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: rs10512597
rs10512597
4 17 74703694 intron variant T/A;C snv 0.800 1.000 3 2009 2017
dbSNP: rs10157379
rs10157379
3 1 247442297 intron variant C/G;T snv 0.800 1.000 2 2013 2016
dbSNP: rs1035560
rs1035560
1 16 71998831 intron variant T/A;C snv 0.38 0.700 1.000 2 2016 2017
dbSNP: rs11230201
rs11230201
2 1.000 0.080 11 60229521 intron variant C/G;T snv 0.700 1.000 2 2016 2017
dbSNP: rs12239046
rs12239046
9 1 247438293 intron variant T/C snv 0.58 0.800 1.000 2 2011 2017
dbSNP: rs1476698
rs1476698
3 2 241357034 intron variant A/G;T snv 0.800 1.000 2 2013 2017
dbSNP: rs1539019
rs1539019
6 0.882 0.240 1 247436999 intron variant A/C snv 0.63 0.800 1.000 2 2009 2011
dbSNP: rs1558643
rs1558643
1 2 102115231 intron variant T/C;G snv 0.700 1.000 2 2016 2017
dbSNP: rs1976714
rs1976714
1 3 123145924 intron variant G/T snv 0.32 0.700 1.000 2 2016 2017
dbSNP: rs2710804
rs2710804
3 7 36044919 intron variant T/C snv 0.29 0.700 1.000 2 2016 2017
dbSNP: rs3138493
rs3138493
1 9 89604345 intron variant T/C snv 0.52 0.700 1.000 2 2016 2017
dbSNP: rs4129267
rs4129267
13 0.807 0.200 1 154453788 intron variant C/G;T snv 0.800 1.000 2 2011 2013
dbSNP: rs59104589
rs59104589
1 2 241298487 intron variant C/T snv 0.30 0.700 1.000 2 2016 2017
dbSNP: rs61812598
rs61812598
4 1.000 0.080 1 154447611 intron variant G/A snv 0.31 0.700 1.000 2 2016 2017
dbSNP: rs7012814
rs7012814
2 8 9315848 intron variant G/A;T snv 0.700 1.000 2 2016 2017
dbSNP: rs7224737
rs7224737
3 17 42137346 intron variant G/A snv 0.36 0.700 1.000 2 2016 2017
dbSNP: rs7464572
rs7464572
3 8 143946999 intron variant C/A;G snv 0.800 1.000 2 2013 2017
dbSNP: rs75347843
rs75347843
1 22 50673933 intron variant G/A;C;T snv 0.700 1.000 2 2016 2017
dbSNP: rs7916868
rs7916868
3 10 63229171 intron variant A/T snv 0.47 0.700 1.000 2 2016 2017
dbSNP: rs7934094
rs7934094
1 11 43484157 intron variant T/G snv 0.15 0.700 1.000 2 2016 2017
dbSNP: rs1012793
rs1012793
1 5 132445653 intron variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs10489615
rs10489615
3 1 230169242 intron variant A/C;G snv 0.700 1.000 1 2017 2017
dbSNP: rs10519203
rs10519203
8 0.851 0.080 15 78521704 intron variant G/A snv 0.67 0.700 1.000 1 2014 2014
dbSNP: rs10761756
rs10761756
1 10 63412568 intron variant C/T snv 0.42 0.700 1.000 1 2017 2017
dbSNP: rs10864726
rs10864726
1 1 230160406 intron variant C/T snv 0.45 0.700 1.000 1 2017 2017