Source: UNIPROT

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: rs1064794292
rs1064794292
CDKN2A
0.882 0.200 9 21974760 missense variant C/T snv
CUI: C0025202
Disease: melanoma
melanoma 		0.710 1.000 0 2009 2009
dbSNP: rs1064794292
rs1064794292
CDKN2A
0.882 0.200 9 21974760 missense variant C/T snv
CUI: C0030297
Disease: Pancreatic Neoplasm
Pancreatic Neoplasm 		0.700 0