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: rs1127313
rs1127313
1 1.000 0.120 1 154583949 3 prime UTR variant G/A snv 0.41 0.010 1.000 1 2016 2016
dbSNP: rs633862
rs633862
5 0.925 0.120 9 133279871 upstream gene variant T/C snv 0.49 0.020 1.000 2 2014 2017
dbSNP: rs10017134
rs10017134
2 0.925 0.120 4 69591303 intron variant T/C snv 0.75 0.010 1.000 1 2019 2019
dbSNP: rs1002076
rs1002076
2 0.925 0.120 1 10378834 3 prime UTR variant G/A snv 0.33 0.010 < 0.001 1 2015 2015
dbSNP: rs1017134
rs1017134
2 0.925 0.120 7 35307237 intergenic variant G/A snv 0.47 0.010 1.000 1 2019 2019
dbSNP: rs1057156
rs1057156
2 0.925 0.120 3 128081228 3 prime UTR variant A/G snv 0.22 0.23 0.010 1.000 1 2019 2019
dbSNP: rs10788679
rs10788679
2 0.925 0.120 1 17590467 intron variant A/G snv 0.59 0.010 1.000 1 2018 2018
dbSNP: rs11175194
rs11175194
2 0.925 0.120 12 63871057 intron variant G/A snv 0.15 0.010 1.000 1 2014 2014
dbSNP: rs114972508
rs114972508
2 0.925 0.120 7 55020815 intron variant T/C snv 1.4E-02 0.010 1.000 1 2019 2019
dbSNP: rs11696662
rs11696662
2 0.925 0.120 20 41161795 intron variant C/T snv 4.4E-02 0.010 1.000 1 2014 2014
dbSNP: rs1192691
rs1192691
2 0.925 0.120 10 36880367 regulatory region variant G/T snv 0.90 0.010 1.000 1 2014 2014
dbSNP: rs1413299
rs1413299
2 0.925 0.120 9 98998959 intron variant G/A;T snv 0.010 1.000 1 2014 2014
dbSNP: rs142091544
rs142091544
2 0.925 0.120 5 168286995 upstream gene variant C/T snv 2.1E-02 0.010 1.000 1 2019 2019
dbSNP: rs146314922
rs146314922
2 0.925 0.120 19 54982828 missense variant A/G snv 0.010 1.000 1 2005 2005
dbSNP: rs149652370
rs149652370
2 0.925 0.120 3 128084115 non coding transcript exon variant A/G snv 1.3E-04 0.010 1.000 1 2019 2019
dbSNP: rs1596797
rs1596797
2 0.925 0.120 19 8977341 missense variant T/A;C;G snv 2.0E-05; 4.0E-06; 0.74 0.010 < 0.001 1 2011 2011
dbSNP: rs1649942
rs1649942
3 0.925 0.120 10 82191935 intron variant G/A;C snv 0.010 1.000 1 2019 2019
dbSNP: rs17106154
rs17106154
2 0.925 0.120 14 68694457 non coding transcript exon variant T/C snv 7.8E-02 0.010 1.000 1 2014 2014
dbSNP: rs17250239
rs17250239
2 0.925 0.120 9 136902178 non coding transcript exon variant G/A snv 7.2E-02 0.010 1.000 1 2014 2014
dbSNP: rs17329882
rs17329882
2 0.925 0.120 4 119028805 intron variant A/C;T snv 0.010 1.000 1 2017 2017
dbSNP: rs17427875
rs17427875
2 0.925 0.120 7 27185939 non coding transcript exon variant A/T snv 0.15 0.010 1.000 1 2015 2015
dbSNP: rs17507066
rs17507066
2 0.925 0.120 22 28696732 intron variant C/T snv 7.0E-02 0.010 1.000 1 2015 2015
dbSNP: rs17702471
rs17702471
2 0.925 0.120 13 93224864 upstream gene variant A/G snv 0.16 0.010 1.000 1 2015 2015
dbSNP: rs1955513
rs1955513
2 0.925 0.120 14 32706736 intron variant T/G snv 0.11 0.010 1.000 1 2018 2018
dbSNP: rs1983383
rs1983383
2 0.925 0.120 2 30754766 intron variant C/A snv 0.39 0.010 1.000 1 2015 2015