MEN1, menin 1, 4221

N. diseases: 364; N. variants: 213
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1555166368
rs1555166368
0.851 0.120 11 64809738 frameshift variant GA/- del
CUI: C0021670
Disease: insulinoma
insulinoma
Digestive System Diseases; Neoplasms; Endocrine System Diseases 0.700 0
dbSNP: rs2959656
rs2959656
0.851 0.160 11 64804546 missense variant T/C snv 0.94 0.90
CUI: C0021670
Disease: insulinoma
insulinoma
Digestive System Diseases; Neoplasms; Endocrine System Diseases 0.020 1.000 2 1998 2008