rs1057519708, KIT

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.
melanoma
CUI: C0025202
Disease: melanoma
515 1.000 0.040 4 54728096 missense variant T/A;G snv 0.700 1.000 3 2011 2014
Gastrointestinal Stromal Tumors
CUI: C0238198
Disease: Gastrointestinal Stromal Tumors
154 1.000 0.040 4 54728096 missense variant T/A;G snv 0.700 1.000 2 2007 2011