Gene: MAP2K2 ×
Source: CLINVAR ×
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: rs121434497
rs121434497
MAP2K2
2 0.925 0.160 19 4117552 missense variant A/C;T snv 0.800 1.000 0 2006 2010
dbSNP: rs121434498
rs121434498
MAP2K2
6 0.807 0.280 19 4117553 missense variant A/C;G;T snv 0.800 1.000 0 2006 2010
dbSNP: rs121434499
rs121434499
MAP2K2
2 0.925 0.160 19 4110559 missense variant A/G snv 0.800 1.000 0 2006 2010
dbSNP: rs267607230
rs267607230
MAP2K2
2 0.925 0.160 19 4110576 missense variant G/A;C;T snv 0.800 1.000 0 2006 2010
dbSNP: rs1057519806
rs1057519806
MAP2K2
3 0.882 0.200 19 4110583 missense variant T/C snv 0.700 0
dbSNP: rs1135401787
rs1135401787
MAP2K2
1 1.000 19 4117531 missense variant A/C;G snv 4.0E-06 0.700 0
dbSNP: rs387906800
rs387906800
MAP2K2
1 1.000 19 4110564 missense variant C/T snv 0.700 0