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: rs1046205
rs1046205
1 13 113097743 3 prime UTR variant A/T snv 0.22 0.700 1.000 1 2019 2019
dbSNP: rs1063856
rs1063856
VWF
14 0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 0.700 1.000 1 2013 2013
dbSNP: rs1063857
rs1063857
VWF
4 12 6044348 synonymous variant A/G snv 0.31 0.40 0.700 1.000 1 2013 2013
dbSNP: rs10761784
rs10761784
1 10 63548990 intron variant A/T snv 0.43 0.700 1.000 1 2019 2019
dbSNP: rs113773825
rs113773825
1 16 47003958 upstream gene variant A/T snv 1.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs1149606
rs1149606
1 11 76779014 upstream gene variant G/A snv 0.13 0.700 1.000 1 2019 2019
dbSNP: rs1149616
rs1149616
1 11 76787325 intron variant C/T snv 0.18 0.700 1.000 1 2019 2019
dbSNP: rs117989138
rs117989138
1 13 113043357 non coding transcript exon variant G/A snv 1.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs11907011
rs11907011
1 20 35179967 intron variant C/T snv 8.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs12477385
rs12477385
2 2 165288340 intron variant G/T snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs1260326
rs1260326
81 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.700 1.000 1 2019 2019
dbSNP: rs1755685
rs1755685
2 13 113102878 upstream gene variant C/A snv 0.14 0.700 1.000 1 2019 2019
dbSNP: rs1800961
rs1800961
21 0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs2480952
rs2480952
1 13 113098925 3 prime UTR variant T/C snv 0.23 0.700 1.000 1 2019 2019
dbSNP: rs35866503
rs35866503
1 7 73591446 downstream gene variant C/T snv 0.15 0.700 1.000 1 2019 2019
dbSNP: rs36086577
rs36086577
1 13 113074184 intron variant C/A snv 0.11 0.700 1.000 1 2019 2019
dbSNP: rs474671
rs474671
F10
1 13 113121904 upstream gene variant T/C snv 0.15 0.700 1.000 1 2017 2017
dbSNP: rs498475
rs498475
1 7 28216621 intron variant G/A snv 0.49 0.700 1.000 1 2019 2019
dbSNP: rs56317999
rs56317999
1 20 36757832 intron variant G/A snv 2.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs569557
rs569557
F7
1 13 113115603 intron variant G/A snv 0.12 0.700 1.000 1 2019 2019
dbSNP: rs6083120
rs6083120
1 20 23415361 intron variant C/T snv 8.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs6119569
rs6119569
1 20 35084568 intron variant G/A snv 1.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs6532796
rs6532796
2 1.000 0.040 4 99121091 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs687289
rs687289
ABO
15 1.000 0.120 9 133261703 intron variant A/G snv 0.700 1.000 1 2013 2013
dbSNP: rs71446935
rs71446935
1 13 113080062 intron variant A/G snv 0.700 1.000 1 2019 2019