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: rs1011939
rs1011939
1 16 19981674 intergenic variant G/A snv 0.59 0.700 1.000 1 2016 2016
dbSNP: rs1012167
rs1012167
1 20 40530479 intergenic variant T/C snv 0.49 0.700 1.000 1 2019 2019
dbSNP: rs10147938
rs10147938
1 14 31416745 intron variant C/T snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs10173538
rs10173538
5 2 159712765 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10181515
rs10181515
1 2 226154745 TF binding site variant C/T snv 0.26 0.700 1.000 1 2019 2019
dbSNP: rs10221267
rs10221267
1 17 70468521 intergenic variant C/T snv 0.57 0.700 1.000 1 2019 2019
dbSNP: rs10265057
rs10265057
1 7 47236139 intergenic variant A/G snv 0.15 0.700 1.000 1 2019 2019
dbSNP: rs10265133
rs10265133
1 7 45856005 downstream gene variant G/T snv 0.12 0.700 1.000 1 2019 2019
dbSNP: rs10283100
rs10283100
3 8 119583783 missense variant A/G;T snv 0.96 0.700 1.000 1 2019 2019
dbSNP: rs10402712
rs10402712
1 19 33435107 intron variant G/A snv 0.30 0.700 1.000 1 2016 2016
dbSNP: rs1042725
rs1042725
7 0.882 0.080 12 65964567 3 prime UTR variant C/T snv 0.48 0.800 1.000 1 2013 2013
dbSNP: rs10437653
rs10437653
1 11 46276080 upstream gene variant A/C snv 0.57 0.700 1.000 1 2019 2019
dbSNP: rs10495563
rs10495563
1 2 9522081 3 prime UTR variant G/A;C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10509669
rs10509669
1 10 94210156 intron variant A/T snv 0.22 0.700 1.000 1 2019 2019
dbSNP: rs10734564
rs10734564
1 11 48138877 intron variant A/G snv 0.74 0.700 1.000 1 2019 2019
dbSNP: rs10788038
rs10788038
1 10 120117008 intergenic variant T/C snv 0.61 0.700 1.000 1 2007 2007
dbSNP: rs10814916
rs10814916
7 0.851 0.200 9 4293150 intron variant A/C snv 0.57 0.700 1.000 1 2019 2019
dbSNP: rs10830963
rs10830963
27 0.776 0.400 11 92975544 intron variant C/G snv 0.22 0.700 1.000 3 2016 2019
dbSNP: rs10872678
rs10872678
1 6 151718829 intron variant T/C snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs10883846
rs10883846
1 10 103198487 intergenic variant C/T snv 0.31 0.700 1.000 1 2019 2019
dbSNP: rs10895278
rs10895278
1 11 102224604 intron variant T/C snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs10913200
rs10913200
1 1 176552519 intron variant G/A snv 1.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs10935733
rs10935733
1 3 148905181 intron variant T/C snv 0.52 0.700 1.000 2 2016 2019
dbSNP: rs10985827
rs10985827
1 9 122939329 non coding transcript exon variant T/G snv 0.34 0.700 1.000 1 2019 2019
dbSNP: rs1101081
rs1101081
1 6 151711782 intron variant C/T snv 0.26 0.700 1.000 1 2016 2016