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: rs10822407
rs10822407
1 10 65024342 intergenic variant T/C snv 0.30 0.700 1.000 1 2016 2016
dbSNP: rs10850519
rs10850519
1 12 115490635 intergenic variant G/C snv 0.22 0.700 1.000 1 2017 2017
dbSNP: rs10864859
rs10864859
1 2 120682642 downstream gene variant G/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10873612
rs10873612
1 15 25860455 intron variant C/T snv 0.45 0.700 1.000 1 2018 2018
dbSNP: rs10906391
rs10906391
1 10 13481937 intron variant C/T snv 0.28 0.700 1.000 1 2018 2018
dbSNP: rs10916082
rs10916082
1 1 227064925 intron variant A/G snv 0.30 0.700 1.000 1 2017 2017
dbSNP: rs10920250
rs10920250
1 1 201755384 intron variant G/A snv 0.24 0.700 1.000 1 2019 2019
dbSNP: rs10926991
rs10926991
1 1 243329265 intron variant A/G snv 0.30 0.700 1.000 1 2019 2019
dbSNP: rs10943605
rs10943605
1 6 78945760 3 prime UTR variant G/A snv 0.44 0.700 1.000 1 2016 2016
dbSNP: rs1098708
rs1098708
1 12 27168179 intergenic variant A/G snv 0.35 0.700 1.000 1 2018 2018
dbSNP: rs11022734
rs11022734
1 11 13260033 intergenic variant A/G snv 0.64 0.700 1.000 1 2018 2018
dbSNP: rs11026586
rs11026586
1 11 22493987 intron variant G/A;T snv 8.3E-02 0.700 1.000 1 2018 2018
dbSNP: rs11044990
rs11044990
1 12 20019998 intron variant A/G snv 0.12 0.700 1.000 1 2018 2018
dbSNP: rs11108209
rs11108209
1 12 95716077 intron variant T/C snv 7.0E-02 0.700 1.000 1 2018 2018
dbSNP: rs111304266
rs111304266
1 5 57293715 intergenic variant C/G snv 2.7E-02 0.700 1.000 1 2017 2017
dbSNP: rs11141731
rs11141731
1 9 87273557 intergenic variant C/T snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs111447985
rs111447985
1 10 103918153 5 prime UTR variant C/A;T snv 1.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs111630016
rs111630016
1 7 158255704 intron variant C/T snv 3.8E-02 0.700 1.000 1 2017 2017
dbSNP: rs111770209
rs111770209
1 2 164677837 intron variant T/C snv 1.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs111777102
rs111777102
1 10 110206068 upstream gene variant C/T snv 5.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs112140754
rs112140754
1 6 156924099 intron variant T/C snv 3.6E-03 0.700 1.000 1 2018 2018
dbSNP: rs113134141
rs113134141
1 3 46820449 intergenic variant A/G snv 0.17 0.700 1.000 1 2018 2018
dbSNP: rs114334738
rs114334738
1 9 28165673 intron variant T/C snv 1.5E-02 0.700 1.000 1 2017 2017
dbSNP: rs114503346
rs114503346
1 5 172765347 intron variant C/T snv 2.7E-02 0.700 1.000 1 2018 2018
dbSNP: rs11466111
rs11466111
1 1 115286557 missense variant C/T snv 1.0E-02 1.2E-02 0.700 1.000 1 2017 2017