Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs879254764
LDLR
0.827 0.360 19 11110752 frameshift variant G/- delins 7
rs121908065
CHRNE ; GP1BA
0.851 0.080 17 4933119 missense variant C/T snv 5
rs5030764
GP9
0.882 0.080 3 129061921 missense variant A/G snv 4.8E-04 7.4E-04 5
rs121908063
GP1BA ; CHRNE
0.882 0.080 17 4932821 missense variant C/T snv 3
rs121918037
GP9
0.882 0.080 3 129061951 missense variant T/C;G snv 4.0E-06 3
rs1394634674
CHRNE ; GP1BA
0.925 0.080 17 4933277 missense variant T/A snv 4.0E-06 2
rs121918036
GP9
0.925 0.080 3 129061849 missense variant A/G snv 2
rs121918038
GP9
0.925 0.080 3 129061759 missense variant T/C snv 2
rs28933377
GP9
0.925 0.080 3 129061906 missense variant T/C snv 6.9E-05 8.4E-05 2
rs28933378
GP9
0.925 0.080 3 129061809 missense variant T/C snv 7.8E-05 7.0E-06 2
rs121909750
SEPTIN5 ; SEPT5-GP1BB ; GP1BB
1.000 0.080 22 19724181 missense variant A/G;T snv 4.2E-04 2
rs753947399
CHRNE ; GP1BA
1.000 0.080 17 4933271 missense variant T/G snv 4.0E-06 1
rs1555549041
GP1BA ; CHRNE
1.000 0.080 17 4932707 frameshift variant A/- delins 1
rs771048666
GP1BA ; CHRNE
1.000 0.080 17 4933038 missense variant T/C snv 1.2E-04 1.3E-04 1
rs781541857
GP1BA ; CHRNE
1.000 0.080 17 4932845 missense variant T/C snv 1
rs121909751
GP1BB ; SEPT5-GP1BB
1.000 0.080 22 19724240 missense variant G/C snv 1
rs587783648
GP1BB ; SEPT5-GP1BB ; SEPTIN5
1.000 0.080 22 19724183 missense variant C/T snv 7.1E-06 1
rs776621159
GP5
1.000 0.080 3 194398266 missense variant A/G snv 3.5E-05 3.5E-05 1
rs181991348
PAX5
1.000 0.080 9 36840636 missense variant C/G snv 1.2E-05 1
rs759081917
PRB1 ; PRB2
1.000 0.080 12 11393857 missense variant G/A;C snv 4.1E-06 1
rs1442458912
PRB2 ; PRB1
1.000 0.080 12 11393944 missense variant T/C snv 4.0E-06 1
rs1012488531
VWF
1.000 0.080 12 6121263 missense variant T/C;G snv 4.0E-06 1
rs1305880207
VWF
1.000 0.080 12 6110550 missense variant T/C snv 1.2E-05 7.0E-06 1