rs1057519805, MAP2K1

N. diseases: 3
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 15 66436839 missense variant T/C snv 0.700 1.000 2 2009 2013
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 1.000 0.040 15 66436839 missense variant T/C snv 0.010 1.000 1 2011 2011
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 1.000 0.040 15 66436839 missense variant T/C snv 0.010 1.000 1 2011 2011