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: rs4939827
rs4939827
25 0.708 0.160 18 48927093 intron variant T/A;C snv 0.900 0.964 28 2007 2019
dbSNP: rs12953717
rs12953717
18 0.724 0.240 18 48927559 intron variant C/T snv 0.36 0.900 1.000 14 2007 2018
dbSNP: rs7229639
rs7229639
13 0.763 0.080 18 48924606 intron variant A/G snv 0.87 0.820 1.000 6 2014 2019
dbSNP: rs4464148
rs4464148
7 0.827 0.120 18 48932662 intron variant T/C snv 0.25 0.780 1.000 9 2007 2018
dbSNP: rs11874392
rs11874392
11 0.763 0.080 18 48926786 intron variant A/T snv 0.50 0.730 1.000 5 2013 2019
dbSNP: rs7226855
rs7226855
9 0.790 0.080 18 48927678 intron variant A/G;T snv 0.710 1.000 3 2012 2019
dbSNP: rs4939567
rs4939567
9 0.790 0.080 18 48925503 intron variant G/A snv 0.47 0.700 1.000 1 2018 2018
dbSNP: rs6507874
rs6507874
9 0.790 0.080 18 48922435 intron variant T/C snv 0.54 0.700 1.000 1 2018 2018
dbSNP: rs58920878
rs58920878
1 1.000 0.080 18 48923195 intron variant C/A;G;T snv 0.020 1.000 2 2014 2016
dbSNP: rs16950113
rs16950113
1 1.000 0.080 18 48920219 3 prime UTR variant T/C snv 4.7E-02 0.010 1.000 1 2017 2017
dbSNP: rs2337107
rs2337107
3 0.882 0.120 18 48932953 intron variant C/T snv 0.52 0.010 < 0.001 1 2014 2014
dbSNP: rs3764482
rs3764482
3 1.000 0.080 18 48942576 non coding transcript exon variant G/A snv 0.14 0.13 0.010 1.000 1 2017 2017