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: rs11138902
rs11138902
1 9 69488398 intron variant G/A;T snv 0.700 1.000 4 2017 2019
dbSNP: rs13010010
rs13010010
1 2 100236272 intron variant C/T snv 0.27 0.700 1.000 4 2017 2019
dbSNP: rs17814604
rs17814604
1 6 98137626 intron variant A/G snv 0.19 0.700 1.000 4 2017 2019
dbSNP: rs34305371
rs34305371
1 1 72267927 intron variant G/A snv 6.6E-02 0.700 1.000 4 2017 2019
dbSNP: rs9384679
rs9384679
1 6 108543216 intron variant C/T snv 0.46 0.700 1.000 4 2017 2019
dbSNP: rs10733389
rs10733389
1 9 23378222 intron variant A/C;G;T snv 0.700 1.000 3 2018 2019
dbSNP: rs10858096
rs10858096
1 1 109424482 intron variant C/A snv 0.43 0.700 1.000 3 2018 2019
dbSNP: rs11191270
rs11191270
1 10 102364848 intron variant C/T snv 0.16 0.700 1.000 3 2018 2019
dbSNP: rs11210871
rs11210871
1 1 43563682 intron variant C/A;G;T snv 0.700 1.000 3 2018 2019
dbSNP: rs12025777
rs12025777
1 1 41283225 intron variant G/T snv 8.3E-02 0.700 1.000 3 2018 2019
dbSNP: rs12441495
rs12441495
1 15 40930289 non coding transcript exon variant G/C snv 8.2E-02 0.700 1.000 3 2018 2019
dbSNP: rs12707116
rs12707116
1 7 133740156 intron variant T/C snv 0.48 0.700 1.000 3 2017 2019
dbSNP: rs12744310
rs12744310
1 1 41307830 intron variant C/T snv 0.18 0.700 1.000 3 2017 2019
dbSNP: rs12885221
rs12885221
1 14 32809804 intron variant G/A;C snv 0.700 1.000 3 2018 2019
dbSNP: rs13105581
rs13105581
1 4 102307673 intron variant C/T snv 9.0E-02 0.700 1.000 3 2018 2019
dbSNP: rs13425585
rs13425585
1 2 156630761 intergenic variant C/G snv 0.51 0.700 1.000 3 2017 2019
dbSNP: rs17589603
rs17589603
1 1 72167202 intron variant A/G snv 7.4E-02 0.700 1.000 3 2018 2019
dbSNP: rs1933720
rs1933720
1 6 97849956 intron variant T/C snv 0.26 0.700 1.000 3 2018 2019
dbSNP: rs2289328
rs2289328
IVD
1 15 40413218 intron variant G/A snv 0.12 0.700 1.000 3 2017 2019
dbSNP: rs2295499
rs2295499
1 4 2715963 intron variant C/T snv 0.44 0.700 1.000 3 2017 2019
dbSNP: rs2426132
rs2426132
1 20 49106590 intergenic variant G/C snv 0.47 0.700 1.000 3 2017 2019
dbSNP: rs2624839
rs2624839
1 3 50164798 intron variant T/C snv 0.48 0.700 1.000 3 2018 2019
dbSNP: rs2721173
rs2721173
1 8 144519045 intron variant C/T snv 0.43 0.700 1.000 3 2017 2019
dbSNP: rs310333
rs310333
1 16 71545764 intron variant A/C snv 0.71 0.700 1.000 3 2018 2019
dbSNP: rs34172651
rs34172651
1 16 24755520 intron variant T/C snv 0.35 0.700 1.000 3 2018 2019