rs121913403, CTNNB1

N. diseases: 10
Source: BEFREE ×
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
2 0.683 0.240 3 41224622 missense variant C/A;G;T snv 0.810 1.000 1 1999 2017
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
90 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
65 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
6 0.683 0.240 3 41224622 missense variant C/A;G;T snv 0.010 1.000 1 2009 2009
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
1571 0.683 0.240 3 41224622 missense variant C/A;G;T snv 0.010 1.000 1 1998 1998
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
Supratentorial Embryonal Tumor, Not Otherwise Specified
CUI: C1336538
Disease: 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