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: rs10181656
rs10181656
9 0.763 0.360 2 191105153 intron variant G/C snv 0.79 0.020 1.000 2 2012 2017
dbSNP: rs10865331
rs10865331
5 0.827 0.120 2 62324337 intergenic variant A/G snv 0.57 0.700 1.000 1 2019 2019
dbSNP: rs10888503
rs10888503
2 0.925 0.080 1 152621073 downstream gene variant C/T snv 0.59 0.010 1.000 1 2015 2015
dbSNP: rs11171806
rs11171806
7 0.807 0.360 12 56339747 synonymous variant G/A snv 4.9E-02 4.5E-02 0.010 1.000 1 2013 2013
dbSNP: rs11209026
rs11209026
46 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.040 1.000 4 2008 2019
dbSNP: rs114212579
rs114212579
1 1.000 0.080 6 31968280 non coding transcript exon variant G/T snv 0.700 1.000 1 2019 2019
dbSNP: rs114265779
rs114265779
1 1.000 0.080 6 30213844 upstream gene variant C/T snv 0.700 1.000 1 2019 2019
dbSNP: rs114383947
rs114383947
1 1.000 0.080 6 31010940 intron variant C/T snv 0.700 1.000 1 2019 2019
dbSNP: rs114598684
rs114598684
1 1.000 0.080 6 31413173 intron variant C/T snv 0.700 1.000 1 2019 2019
dbSNP: rs114757170
rs114757170
1 1.000 0.080 6 30618254 intron variant G/A snv 0.700 1.000 1 2019 2019
dbSNP: rs115112280
rs115112280
1 1.000 0.080 6 32390772 non coding transcript exon variant T/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs115145466
rs115145466
1 1.000 0.080 6 32251264 upstream gene variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs115429782
rs115429782
1 1.000 0.080 6 31297975 intron variant T/C snv 0.700 1.000 1 2019 2019
dbSNP: rs115429849
rs115429849
1 1.000 0.080 6 30416827 intron variant G/A snv 0.700 1.000 1 2019 2019
dbSNP: rs115529844
rs115529844
1 1.000 0.080 6 29850244 non coding transcript exon variant C/T snv 0.700 1.000 1 2019 2019
dbSNP: rs115618145
rs115618145
1 1.000 0.080 6 30102498 upstream gene variant C/G snv 0.700 1.000 1 2019 2019
dbSNP: rs115645848
rs115645848
1 1.000 0.080 6 29622938 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs115872194
rs115872194
1 1.000 0.080 6 31639897 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs115928623
rs115928623
1 1.000 0.080 6 29971371 intron variant A/T snv 0.700 1.000 1 2019 2019
dbSNP: rs116199901
rs116199901
1 1.000 0.080 6 30315875 intron variant G/C snv 0.700 1.000 1 2019 2019
dbSNP: rs116340302
rs116340302
1 1.000 0.080 6 31528604 non coding transcript exon variant A/T snv 0.700 1.000 1 2019 2019
dbSNP: rs116805908
rs116805908
1 1.000 0.080 6 31173746 non coding transcript exon variant C/T snv 0.700 1.000 1 2019 2019
dbSNP: rs12044149
rs12044149
2 0.925 0.080 1 67135003 intron variant G/C;T snv 0.710 1.000 1 2015 2015
dbSNP: rs12188300
rs12188300
6 0.807 0.120 5 159402519 intron variant A/G;T snv 0.800 1.000 1 2010 2010
dbSNP: rs12189871
rs12189871
2 0.925 0.080 6 31284147 intron variant C/T snv 8.6E-02 0.010 1.000 1 2015 2015