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: rs10011025
rs10011025
1 1.000 0.120 4 174733072 intron variant A/C;G snv 0.010 1.000 1 2018 2018
dbSNP: rs10181656
rs10181656
9 0.763 0.360 2 191105153 intron variant G/C snv 0.79 0.010 1.000 1 2008 2008
dbSNP: rs10186193
rs10186193
1 1.000 0.120 2 3550384 synonymous variant T/C snv 0.33 0.41 0.010 1.000 1 2018 2018
dbSNP: rs1020856343
rs1020856343
5 0.851 0.240 5 132393705 missense variant C/T snv 4.0E-06 0.010 1.000 1 2006 2006
dbSNP: rs1022059218
rs1022059218
2 0.925 0.200 2 203936863 missense variant G/A snv 0.010 1.000 1 2001 2001
dbSNP: rs1023934247
rs1023934247
1 1.000 0.120 10 70598292 missense variant G/C;T snv 0.010 1.000 1 2008 2008
dbSNP: rs10272724
rs10272724
4 0.882 0.200 7 50409515 downstream gene variant T/C snv 0.24 0.010 < 0.001 1 2011 2011
dbSNP: rs10336
rs10336
4 0.851 0.240 4 76001835 3 prime UTR variant A/G;T snv 0.010 1.000 1 2009 2009
dbSNP: rs1041740
rs1041740
8 0.807 0.320 21 31667849 intron variant C/T snv 0.24 0.010 1.000 1 2018 2018
dbSNP: rs1042713
rs1042713
63 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.010 1.000 1 2008 2008
dbSNP: rs1048990
rs1048990
8 0.790 0.280 14 35292469 5 prime UTR variant C/G;T snv 0.19; 4.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs1055271
rs1055271
1 1.000 0.120 22 50489911 3 prime UTR variant G/C snv 0.27 0.010 1.000 1 2011 2011
dbSNP: rs1063856
rs1063856
VWF
14 0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 0.010 1.000 1 2000 2000
dbSNP: rs10741657
rs10741657
34 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 0.010 < 0.001 1 2007 2007
dbSNP: rs10766196
rs10766196
2 0.925 0.120 11 14891585 5 prime UTR variant A/G snv 0.35 0.010 1.000 1 2019 2019
dbSNP: rs10770125
rs10770125
4 0.882 0.200 11 2147784 missense variant A/G snv 0.49 0.40 0.010 1.000 1 2013 2013
dbSNP: rs10811661
rs10811661
22 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 0.010 1.000 1 2012 2012
dbSNP: rs10889677
rs10889677
40 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 0.010 < 0.001 1 2013 2013
dbSNP: rs10914542
rs10914542
LCK
2 0.925 0.120 1 32262639 intron variant C/G snv 0.15 0.010 1.000 1 2019 2019
dbSNP: rs10918706
rs10918706
2 0.925 0.200 1 167496884 intron variant C/T snv 0.24 0.010 1.000 1 2015 2015
dbSNP: rs11014284
rs11014284
2 0.925 0.240 10 18451155 intron variant T/G snv 0.20 0.010 1.000 1 2019 2019
dbSNP: rs11074932
rs11074932
1 1.000 0.120 16 10874479 intron variant T/A;C snv 0.010 1.000 1 2012 2012
dbSNP: rs11170466
rs11170466
1 1.000 0.120 12 53192075 3 prime UTR variant C/T snv 5.8E-02 0.010 1.000 1 2014 2014
dbSNP: rs11171806
rs11171806
7 0.807 0.360 12 56339747 synonymous variant G/A snv 4.9E-02 4.5E-02 0.010 1.000 1 2013 2013
dbSNP: rs11209026
rs11209026
46 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 < 0.001 1 2013 2013