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: rs55916943
rs55916943
1 1.000 0.080 X 106313139 intergenic variant G/A snv 0.11 0.700 1.000 1 2018 2018
dbSNP: rs138520829
rs138520829
1 1.000 0.080 X 106504267 intergenic variant T/C snv 5.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs10465287
rs10465287
1 1.000 0.080 X 106545130 intergenic variant T/A;G snv 0.700 1.000 1 2018 2018
dbSNP: rs149055315
rs149055315
1 1.000 0.080 X 106730962 intron variant T/A snv 5.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs66491909
rs66491909
1 1.000 0.080 X 106732269 intron variant G/A snv 0.21 0.700 1.000 1 2018 2018
dbSNP: rs148655558
rs148655558
1 1.000 0.080 X 106768355 intron variant T/G snv 0.700 1.000 1 2018 2018
dbSNP: rs76047242
rs76047242
1 1.000 0.080 X 106816683 intron variant C/T snv 2.5E-02 0.700 1.000 1 2018 2018
dbSNP: rs62605968
rs62605968
1 1.000 0.080 X 106829297 3 prime UTR variant T/C snv 0.41 0.700 1.000 1 2018 2018
dbSNP: rs34689332
rs34689332
1 1.000 0.080 X 106834287 intron variant G/A snv 5.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs5962770
rs5962770
1 1.000 0.080 X 106893680 intron variant T/C snv 0.22 0.700 1.000 1 2018 2018
dbSNP: rs7057398
rs7057398
5 0.827 0.080 X 106901299 intron variant T/C snv 0.41 0.710 1.000 2 2015 2018
dbSNP: rs12008279
rs12008279
3 0.882 0.080 X 106917472 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs12014762
rs12014762
3 0.882 0.080 X 106940440 intron variant C/T snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs6622126
rs6622126
4 0.851 0.080 X 106956972 missense variant G/A snv 0.58 0.700 1.000 1 2018 2018
dbSNP: rs141052845
rs141052845
1 1.000 0.080 X 106964394 intron variant A/G snv 5.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs11092578
rs11092578
1 1.000 0.080 X 106983213 intron variant C/T snv 0.17 0.700 1.000 1 2018 2018
dbSNP: rs12688220
rs12688220
5 0.827 0.200 X 107001537 upstream gene variant C/T snv 0.19 0.010 1.000 1 2015 2015
dbSNP: rs1298993
rs1298993
1 1.000 0.080 X 107043226 regulatory region variant G/A snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs1285582
rs1285582
1 1.000 0.080 X 107123872 3 prime UTR variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs12688091
rs12688091
1 1.000 0.080 X 107131628 intron variant G/A snv 0.23 0.700 1.000 1 2018 2018
dbSNP: rs1285594
rs1285594
1 1.000 0.080 X 107158099 intron variant G/C snv 0.700 1.000 1 2018 2018
dbSNP: rs12847061
rs12847061
1 1.000 0.080 X 107230661 intron variant C/T snv 5.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs12857658
rs12857658
1 1.000 0.080 X 107281285 intergenic variant G/A snv 5.0E-02 0.700 1.000 1 2018 2018
dbSNP: rs6622208
rs6622208
1 1.000 0.080 X 107289163 intergenic variant G/C snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs148771016
rs148771016
1 1.000 0.080 X 107318205 intergenic variant A/C snv 5.1E-02 0.700 1.000 1 2018 2018