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: rs10775412
rs10775412
5 0.827 0.120 17 27542007 intron variant A/C snv 0.30 0.700 1.000 1 2016 2016
dbSNP: rs1551399
rs1551399
5 0.827 0.120 8 125527723 intron variant A/C snv 0.46 0.700 1.000 1 2016 2016
dbSNP: rs17780256
rs17780256
6 0.827 0.120 17 72646784 3 prime UTR variant A/C snv 0.18 0.700 1.000 1 2016 2016
dbSNP: rs61802846
rs61802846
5 0.827 0.120 1 161504083 upstream gene variant A/C snv 8.8E-02 0.700 1.000 1 2016 2016
dbSNP: rs79390277
rs79390277
1 1.000 0.040 16 68908687 intron variant A/C snv 3.6E-02 0.700 1.000 1 2017 2017
dbSNP: rs1893592
rs1893592
12 0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 0.700 1.000 2 2016 2017
dbSNP: rs12720356
rs12720356
12 0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs17102823
rs17102823
10 0.776 0.080 14 34894698 intergenic variant A/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs714830
rs714830
5 0.827 0.120 6 20624151 intron variant A/C;G snv 0.13 0.700 1.000 1 2016 2016
dbSNP: rs7195296
rs7195296
5 0.827 0.120 16 11655918 intergenic variant A/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs4672505
rs4672505
5 0.827 0.120 2 62333197 regulatory region variant A/C;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs7426056
rs7426056
6 0.807 0.120 2 203747335 regulatory region variant A/G snv 0.81 0.700 1.000 3 2013 2017
dbSNP: rs3748816
rs3748816
7 0.827 0.200 1 2595307 missense variant A/G snv 0.41 0.46 0.700 1.000 2 2013 2017
dbSNP: rs60652743
rs60652743
2 0.925 0.040 19 46702450 intron variant A/G snv 0.16 0.700 1.000 2 2013 2017
dbSNP: rs10743181
rs10743181
5 0.827 0.120 11 2208529 regulatory region variant A/G snv 0.77 0.700 1.000 1 2016 2016
dbSNP: rs11117431
rs11117431
6 0.807 0.160 16 85981710 intron variant A/G snv 0.18 0.700 1.000 1 2016 2016
dbSNP: rs11632488
rs11632488
1 1.000 0.040 15 79975159 upstream gene variant A/G snv 0.20 0.700 1.000 1 2017 2017
dbSNP: rs11691685
rs11691685
5 0.827 0.120 2 144724260 intron variant A/G snv 5.2E-02 0.700 1.000 1 2016 2016
dbSNP: rs12075255
rs12075255
5 0.827 0.120 1 206788283 intron variant A/G snv 0.74 0.700 1.000 1 2016 2016
dbSNP: rs12694846
rs12694846
5 0.827 0.120 2 230283413 intron variant A/G snv 0.20 0.700 1.000 1 2016 2016
dbSNP: rs13132308
rs13132308
6 0.807 0.160 4 122629959 intron variant A/G snv 0.10 0.700 1.000 1 2016 2016
dbSNP: rs13407913
rs13407913
6 0.827 0.120 2 24874775 intron variant A/G snv 0.54 0.700 1.000 1 2016 2016
dbSNP: rs1452787
rs1452787
5 0.827 0.160 18 55539976 intron variant A/G snv 0.24 0.800 1.000 1 2013 2013
dbSNP: rs1532244
rs1532244
1 1.000 0.040 3 28016414 intron variant A/G snv 0.17 0.700 1.000 1 2018 2018
dbSNP: rs17229679
rs17229679
5 0.827 0.120 2 198696033 intron variant A/G snv 3.0E-02 0.700 1.000 1 2016 2016