G/A;C;T snv 0.010 1.000 1 2009 2009
Childhood Craniopharyngioma
CUI: C0278652
Disease: Childhood Craniopharyngioma
6 0.701 0.200 3 41224606 missense variant G/A;C;T snv 0.010 1.000 1 2009 2009
Pilomatrix carcinoma of skin
CUI: C0585475
Disease: Pilomatrix carcinoma of skin
3 0.701 0.200 3 41224606 missense variant G/A;C;T snv 0.010 1.000 1 2009 2009