Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1024708183
rs1024708183
MAP2K7
0.925 0.040 19 7909761 missense variant A/G snv
CUI: C0025202
Disease: melanoma
melanoma 		0.020 1.000 2 2005 2015
dbSNP: rs1024708183
rs1024708183
MAP2K7
0.925 0.040 19 7909761 missense variant A/G snv
CUI: C0278883
Disease: Metastatic melanoma
Metastatic melanoma 		0.010 1.000 1 2016 2016
dbSNP: rs1024708183
rs1024708183
MAP2K7
0.925 0.040 19 7909761 missense variant A/G snv
CUI: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease 		0.010 1.000 1 2018 2018
dbSNP: rs1024708183
rs1024708183
MAP2K7
0.925 0.040 19 7909761 missense variant A/G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 2019 2019