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: rs10075801
rs10075801
5 5 132341949 intron variant A/G snv 0.31 0.700 1.000 1 2016 2016
dbSNP: rs10086568
rs10086568
2 1.000 0.120 8 7042814 upstream gene variant G/A snv 0.34 0.700 1.000 1 2016 2016
dbSNP: rs10100356
rs10100356
1 8 129613918 intron variant G/A snv 0.22 0.700 1.000 1 2018 2018
dbSNP: rs10138752
rs10138752
5 14 68713254 intron variant C/T snv 8.8E-02 0.700 1.000 1 2016 2016
dbSNP: rs10165200
rs10165200
2 2 8299499 intron variant G/A snv 0.36 0.700 1.000 1 2016 2016
dbSNP: rs10173538
rs10173538
5 2 159712765 intron variant C/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1025688
rs1025688
3 18 50621506 intron variant G/A snv 0.35 0.700 1.000 1 2016 2016
dbSNP: rs10265538
rs10265538
2 7 20502242 intergenic variant T/C snv 0.20 0.700 1.000 1 2016 2016
dbSNP: rs10283564
rs10283564
2 9 5075628 intron variant C/G snv 0.23 0.700 1.000 1 2016 2016
dbSNP: rs1032726
rs1032726
2 3 112967228 intron variant T/C snv 0.46 0.700 1.000 1 2016 2016
dbSNP: rs1036207
rs1036207
3 1.000 0.080 5 142119476 intron variant A/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1036332
rs1036332
3 1 199043349 intron variant A/C snv 0.70 0.700 1.000 1 2016 2016
dbSNP: rs10401672
rs10401672
1 19 33269055 regulatory region variant C/T snv 0.30 0.700 1.000 1 2016 2016
dbSNP: rs10409243
rs10409243
6 19 10222312 3 prime UTR variant C/A;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs10410864
rs10410864
2 19 39711776 downstream gene variant T/C snv 0.68 0.700 1.000 1 2016 2016
dbSNP: rs10542411
rs10542411
2 2 61541105 upstream gene variant ATATT/-;ATATTATATT delins 0.23 0.700 1.000 1 2016 2016
dbSNP: rs1057258
rs1057258
3 2 233206983 3 prime UTR variant C/T snv 0.30 0.700 1.000 1 2016 2016
dbSNP: rs1059513
rs1059513
11 0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 0.700 1.000 1 2016 2016
dbSNP: rs10667251
rs10667251
4 0.925 0.080 17 49388381 intron variant -/TCT delins 0.47 0.700 1.000 1 2016 2016
dbSNP: rs10795656
rs10795656
4 1.000 0.080 10 8553876 intergenic variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs10852622
rs10852622
2 16 88490472 intron variant A/G snv 0.35 0.700 1.000 1 2016 2016
dbSNP: rs10858740
rs10858740
5 12 88451258 intergenic variant A/G;T snv 0.56 0.700 1.000 1 2016 2016
dbSNP: rs10893844
rs10893844
2 11 128315955 regulatory region variant G/C snv 0.36 0.700 1.000 1 2016 2016
dbSNP: rs10995240
rs10995240
2 10 62628871 intron variant G/C snv 0.29 0.700 1.000 1 2016 2016
dbSNP: rs11065979
rs11065979
12 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 0.700 1.000 1 2016 2016