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: rs11142238
rs11142238
1 1.000 0.040 9 88310479 TF binding site variant A/C snv 0.20 0.700 1.000 1 2017 2017
dbSNP: rs11200391
rs11200391
1 1.000 0.040 10 122091346 intron variant A/C snv 0.47 0.700 1.000 1 2017 2017
dbSNP: rs11255590
rs11255590
1 1.000 0.040 10 5858325 downstream gene variant A/C snv 7.5E-02 0.700 1.000 1 2017 2017
dbSNP: rs11610288
rs11610288
1 1.000 0.040 12 115742549 intergenic variant A/C snv 7.0E-02 0.700 1.000 1 2017 2017
dbSNP: rs11629474
rs11629474
1 1.000 0.040 15 77771243 intron variant A/C snv 0.19 0.700 1.000 1 2017 2017
dbSNP: rs11666940
rs11666940
1 1.000 0.040 19 17972400 intron variant A/C snv 0.12 0.700 1.000 1 2017 2017
dbSNP: rs11699092
rs11699092
1 1.000 0.040 20 40856047 upstream gene variant A/C snv 0.10 0.700 1.000 1 2017 2017
dbSNP: rs11720123
rs11720123
1 1.000 0.040 3 57709286 regulatory region variant A/C snv 0.82 0.700 1.000 1 2017 2017
dbSNP: rs11789719
rs11789719
1 1.000 0.040 9 33304803 intron variant A/C snv 6.0E-02 0.700 1.000 1 2017 2017
dbSNP: rs11883614
rs11883614
1 1.000 0.040 2 38290346 downstream gene variant A/C snv 0.32 0.700 1.000 1 2017 2017
dbSNP: rs11888257
rs11888257
1 1.000 0.040 2 16989772 intergenic variant A/C snv 0.28 0.700 1.000 1 2017 2017
dbSNP: rs11891602
rs11891602
1 1.000 0.040 2 118666722 regulatory region variant A/C snv 9.2E-02 0.700 1.000 1 2017 2017
dbSNP: rs1193096
rs1193096
1 1.000 0.040 1 208022171 downstream gene variant A/C snv 0.93 0.700 1.000 1 2017 2017
dbSNP: rs11959743
rs11959743
1 1.000 0.040 5 25947289 intergenic variant A/C snv 0.17 0.700 1.000 1 2017 2017
dbSNP: rs11972102
rs11972102
1 1.000 0.040 7 51433548 intergenic variant A/C snv 0.67 0.700 1.000 1 2017 2017
dbSNP: rs11998250
rs11998250
1 1.000 0.040 8 3162070 intron variant A/C snv 0.22 0.700 1.000 1 2017 2017
dbSNP: rs12032770
rs12032770
1 1.000 0.040 1 29868950 intergenic variant A/C snv 0.93 0.700 1.000 1 2017 2017
dbSNP: rs1213640
rs1213640
1 1.000 0.040 1 58328345 intron variant A/C snv 0.77 0.700 1.000 1 2017 2017
dbSNP: rs12401392
rs12401392
1 1.000 0.040 1 101430389 intergenic variant A/C snv 9.1E-02 0.700 1.000 1 2017 2017
dbSNP: rs12410473
rs12410473
1 1.000 0.040 1 209064125 regulatory region variant A/C snv 0.14 0.700 1.000 1 2017 2017
dbSNP: rs12537318
rs12537318
1 1.000 0.040 7 125996951 intergenic variant A/C snv 0.75 0.700 1.000 1 2017 2017
dbSNP: rs12570130
rs12570130
1 1.000 0.040 10 71072964 intron variant A/C snv 6.6E-02 0.700 1.000 1 2017 2017
dbSNP: rs12574551
rs12574551
1 1.000 0.040 11 75630017 intron variant A/C snv 4.9E-02 0.700 1.000 1 2017 2017
dbSNP: rs12618289
rs12618289
1 1.000 0.040 2 83702324 intergenic variant A/C snv 0.59 0.700 1.000 1 2017 2017
dbSNP: rs12712018
rs12712018
1 1.000 0.040 2 108237049 regulatory region variant A/C snv 0.32 0.700 1.000 1 2017 2017