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: rs2237892
rs2237892
2 0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 0.900 1.000 6 2008 2019
dbSNP: rs2237895
rs2237895
1 0.790 0.240 11 2835964 intron variant A/C;T snv 0.900 0.889 2 2008 2019
dbSNP: rs2237897
rs2237897
2 0.882 0.200 11 2837316 intron variant C/T snv 8.1E-02 0.880 1.000 3 2008 2019
dbSNP: rs231362
rs231362
1 1.000 0.080 11 2670241 non coding transcript exon variant A/G snv 0.62 0.840 1.000 3 2010 2019
dbSNP: rs163184
rs163184
1 1.000 0.080 11 2825839 intron variant T/G snv 0.40 0.810 1.000 4 2010 2018
dbSNP: rs2237896
rs2237896
1 1.000 0.080 11 2837210 intron variant G/A;T snv 0.810 1.000 3 2011 2019
dbSNP: rs163177
rs163177
1 1.000 0.080 11 2817183 intron variant T/C snv 0.45 0.810 1.000 1 2010 2017
dbSNP: rs163182
rs163182
1 0.882 0.160 11 2822986 intron variant G/A;C snv 0.810 1.000 1 2011 2016
dbSNP: rs231361
rs231361
1 1.000 0.080 11 2670270 non coding transcript exon variant G/A snv 0.31 0.800 1.000 1 2012 2012
dbSNP: rs8181588
rs8181588
1 1.000 0.080 11 2810311 intron variant T/C snv 0.12 0.800 1.000 1 2014 2014
dbSNP: rs2283228
rs2283228
1 1.000 0.080 11 2828300 intron variant A/C snv 0.10 0.760 1.000 2 2009 2017
dbSNP: rs117601636
rs117601636
1 1.000 0.080 11 2620807 non coding transcript exon variant A/G snv 5.5E-03 0.700 1.000 1 2016 2016
dbSNP: rs231356
rs231356
1 0.925 0.080 11 2684113 non coding transcript exon variant A/G;T snv 0.700 1.000 1 2014 2014
dbSNP: rs233449
rs233449
1 1.000 0.080 11 2822573 intron variant G/A snv 0.22 0.700 1.000 1 2019 2019
dbSNP: rs76868685
rs76868685
1 1.000 0.080 11 2836784 intron variant C/G snv 2.3E-04 0.700 1.000 1 2019 2019
dbSNP: rs77402029
rs77402029
1 1.000 0.080 11 2619190 non coding transcript exon variant G/A;T snv 0.700 1.000 1 2019 2019