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: rs1944449
rs1944449
1 1.000 0.040 11 79372205 intron variant C/T snv 0.18 0.700 1.000 2 2013 2014
dbSNP: rs2075984
rs2075984
3 0.882 0.040 22 38294883 intron variant C/A;G;T snv 0.020 1.000 2 2012 2018
dbSNP: rs2535629
rs2535629
9 0.827 0.040 3 52799203 intron variant G/A;C snv 0.700 1.000 2 2013 2019
dbSNP: rs362719
rs362719
2 0.925 0.040 7 103545430 intron variant C/A snv 0.32 0.020 1.000 2 2010 2011
dbSNP: rs4948418
rs4948418
2 0.925 0.040 10 60425736 intron variant C/T snv 7.9E-02 0.800 1.000 2 2013 2014
dbSNP: rs6295
rs6295
40 0.645 0.200 5 63962738 intron variant C/G snv 0.49 0.020 1.000 2 2011 2013
dbSNP: rs9525580
rs9525580
1 1.000 0.040 13 42146563 intron variant G/A snv 0.23 0.020 1.000 2 2016 2019
dbSNP: rs9525584
rs9525584
2 0.925 0.040 13 42160758 intron variant T/C snv 0.46 0.020 1.000 2 2016 2019
dbSNP: rs994856
rs994856
2 0.925 0.040 13 42134315 intron variant A/G snv 0.37 0.020 1.000 2 2016 2019
dbSNP: rs10035291
rs10035291
1 1.000 0.040 5 81500549 intron variant T/C snv 0.46 0.700 1.000 1 2019 2019
dbSNP: rs10051667
rs10051667
2 0.925 0.080 5 161471322 intron variant T/C snv 0.12 0.010 1.000 1 2015 2015
dbSNP: rs10058613
rs10058613
2 0.925 0.040 5 138358306 intron variant C/A;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1012053
rs1012053
1 1.000 0.040 13 42079301 intron variant C/A snv 0.85 0.800 1.000 1 2008 2008
dbSNP: rs10134944
rs10134944
1 1.000 0.040 14 57652478 intron variant C/T snv 0.13 0.800 1.000 1 2011 2011
dbSNP: rs10275045
rs10275045
5 0.882 0.160 7 1881190 intron variant C/T snv 0.35 0.700 1.000 1 2014 2014
dbSNP: rs1034936
rs1034936
3 0.882 0.080 12 2551994 intron variant C/T snv 0.61 0.010 1.000 1 2020 2020
dbSNP: rs1039002
rs1039002
5 0.851 0.080 6 165741969 intron variant G/A;T snv 0.800 1.000 1 2011 2011
dbSNP: rs10405744
rs10405744
4 0.851 0.040 19 19948684 intron variant G/A snv 9.0E-02 0.700 1.000 1 2015 2015
dbSNP: rs10455979
rs10455979
1 1.000 0.040 6 166581772 intron variant C/A;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10457441
rs10457441
2 1.000 0.040 6 98124244 intron variant T/A;C snv 0.700 1.000 1 2014 2014
dbSNP: rs10488140
rs10488140
1 1.000 0.040 7 55070695 intron variant C/T snv 0.26 0.700 1.000 1 2008 2008
dbSNP: rs10489167
rs10489167
1 1.000 0.040 1 40710794 intron variant G/A snv 0.13 0.700 1.000 1 2016 2016
dbSNP: rs10489744
rs10489744
2 0.925 0.040 1 165411386 intron variant G/A snv 0.55 0.700 1.000 1 2017 2017
dbSNP: rs10494251
rs10494251
4 0.851 0.040 1 147552120 intron variant C/T snv 5.8E-02 0.010 1.000 1 2011 2011
dbSNP: rs10501439
rs10501439
1 1.000 0.040 11 79374802 intron variant A/G snv 0.18 0.700 1.000 1 2014 2014