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: rs10012
rs10012
16 0.716 0.280 2 38075247 missense variant G/C snv 0.31 0.36 0.020 1.000 2 2012 2017
dbSNP: rs1002481
rs1002481
3 0.882 0.080 6 111390819 intron variant T/A;G snv 0.010 1.000 1 2013 2013
dbSNP: rs10036653
rs10036653
4 0.851 0.160 5 81970563 upstream gene variant A/T snv 0.17 0.010 1.000 1 2017 2017
dbSNP: rs10040363
rs10040363
3 0.882 0.080 5 83177826 intron variant A/G snv 0.50 0.010 1.000 1 2011 2011
dbSNP: rs10053847
rs10053847
3 0.882 0.080 5 35878038 3 prime UTR variant G/A snv 0.13 0.010 1.000 1 2019 2019
dbSNP: rs10054203
rs10054203
3 0.882 0.080 5 1279849 intron variant G/A;C;T snv 0.010 1.000 1 2019 2019
dbSNP: rs10069690
rs10069690
53 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.010 1.000 1 2017 2017
dbSNP: rs10079250
rs10079250
7 0.827 0.120 5 150070569 missense variant T/C snv 9.9E-02 8.6E-02 0.020 1.000 2 2014 2017
dbSNP: rs1014264982
rs1014264982
3 0.882 0.080 19 3577038 missense variant G/A;C snv 6.8E-06 7.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs10187911
rs10187911
3 0.882 0.080 2 50420809 intron variant C/A;G;T snv 0.010 1.000 1 2013 2013
dbSNP: rs1019340046
rs1019340046
5 0.882 0.080 17 7674225 missense variant C/T snv 0.010 < 0.001 1 1993 1993
dbSNP: rs10213865
rs10213865
5 0.827 0.120 5 35857748 intron variant A/C;T snv 0.010 1.000 1 2019 2019
dbSNP: rs10244817
rs10244817
3 0.882 0.080 7 124827416 intron variant T/C snv 0.22 0.010 1.000 1 2009 2009
dbSNP: rs10254120
rs10254120
5 0.851 0.080 7 6005996 missense variant C/A;G;T snv 7.2E-02 0.010 1.000 1 2014 2014
dbSNP: rs1026411
rs1026411
5 0.827 0.080 8 127014165 intron variant G/A;C snv 0.25 0.010 1.000 1 2019 2019
dbSNP: rs1035938
rs1035938
8 0.776 0.120 19 47680514 missense variant C/G;T snv 0.29 0.010 1.000 1 2018 2018
dbSNP: rs10412613
rs10412613
3 0.882 0.080 19 52209575 intron variant G/A snv 0.63 0.010 1.000 1 2017 2017
dbSNP: rs1041983
rs1041983
15 0.732 0.240 8 18400285 synonymous variant C/T snv 0.34 0.36 0.010 1.000 1 2015 2015
dbSNP: rs1042028
rs1042028
30 0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 0.040 0.750 4 2004 2012
dbSNP: rs10421768
rs10421768
6 0.807 0.120 19 35281996 intron variant A/G snv 0.21 0.010 1.000 1 2019 2019
dbSNP: rs1042522
rs1042522
242 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.100 0.850 20 2000 2018
dbSNP: rs1042711
rs1042711
5 0.827 0.120 5 148826785 5 prime UTR variant C/A;G;T snv 4.2E-06; 0.68 0.010 1.000 1 2019 2019
dbSNP: rs1043973338
rs1043973338
3 0.882 0.080 2 112830483 missense variant A/C snv 0.010 1.000 1 2007 2007
dbSNP: rs1043994
rs1043994
7 0.827 0.120 19 15192033 synonymous variant T/A;C snv 4.0E-06; 0.85 0.010 1.000 1 2019 2019
dbSNP: rs1044396
rs1044396
17 0.742 0.240 20 63349782 missense variant G/A;C snv 0.47; 6.1E-05 0.010 1.000 1 2020 2020