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: rs1054442
rs1054442
DDN
4 0.925 0.040 12 48995537 3 prime UTR variant A/C snv 0.46 0.700 1.000 4 2017 2019
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: rs2251499
rs2251499
2 1.000 0.040 13 105987507 intron variant T/A;C;G snv 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: rs6801153
rs6801153
2 1.000 0.040 3 24072206 intergenic variant T/C snv 0.74 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: rs10149470
rs10149470
3 1.000 0.040 14 103551616 upstream gene variant A/G snv 0.54 0.700 1.000 3 2017 2019
dbSNP: rs10236197
rs10236197
2 7 32252149 intron variant T/C snv 0.41 0.700 1.000 3 2017 2019
dbSNP: rs10514301
rs10514301
2 5 88643836 intron variant C/T snv 0.16 0.700 1.000 3 2018 2019
dbSNP: rs10733389
rs10733389
1 9 23378222 intron variant A/C;G;T snv 0.700 1.000 3 2018 2019
dbSNP: rs10786662
rs10786662
2 1.000 0.080 10 102230055 downstream gene variant G/C snv 0.58 0.700 1.000 3 2017 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: rs11793831
rs11793831
2 9 23362313 intron variant G/A;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: rs12206087
rs12206087
2 1.000 0.040 6 98135024 intron variant G/A snv 0.39 0.700 1.000 3 2017 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: rs13262595
rs13262595
3 1.000 0.040 8 142235609 intron variant A/C;G snv 0.700 1.000 3 2018 2019