rs747518441, SDHB

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.
Gastrointestinal Stromal Tumors
CUI: C0238198
Disease: Gastrointestinal Stromal Tumors
154 1.000 0.080 1 17022723 missense variant C/A;T snv 4.0E-06; 8.0E-06 0.700 0
Hamartoma Syndrome, Multiple
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
139 1.000 0.080 1 17022723 missense variant C/A;T snv 4.0E-06; 8.0E-06 0.700 0