Source: ALL

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: rs2518564
rs2518564
AIM2
1 159092646 intron variant G/A snv 0.60
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.800 1.000 3 2011 2019
dbSNP: rs1103577
rs1103577
AIM2
1 159130525 intron variant T/C snv 0.45
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs11265142
rs11265142
AIM2
1 159130118 intron variant A/G snv 8.4E-02
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1894043
rs1894043
AIM2
1 159099421 intron variant T/C snv 0.60
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs1894044
rs1894044
AIM2
1 159118544 intron variant G/A;C snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs2276405
rs2276405
AIM2
1.000 0.040 1 159073406 stop gained C/A;T snv 8.0E-06; 1.5E-02
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2015 2015
dbSNP: rs2518569
rs2518569
AIM2
1 159125785 intron variant T/G snv 0.80
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2518570
rs2518570
AIM2
1 159127112 intron variant C/G snv 0.70
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs2814764
rs2814764
AIM2
1 159094778 intron variant A/T snv 0.71
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs2852720
rs2852720
AIM2
1 159090770 intron variant T/C snv 0.79
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs2852727
rs2852727
AIM2
1 159117196 intron variant G/A snv 0.49
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs855866
rs855866
AIM2
1 159082930 intron variant A/G snv 0.61
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs855867
rs855867
AIM2
1 159083057 intron variant G/A;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs855871
rs855871
AIM2
1 159074861 intron variant G/A;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs855873
rs855873
AIM2
1.000 0.200 1 159077922 intron variant A/G snv 0.84
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.010 1.000 1 2015 2015