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: rs1010184002
rs1010184002
60 0.689 0.400 6 42978878 stop gained C/T snv 7.0E-06 0.700 0
dbSNP: rs1014959895
rs1014959895
16 0.763 0.360 16 68329105 stop gained G/C;T snv 4.0E-06; 1.6E-05 0.700 0
dbSNP: rs1057518848
rs1057518848
15 0.827 0.240 18 55229003 frameshift variant -/ATTG delins 0.700 0
dbSNP: rs1057518934
rs1057518934
8 0.851 0.240 15 28211095 frameshift variant G/- delins 0.700 0
dbSNP: rs1057518950
rs1057518950
TPO
7 0.851 0.280 2 1484815 missense variant C/T snv 0.700 0
dbSNP: rs1131692231
rs1131692231
13 0.827 0.280 5 157294834 missense variant C/T snv 0.700 0
dbSNP: rs1131692272
rs1131692272
9 0.851 0.240 2 100006808 missense variant C/T snv 0.700 0
dbSNP: rs1135401761
rs1135401761
2 0.925 0.200 1 27548302 stop gained G/A;C snv 0.700 0
dbSNP: rs1223073957
rs1223073957
12 0.827 0.240 19 49835897 frameshift variant C/- delins 1.2E-05 1.4E-05 0.700 0
dbSNP: rs122445099
rs122445099
6 0.827 0.400 X 77520832 stop gained G/A snv 0.700 0
dbSNP: rs1251713297
rs1251713297
15 0.776 0.360 16 68355785 stop gained C/A snv 8.1E-06 0.700 0
dbSNP: rs1325394060
rs1325394060
9 0.851 0.320 X 53534144 missense variant C/G;T snv 9.5E-06 0.700 0
dbSNP: rs1553655558
rs1553655558
43 0.752 0.360 2 229830831 frameshift variant A/- delins 0.700 0
dbSNP: rs1554691658
rs1554691658
11 0.807 0.240 9 95459653 frameshift variant C/GGGTCCACAACATCT delins 0.700 0
dbSNP: rs1555103652
rs1555103652
11 0.882 0.240 12 13569973 missense variant A/C snv 0.700 0
dbSNP: rs1555321402
rs1555321402
3 0.925 0.240 14 28768345 frameshift variant T/- delins 0.700 0
dbSNP: rs1555954284
rs1555954284
24 0.752 0.360 X 41346607 missense variant C/T snv 0.700 0
dbSNP: rs1556024875
rs1556024875
4 0.882 0.160 X 123634002 missense variant G/A snv 0.700 0
dbSNP: rs1556910184
rs1556910184
4 0.882 0.240 X 53534615 missense variant C/G snv 0.700 0
dbSNP: rs1556913258
rs1556913258
7 0.851 0.280 X 53536580 missense variant G/C snv 0.700 0
dbSNP: rs1556913268
rs1556913268
6 0.851 0.240 X 53536600 missense variant T/A snv 0.700 0
dbSNP: rs1556914274
rs1556914274
13 0.790 0.440 X 53537626 missense variant G/A snv 0.700 0
dbSNP: rs1556978515
rs1556978515
7 0.851 0.280 X 53591113 missense variant T/C snv 0.700 0
dbSNP: rs1557006903
rs1557006903
5 0.851 0.280 X 53615815 missense variant C/T snv 0.700 0
dbSNP: rs1557024919
rs1557024919
7 0.925 0.240 X 53634235 splice donor variant C/G snv 0.700 0