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: rs1039049
rs1039049
1 1.000 0.040 4 80416472 intron variant G/A snv 0.98 0.700 1.000 1 2015 2015
dbSNP: rs1041536
rs1041536
1 1.000 0.040 20 9907627 intergenic variant T/C snv 0.46 0.700 1.000 1 2015 2015
dbSNP: rs111231532
rs111231532
1 1.000 0.040 3 39135911 intron variant C/T snv 5.0E-02 0.700 1.000 1 2015 2015
dbSNP: rs111600634
rs111600634
1 1.000 0.040 9 117856347 intron variant T/G snv 1.5E-02 0.700 1.000 1 2015 2015
dbSNP: rs112961612
rs112961612
1 1.000 0.040 20 41872026 intergenic variant T/A snv 8.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs113793030
rs113793030
1 1.000 0.040 10 70287104 upstream gene variant T/C snv 1.7E-02 0.700 1.000 1 2015 2015
dbSNP: rs115199861
rs115199861
1 1.000 0.040 1 171670879 non coding transcript exon variant C/G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs115700680
rs115700680
1 1.000 0.040 1 171381070 intergenic variant T/G snv 1.9E-02 0.700 1.000 1 2015 2015
dbSNP: rs115764752
rs115764752
1 1.000 0.040 1 171778066 upstream gene variant T/C snv 7.9E-03 0.700 1.000 1 2015 2015
dbSNP: rs116065238
rs116065238
1 1.000 0.040 1 171482283 upstream gene variant A/G snv 4.3E-03 0.700 1.000 1 2015 2015
dbSNP: rs116237496
rs116237496
1 1.000 0.040 8 101033687 upstream gene variant T/C snv 4.0E-02 0.700 1.000 1 2015 2015
dbSNP: rs117070989
rs117070989
1 1.000 0.040 6 137490510 downstream gene variant C/A snv 8.3E-03 0.700 1.000 1 2015 2015
dbSNP: rs117129097
rs117129097
1 1.000 0.040 12 128054737 intron variant C/G;T snv 1.9E-03 0.010 1.000 1 2019 2019
dbSNP: rs117224174
rs117224174
1 1.000 0.040 6 114654261 intergenic variant G/A snv 2.2E-02 0.700 1.000 1 2015 2015
dbSNP: rs117529438
rs117529438
1 1.000 0.040 12 64979216 intron variant C/T snv 3.4E-02 0.700 1.000 1 2019 2019
dbSNP: rs117605016
rs117605016
1 1.000 0.040 12 129129840 intron variant C/A snv 9.9E-03 0.700 1.000 1 2015 2015
dbSNP: rs117932393
rs117932393
1 1.000 0.040 9 106390428 intron variant C/T snv 8.4E-03 0.700 1.000 1 2015 2015
dbSNP: rs1216578110
rs1216578110
APP
1 1.000 0.040 21 25955652 missense variant T/C snv 4.0E-06 7.0E-06 0.010 1.000 1 2018 2018
dbSNP: rs12230170
rs12230170
1 1.000 0.040 12 128762838 intergenic variant T/A;G snv 0.700 1.000 1 2015 2015
dbSNP: rs12435940
rs12435940
1 1.000 0.040 14 25552779 intergenic variant A/G snv 0.97 0.700 1.000 1 2015 2015
dbSNP: rs12468965
rs12468965
1 1.000 0.040 2 53528621 downstream gene variant G/A snv 1.8E-02 0.700 1.000 1 2015 2015
dbSNP: rs12624302
rs12624302
1 1.000 0.040 2 3168181 regulatory region variant T/C snv 3.0E-02 0.700 1.000 1 2015 2015
dbSNP: rs12628463
rs12628463
1 1.000 0.040 22 19401286 intron variant C/A snv 6.2E-03 0.700 1.000 1 2015 2015
dbSNP: rs1264499143
rs1264499143
1 1.000 0.040 16 681593 missense variant G/A snv 4.1E-06 0.010 1.000 1 2014 2014
dbSNP: rs13133980
rs13133980
1 1.000 0.040 4 41000929 intron variant G/A;C;T snv 0.010 1.000 1 2013 2013