Gene: MEN1 ×
Source: UNIPROT ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1064793167
rs1064793167
MEN1
1 1.000 0.120 11 64808010 missense variant C/T snv 0.700 0
dbSNP: rs1114167469
rs1114167469
MEN1
1 0.925 0.160 11 64806322 missense variant G/A snv 0.700 0
dbSNP: rs1114167493
rs1114167493
MEN1
1 1.000 0.120 11 64807082 missense variant C/T snv 0.700 0
dbSNP: rs1114167494
rs1114167494
MEN1
1 1.000 0.120 11 64808031 missense variant C/A snv 0.700 0
dbSNP: rs1114167495
rs1114167495
MEN1
1 1.000 0.120 11 64806331 missense variant T/C snv 0.700 0
dbSNP: rs1114167515
rs1114167515
MEN1
1 1.000 0.120 11 64809694 missense variant T/C snv 0.700 0
dbSNP: rs1114167528
rs1114167528
MEN1 ; MAP4K2
1 1.000 0.120 11 64805103 missense variant A/T snv 0.800 0
dbSNP: rs863224527
rs863224527
MEN1 ; MAP4K2
1 1.000 0.120 11 64804503 missense variant C/T snv 0.800 0
dbSNP: rs886039415
rs886039415
MEN1
1 1.000 0.120 11 64807667 missense variant A/G snv 0.700 0
dbSNP: rs104894256
rs104894256
MEN1
1 1.000 0.120 11 64810045 missense variant A/C snv 0.800 1.000 28 1997 2017
dbSNP: rs104894259
rs104894259
MEN1 ; MAP4K2
1 1.000 0.120 11 64805078 missense variant A/G;T snv 0.800 1.000 28 1997 2017
dbSNP: rs104894263
rs104894263
MEN1
1 1.000 0.120 11 64809695 missense variant G/C snv 0.810 1.000 28 1997 2017
dbSNP: rs104894264
rs104894264
MEN1 ; MAP4K2
1 1.000 0.120 11 64805132 missense variant C/A;G;T snv 0.800 1.000 28 1997 2017
dbSNP: rs1555164707
rs1555164707
MEN1
1 1.000 0.120 11 64805717 missense variant G/T snv 0.800 1.000 28 1997 2017
dbSNP: rs2071312
rs2071312
MEN1
1 1.000 0.120 11 64806272 missense variant C/G;T snv 0.700 1.000 28 1997 2017
dbSNP: rs794728621
rs794728621
MEN1
1 1.000 0.120 11 64807902 missense variant C/T snv 0.700 1.000 28 1997 2017
dbSNP: rs863224807
rs863224807
MEN1
1 1.000 0.120 11 64805757 missense variant G/A;T snv 0.700 1.000 28 1997 2017
dbSNP: rs1057521110
rs1057521110
MEN1
1 1.000 0.120 11 64807662 missense variant C/T snv 0.700 1.000 20 1997 2005
dbSNP: rs1114167543
rs1114167543
MEN1
1 1.000 0.120 11 64809680 missense variant A/C snv 0.700 1.000 20 1997 2005
dbSNP: rs1387157979
rs1387157979
MEN1 ; MAP4K2
1 1.000 0.120 11 64804537 missense variant G/A snv 4.0E-06 0.700 1.000 20 1997 2005
dbSNP: rs1389398299
rs1389398299
MEN1
1 1.000 0.120 11 64809781 missense variant C/G;T snv 8.0E-06 0.700 1.000 20 1997 2005
dbSNP: rs1555165811
rs1555165811
MEN1
1 1.000 0.120 11 64808008 missense variant C/A;G snv 0.700 1.000 20 1997 2005
dbSNP: rs28931612
rs28931612
MEN1
1 0.925 0.120 11 64810034 stop gained C/A;T snv 0.700 1.000 20 1997 2005
dbSNP: rs387906552
rs387906552
MEN1
1 1.000 0.120 11 64805745 missense variant C/T snv 0.700 1.000 20 1997 2005
dbSNP: rs398124435
rs398124435
MEN1 ; MAP4K2
1 1.000 0.120 11 64805076 missense variant C/A snv 0.800 1.000 20 1997 2012