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: rs75326924
rs75326924
CD36
4 0.882 0.120 7 80656687 missense variant C/T snv 1.1E-03 1.0E-04 0.700 1.000 9 1995 2015
dbSNP: rs61749397
rs61749397
VWF
9 0.807 0.080 12 6019472 missense variant C/G;T snv 4.0E-06 0.020 1.000 2 2013 2017
dbSNP: rs121909750
rs121909750
GP1BB ; SEPTIN5 ; SEPT5-GP1BB
2 1.000 0.080 22 19724181 missense variant A/G;T snv 4.2E-04 0.010 1.000 1 2001 2001
dbSNP: rs5030764
rs5030764
GP9
5 0.882 0.080 3 129061921 missense variant A/G snv 4.8E-04 7.4E-04 0.010 1.000 1 2016 2016
dbSNP: rs757006129
rs757006129
CHRNE ; GP1BA
3 1.000 0.160 17 4933521 missense variant G/A snv 2.4E-05 1.4E-05 0.010 1.000 1 2015 2015