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: rs137852609
rs137852609
ITGB2
2 0.925 0.080 21 44889376 missense variant G/A snv 1.6E-05 1.4E-05 0.700 0
dbSNP: rs137852610
rs137852610
ITGB2
2 0.925 0.080 21 44901646 missense variant T/C;G snv 4.0E-06 0.700 0
dbSNP: rs137852611
rs137852611
ITGB2
2 0.925 0.080 21 44903418 missense variant A/G snv 0.700 0
dbSNP: rs137852612
rs137852612
ITGB2
2 0.925 0.080 21 44901728 missense variant C/T snv 0.700 0
dbSNP: rs137852613
rs137852613
ITGB2
2 0.925 0.080 21 44895002 missense variant T/C snv 0.700 0
dbSNP: rs137852614
rs137852614
ITGB2
2 0.925 0.080 21 44901700 missense variant G/A snv 1.6E-05 2.1E-05 0.700 0
dbSNP: rs137852615
rs137852615
ITGB2
2 0.925 0.080 21 44903482 missense variant C/A;T snv 8.0E-06 0.700 0
dbSNP: rs137852616
rs137852616
ITGB2
2 0.925 0.080 21 44900367 missense variant C/T snv 4.0E-05 2.8E-05 0.700 0
dbSNP: rs137852617
rs137852617
ITGB2
2 0.925 0.080 21 44903452 missense variant A/G snv 0.700 0
dbSNP: rs137852618
rs137852618
ITGB2
2 0.925 0.080 21 44900400 missense variant C/T snv 1.6E-05 6.3E-05 0.700 0
dbSNP: rs201752283
rs201752283
ITGB2
2 0.925 0.080 21 44900319 splice donor variant C/A;T snv 2.0E-05 0.700 0
dbSNP: rs387906411
rs387906411
ITGB2 ; LOC107987303
1 1.000 21 44910781 start lost A/T snv 7.0E-06 0.700 0