Gene: AIM2 ×
Source: INFERRED ×
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: rs2518564
rs2518564
AIM2
1 1 159092646 intron variant G/A snv 0.60 0.800 1.000 3 2011 2019
dbSNP: rs1103577
rs1103577
AIM2
1 1 159130525 intron variant T/C snv 0.45 0.700 1.000 1 2011 2011
dbSNP: rs1894043
rs1894043
AIM2
1 1 159099421 intron variant T/C snv 0.60 0.700 1.000 1 2011 2011
dbSNP: rs1894044
rs1894044
AIM2
1 1 159118544 intron variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs2518570
rs2518570
AIM2
1 1 159127112 intron variant C/G snv 0.70 0.700 1.000 1 2011 2011
dbSNP: rs2814764
rs2814764
AIM2
1 1 159094778 intron variant A/T snv 0.71 0.700 1.000 1 2011 2011
dbSNP: rs2852720
rs2852720
AIM2
1 1 159090770 intron variant T/C snv 0.79 0.700 1.000 1 2011 2011
dbSNP: rs2852727
rs2852727
AIM2
1 1 159117196 intron variant G/A snv 0.49 0.700 1.000 1 2011 2011
dbSNP: rs855866
rs855866
AIM2
1 1 159082930 intron variant A/G snv 0.61 0.700 1.000 1 2011 2011
dbSNP: rs855867
rs855867
AIM2
1 1 159083057 intron variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs855871
rs855871
AIM2
1 1 159074861 intron variant G/A;T snv 0.700 1.000 1 2011 2011