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: rs6785358
rs6785358
4 0.882 0.200 3 30602723 upstream gene variant G/A snv 0.84 0.010 1.000 1 2015 2015
dbSNP: rs746800707
rs746800707
8 0.851 0.160 20 36240388 missense variant G/A;C;T snv 1.2E-05; 4.0E-06 0.700 0
dbSNP: rs1045642
rs1045642
214 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.010 1.000 1 2014 2014
dbSNP: rs755246809
rs755246809
7 0.827 0.280 6 135404951 frameshift variant T/- delins 5.9E-04 4.9E-05 0.700 0
dbSNP: rs1557612048
rs1557612048
11 0.807 0.200 1 26767868 missense variant T/C snv 0.700 0
dbSNP: rs1565569158
rs1565569158
4 12 6939148 missense variant A/G snv 0.700 0
dbSNP: rs1701
rs1701
1 17 81402198 non coding transcript exon variant C/A;G;T snv 0.010 1.000 1 2013 2013
dbSNP: rs180177039
rs180177039
12 0.851 0.160 7 140778006 missense variant T/A;C;G snv 0.700 0
dbSNP: rs113331868
rs113331868
6 5 150228191 splice donor variant C/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs759125480
rs759125480
16 0.827 0.160 5 123377409 stop gained G/A snv 1.6E-05 0.700 0
dbSNP: rs1383180
rs1383180
1 4 5783715 missense variant G/A;T snv 0.35; 2.4E-05 0.010 1.000 1 2018 2018
dbSNP: rs2164331
rs2164331
1 2 135910326 intron variant C/T snv 0.18 0.010 1.000 1 2016 2016
dbSNP: rs309143
rs309143
1 2 135956608 intron variant A/G snv 0.19 0.010 1.000 1 2016 2016
dbSNP: rs6738266
rs6738266
1 2 135985602 5 prime UTR variant C/T snv 2.8E-02 2.8E-02 0.010 1.000 1 2016 2016
dbSNP: rs1555564126
rs1555564126
9 0.882 0.320 17 44853306 frameshift variant C/- delins 0.700 0
dbSNP: rs1555565774
rs1555565774
16 0.807 0.360 17 44862753 frameshift variant G/- delins 0.700 0
dbSNP: rs755273705
rs755273705
EVC
1 4 5729349 missense variant C/G;T snv 2.0E-05 0.010 1.000 1 2018 2018
dbSNP: rs1057518868
rs1057518868
3 0.925 0.080 16 86510849 missense variant A/T snv 0.700 0
dbSNP: rs1114167294
rs1114167294
4 0.925 6 41587455 frameshift variant T/- del 0.700 0
dbSNP: rs61729366
rs61729366
6 0.851 0.240 4 78511299 missense variant G/A snv 5.2E-03 5.8E-03 0.700 0
dbSNP: rs143044921
rs143044921
8 0.827 0.280 13 38691375 missense variant G/A;T snv 3.5E-03 0.700 0
dbSNP: rs104894073
rs104894073
8 0.827 0.080 8 11750213 missense variant G/A;C;T snv 0.020 1.000 2 2011 2012
dbSNP: rs56208331
rs56208331
4 0.925 0.080 8 11758419 missense variant G/A;T snv 2.0E-03 0.020 0.500 2 2009 2010
dbSNP: rs1185861796
rs1185861796
2 1.000 0.080 8 11758339 missense variant C/A snv 8.0E-06 7.0E-06 0.010 1.000 1 2018 2018
dbSNP: rs146017816
rs146017816
2 1.000 8 11758471 missense variant C/G;T snv 7.2E-05; 1.6E-05 0.010 1.000 1 2009 2009