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: rs121434500
rs121434500
5 0.851 0.120 20 33410203 missense variant G/A snv 2.0E-05 1.4E-05 0.700 0
dbSNP: rs199473260
rs199473260
2 0.925 0.120 3 38555720 missense variant T/C snv 1.6E-05 3.5E-05 0.700 0
dbSNP: rs13038095
rs13038095
1 1.000 0.080 20 47796832 intergenic variant G/C;T snv 0.800 1.000 1 2010 2010
dbSNP: rs17375901
rs17375901
1 1.000 0.080 1 11792459 intron variant C/T snv 4.6E-02 0.800 1.000 1 2009 2009
dbSNP: rs6666258
rs6666258
3 0.882 0.080 1 154841792 intron variant G/C snv 0.30 0.800 1.000 1 2012 2012
dbSNP: rs10006327
rs10006327
1 1.000 0.080 4 102969823 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs10027347
rs10027347
1 1.000 0.080 4 148025539 intron variant G/T snv 7.7E-02 0.700 1.000 1 2018 2018
dbSNP: rs10165883
rs10165883
1 1.000 0.080 2 69889883 upstream gene variant C/T snv 0.59 0.700 1.000 1 2018 2018
dbSNP: rs10401969
rs10401969
25 0.776 0.240 19 19296909 intron variant T/C snv 0.10 0.700 1.000 1 2016 2016
dbSNP: rs1044258
rs1044258
2 1.000 0.080 10 101845957 3 prime UTR variant T/C snv 0.26 0.700 1.000 1 2018 2018
dbSNP: rs10458660
rs10458660
1 1.000 0.080 10 76176818 intron variant A/G snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs10479177
rs10479177
1 1.000 0.080 5 138052751 upstream gene variant A/G snv 0.30 0.700 1.000 1 2018 2018
dbSNP: rs1049334
rs1049334
6 0.851 0.280 7 116560326 3 prime UTR variant G/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs10741807
rs10741807
1 1.000 0.080 11 19989899 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs10760361
rs10760361
1 1.000 0.080 9 124415987 upstream gene variant G/T snv 0.35 0.700 1.000 1 2018 2018
dbSNP: rs10786662
rs10786662
2 1.000 0.080 10 102230055 downstream gene variant G/C snv 0.58 0.700 1.000 1 2018 2018
dbSNP: rs10800507
rs10800507
1 1.000 0.080 1 170216500 intron variant C/G snv 0.47 0.700 1.000 1 2017 2017
dbSNP: rs10804493
rs10804493
1 1.000 0.080 3 111835579 intron variant G/A snv 0.56 0.700 1.000 1 2018 2018
dbSNP: rs10842383
rs10842383
2 1.000 0.080 12 24619033 intergenic variant C/T snv 0.11 0.700 1.000 1 2018 2018
dbSNP: rs10873298
rs10873298
1 1.000 0.080 14 76960182 non coding transcript exon variant C/T snv 0.46 0.700 1.000 1 2018 2018
dbSNP: rs10873299
rs10873299
1 1.000 0.080 14 76960368 non coding transcript exon variant A/G snv 0.46 0.700 1.000 1 2018 2018
dbSNP: rs11001667
rs11001667
1 1.000 0.080 10 76175587 intron variant A/G snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs11125871
rs11125871
1 1.000 0.080 2 61242991 intron variant C/T snv 0.35 0.700 1.000 1 2018 2018
dbSNP: rs11156751
rs11156751
1 1.000 0.080 14 32521231 intron variant T/C snv 0.27 0.700 1.000 1 2018 2018
dbSNP: rs11180703
rs11180703
1 1.000 0.080 12 75830037 intron variant G/A;T snv 0.700 1.000 1 2018 2018