rs41303402, SMO

N. diseases: 2
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.
Carcinoma, Basal Cell
CUI: C4721806
Disease: Carcinoma, Basal Cell
91 1.000 0.040 7 129203437 missense variant G/A;T snv 1.0E-04; 5.7E-06 0.010 1.000 1 2016 2016
Experimental Organism Basal Cell Carcinoma
63 1.000 0.040 7 129203437 missense variant G/A;T snv 1.0E-04; 5.7E-06 0.010 1.000 1 2016 2016