Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 16
rs3811381
CR1
0.763 0.240 1 207616743 missense variant C/A;G snv 8.0E-06; 0.24 11
rs2274567
CR1
0.776 0.400 1 207580276 missense variant A/G snv 0.25 0.21 10
rs368927897
JAK2 ; INSL6
0.790 0.240 9 5072541 missense variant G/A;T snv 2.8E-05; 6.4E-05 9
rs397514767
CD59
0.807 0.240 11 33710247 missense variant C/T snv 4.0E-06 7
rs1445335859
PIGA
0.851 0.240 X 15331662 missense variant T/C snv 9.4E-06 5
rs137853315
FLNA
0.882 0.200 X 154368081 missense variant G/A snv 3
rs34422225
PIGA
0.925 0.040 X 15331876 missense variant G/A snv 3.0E-02 3.1E-02 2
rs782549964
FLNA
1.000 0.040 X 154353704 missense variant C/T snv 4.5E-05 5.6E-05 1