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: rs11761352
rs11761352
2 7 55883254 upstream gene variant C/A snv 0.23 0.700 1.000 1 2019 2019
dbSNP: rs11766051
rs11766051
2 7 55770852 intron variant G/A;C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs12613336
rs12613336
6 2 210704675 regulatory region variant T/C snv 0.19 0.700 1.000 1 2019 2019
dbSNP: rs12671091
rs12671091
2 7 55950973 intron variant T/C snv 0.44 0.700 1.000 1 2019 2019
dbSNP: rs13244654
rs13244654
4 7 56079263 intron variant T/C snv 0.48 0.700 1.000 1 2019 2019
dbSNP: rs1744297
rs1744297
12 14 104102135 intron variant T/C snv 0.86 0.700 1.000 1 2019 2019
dbSNP: rs2135116
rs2135116
2 7 55923451 non coding transcript exon variant A/G snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs2242508
rs2242508
2 7 56083796 intron variant A/G snv 0.49 0.700 1.000 1 2019 2019
dbSNP: rs2538054
rs2538054
2 7 56142748 intergenic variant A/G snv 0.17 0.700 1.000 1 2019 2019
dbSNP: rs34148685
rs34148685
2 7 56156046 intergenic variant T/C snv 4.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs35210477
rs35210477
2 7 56044524 intron variant A/G snv 4.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs4535700
rs4535700
2 7 55977755 intron variant T/C snv 0.72 0.700 1.000 1 2019 2019
dbSNP: rs4948106
rs4948106
2 7 56099902 downstream gene variant T/G snv 0.53 0.700 1.000 1 2019 2019
dbSNP: rs6966061
rs6966061
2 7 55781097 intergenic variant A/G snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs7782243
rs7782243
2 7 56114152 downstream gene variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs7793921
rs7793921
3 7 56053188 intron variant G/A snv 0.64 0.700 1.000 1 2019 2019
dbSNP: rs816396
rs816396
2 7 56169587 intergenic variant T/C snv 0.18 0.700 1.000 1 2019 2019
dbSNP: rs816411
rs816411
3 1.000 0.040 7 56103796 intron variant C/T snv 0.53 0.700 1.000 1 2019 2019