Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1063856
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31
CUI: C1167912
Disease: Coagulation factor measurement
Coagulation factor measurement
0.700 1.000 1 2013 2013
dbSNP: rs1063857
rs1063857
VWF
12 6044348 synonymous variant A/G snv 0.31 0.40
CUI: C1167912
Disease: Coagulation factor measurement
Coagulation factor measurement
0.700 1.000 1 2013 2013
dbSNP: rs10665
rs10665
13 113098517 3 prime UTR variant A/G snv 0.12
CUI: C1167912
Disease: Coagulation factor measurement
Coagulation factor measurement
0.700 1.000 1 2013 2013
dbSNP: rs10922162
rs10922162
1 197101646 synonymous variant C/T snv 0.26 0.16
CUI: C1167912
Disease: Coagulation factor measurement
Coagulation factor measurement
0.700 1.000 1 2013 2013
dbSNP: rs10982156
rs10982156
9 114325784 intron variant T/A snv 7.0E-02
CUI: C1167912
Disease: Coagulation factor measurement
Coagulation factor measurement
0.700 1.000 1 2013 2013
dbSNP: rs11243081
rs11243081
6 6337273 intergenic variant C/T snv 0.23
CUI: C1167912
Disease: Coagulation factor measurement
Coagulation factor measurement
0.700 1.000 1 2013 2013
dbSNP: rs12116643
rs12116643
1 197004053 intron variant T/C snv 0.19
CUI: C1167912
Disease: Coagulation factor measurement
Coagulation factor measurement
0.700 1.000 1 2013 2013
dbSNP: rs1318606
rs1318606
6 6331703 intergenic variant T/C snv 0.38
CUI: C1167912
Disease: Coagulation factor measurement
Coagulation factor measurement
0.700 1.000 1 2013 2013
dbSNP: rs1410996
rs1410996
CFH
0.807 0.240 1 196727803 intron variant G/A snv 0.46
CUI: C1167912
Disease: Coagulation factor measurement
Coagulation factor measurement
0.700 1.000 1 2013 2013
dbSNP: rs17142067
rs17142067
6 6341054 intergenic variant A/C;G snv 0.23
CUI: C1167912
Disease: Coagulation factor measurement
Coagulation factor measurement
0.700 1.000 1 2013 2013
dbSNP: rs2022309
rs2022309
1 94586920 intron variant G/T snv 0.23
CUI: C1167912
Disease: Coagulation factor measurement
Coagulation factor measurement
0.700 1.000 1 2013 2013
dbSNP: rs2181540
rs2181540
13 113098850 3 prime UTR variant T/C snv 0.15
CUI: C1167912
Disease: Coagulation factor measurement
Coagulation factor measurement
0.700 1.000 1 2013 2013
dbSNP: rs3024321
rs3024321
6 6317893 intron variant A/G snv 0.29
CUI: C1167912
Disease: Coagulation factor measurement
Coagulation factor measurement
0.700 1.000 1 2013 2013
dbSNP: rs3211770
rs3211770
F10
13 113139535 intron variant G/A snv 0.11
CUI: C1167912
Disease: Coagulation factor measurement
Coagulation factor measurement
0.700 1.000 1 2013 2013
dbSNP: rs379440
rs379440
5 112357674 intron variant T/C snv 3.5E-02
CUI: C1167912
Disease: Coagulation factor measurement
Coagulation factor measurement
0.700 1.000 1 2011 2011
dbSNP: rs4686760
rs4686760
3 184796825 intergenic variant G/A;C snv
CUI: C1167912
Disease: Coagulation factor measurement
Coagulation factor measurement
0.700 1.000 1 2011 2011
dbSNP: rs4915559
rs4915559
1.000 0.040 1 196917640 intron variant T/A;C snv
CUI: C1167912
Disease: Coagulation factor measurement
Coagulation factor measurement
0.700 1.000 1 2013 2013
dbSNP: rs555212
rs555212
13 113102226 upstream gene variant A/G snv 0.79
CUI: C1167912
Disease: Coagulation factor measurement
Coagulation factor measurement
0.700 1.000 1 2013 2013
dbSNP: rs5985
rs5985
0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05
CUI: C1167912
Disease: Coagulation factor measurement
Coagulation factor measurement
0.700 1.000 1 2013 2013
dbSNP: rs6041
rs6041
F7
13 113118393 intron variant G/A snv 0.13 0.12
CUI: C1167912
Disease: Coagulation factor measurement
Coagulation factor measurement
0.700 1.000 1 2013 2013
dbSNP: rs6708166
rs6708166
LBH
2 30303914 intron variant G/A snv 0.32
CUI: C1167912
Disease: Coagulation factor measurement
Coagulation factor measurement
0.700 1.000 1 2011 2011
dbSNP: rs687289
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv
CUI: C1167912
Disease: Coagulation factor measurement
Coagulation factor measurement
0.700 1.000 1 2013 2013
dbSNP: rs7410943
rs7410943
1 197185891 intron variant A/G snv 0.44
CUI: C1167912
Disease: Coagulation factor measurement
Coagulation factor measurement
0.700 1.000 1 2013 2013
dbSNP: rs8176704
rs8176704
ABO
0.925 0.080 9 133260148 intron variant G/A snv
CUI: C1167912
Disease: Coagulation factor measurement
Coagulation factor measurement
0.700 1.000 1 2013 2013
dbSNP: rs8176749
rs8176749
ABO
1.000 0.040 9 133255801 synonymous variant C/T snv 0.12 0.11
CUI: C1167912
Disease: Coagulation factor measurement
Coagulation factor measurement
0.700 1.000 1 2013 2013