Source: ALL
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: rs137852908
rs137852908
ITGA2B
1 1.000 0.080 17 44383630 missense variant C/T snv 0.810 0.952 21 1994 2010
dbSNP: rs137852907
rs137852907
ITGA2B
1 1.000 0.080 17 44384567 missense variant C/T snv 0.810 1.000 20 1994 2010
dbSNP: rs137852911
rs137852911
ITGA2B
1 1.000 0.080 17 44385193 missense variant A/C;G snv 4.0E-06 0.810 1.000 20 1994 2010
dbSNP: rs121918447
rs121918447
ITGB3 ; THCAT158
1 1.000 0.080 17 47310169 missense variant T/C snv 0.810 1.000 19 1990 2017
dbSNP: rs121918449
rs121918449
ITGB3
1 1.000 0.080 17 47291027 missense variant G/A snv 0.810 1.000 19 1990 2017
dbSNP: rs137852910
rs137852910
ITGA2B
1 1.000 0.080 17 44383640 missense variant C/T snv 8.8E-06 0.800 1.000 20 1994 2010
dbSNP: rs121918444
rs121918444
ITGB3
1 1.000 0.080 17 47286364 missense variant G/A snv 7.0E-06 0.800 1.000 19 1990 2017
dbSNP: rs121918445
rs121918445
ITGB3
1 1.000 0.080 17 47284514 missense variant G/T snv 0.800 1.000 19 1990 2017
dbSNP: rs121918446
rs121918446
ITGB3
1 1.000 0.080 17 47286363 missense variant C/T snv 1.2E-05 7.0E-06 0.800 1.000 19 1990 2017
dbSNP: rs121918452
rs121918452
ITGB3
1 1.000 0.080 17 47284509 missense variant T/G snv 2.0E-05 0.800 1.000 19 1990 2017
dbSNP: rs79775494
rs79775494
ITGB3
1 1.000 0.080 17 47287128 missense variant A/T snv 4.0E-06 7.0E-06 0.800 1.000 19 1990 2017
dbSNP: rs74475415
rs74475415
ITGA2B
1 1.000 0.080 17 44376323 missense variant T/G snv 8.0E-06 0.800 1.000 2 1998 2012
dbSNP: rs76811038
rs76811038
ITGA2B
1 1.000 0.080 17 44379780 missense variant A/G snv 6.4E-05 5.6E-05 0.800 0
dbSNP: rs79560904
rs79560904
ITGB3
1 1.000 0.080 17 47286385 missense variant G/A snv 0.800 0
dbSNP: rs80002943
rs80002943
ITGA2B
1 1.000 0.080 17 44374732 missense variant G/A snv 0.800 0
dbSNP: rs75622274
rs75622274
ITGA2B
1 1.000 0.080 17 44381058 missense variant A/C;G snv 4.0E-06 0.700 1.000 20 1994 2010
dbSNP: rs761174160
rs761174160
ITGA2B
1 1.000 0.080 17 44377022 missense variant G/C snv 4.6E-06 0.700 1.000 20 1994 2010
dbSNP: rs763762304
rs763762304
ITGA2B
1 1.000 0.080 17 44377012 missense variant C/G;T snv 4.7E-06; 5.6E-05 0.700 1.000 20 1994 2010
dbSNP: rs766006685
rs766006685
ITGA2B
1 1.000 0.080 17 44383564 missense variant C/T snv 0.700 1.000 20 1994 2010
dbSNP: rs780786843
rs780786843
ITGA2B
1 1.000 0.080 17 44381038 missense variant C/A;G;T snv 4.0E-06; 3.2E-05 0.700 1.000 20 1994 2010
dbSNP: rs879255514
rs879255514
ITGA2B
2 0.925 0.080 17 44372407 missense variant C/T snv 4.0E-06 0.700 1.000 20 1994 2010
dbSNP: rs143146734
rs143146734
ITGB3
1 1.000 0.080 17 47284644 missense variant C/T snv 4.0E-06 0.700 1.000 19 1990 2017
dbSNP: rs144884023
rs144884023
ITGB3
1 1.000 0.080 17 47299430 missense variant G/A snv 1.2E-05 1.4E-05 0.700 1.000 19 1990 2017
dbSNP: rs377162158
rs377162158
ITGB3
1 1.000 0.080 17 47286370 missense variant G/A snv 1.4E-05 0.700 1.000 19 1990 2017
dbSNP: rs74554539
rs74554539
ITGB3
1 1.000 0.080 17 47283379 missense variant G/A snv 0.700 1.000 19 1990 2017