rs1024708183, MAP2K7

N. diseases: 4
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 0.925 0.040 19 7909761 missense variant A/G snv 0.020 1.000 2 2005 2015
Congenital chromosomal disease
CUI: C0008626
Disease: Congenital chromosomal disease
47 0.925 0.040 19 7909761 missense variant A/G snv 0.010 1.000 1 2018 2018
Metastatic melanoma
CUI: C0278883
Disease: Metastatic melanoma
42 0.925 0.040 19 7909761 missense variant A/G snv 0.010 1.000 1 2016 2016
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.925 0.040 19 7909761 missense variant A/G snv 0.010 1.000 1 2019 2019