Source: ALL
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: rs7907606
rs7907606 		8 0.790 0.120 10 103920874 upstream gene variant T/G snv 0.26 0.700 1.000 2 2018 2019
dbSNP: rs10508765
rs10508765 		2 1.000 10 31679855 intergenic variant A/G snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs1065827
rs1065827 		1 16 65949614 intergenic variant A/G snv 0.010 1.000 1 2014 2014
dbSNP: rs10835889
rs10835889 		2 1.000 11 32348834 intergenic variant G/A snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs11031731
rs11031731 		3 0.925 0.040 11 32343884 upstream gene variant G/A snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs116251328
rs116251328 		2 1.000 6 34209733 intergenic variant T/A snv 1.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs12224688
rs12224688 		2 1.000 11 32305471 intron variant C/T snv 0.16 0.700 1.000 1 2019 2019
dbSNP: rs12392108
rs12392108 		2 1.000 X 132180234 intergenic variant T/A snv 0.43 0.700 1.000 1 2019 2019
dbSNP: rs12638862
rs12638862 		10 0.827 0.160 3 169759718 downstream gene variant A/G snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs12826786
rs12826786 		26 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 0.010 1.000 1 2019 2019
dbSNP: rs149787529
rs149787529 		2 1.000 4 52165349 intergenic variant C/T snv 0.700 1.000 1 2018 2018
dbSNP: rs2270206
rs2270206 		2 1.000 7 117273513 downstream gene variant C/A snv 0.17 0.700 1.000 1 2019 2019
dbSNP: rs28583837
rs28583837 		2 1.000 12 123379073 upstream gene variant G/A snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs4785384
rs4785384 		2 1.000 16 50114082 intron variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs540409605
rs540409605 		2 1.000 4 45654814 intergenic variant C/G snv 2.1E-03 0.700 1.000 1 2018 2018
dbSNP: rs55768811
rs55768811 		2 1.000 3 5306910 intergenic variant A/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs6094982
rs6094982 		2 1.000 20 48132514 intron variant T/A snv 1.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs61889186
rs61889186 		2 1.000 11 32346024 upstream gene variant C/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs7030354
rs7030354 		2 1.000 9 804231 regulatory region variant C/T snv 0.40 0.700 1.000 1 2018 2018
dbSNP: rs7412010
rs7412010 		2 1.000 1 22109953 regulatory region variant G/C snv 0.14 0.700 1.000 1 2019 2019
dbSNP: rs754058883
rs754058883 		2 1.000 4 45786110 intergenic variant T/C snv 0.700 1.000 1 2018 2018
dbSNP: rs760402913
rs760402913 		2 1.000 4 48948860 regulatory region variant C/T snv 0.700 1.000 1 2018 2018
dbSNP: rs772494879
rs772494879 		2 1.000 4 46136789 intergenic variant C/T snv 0.700 1.000 1 2018 2018
dbSNP: rs775444277
rs775444277 		2 1.000 4 54199163 intron variant C/G snv 0.700 1.000 1 2018 2018
dbSNP: rs779929745
rs779929745 		2 1.000 4 46002240 intergenic variant T/G snv 0.700 1.000 1 2018 2018