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: rs4765913
rs4765913
1 1.000 0.040 12 2310730 intron variant A/T snv 0.82 0.810 1.000 4 2011 2017
dbSNP: rs10896135
rs10896135
1 1.000 0.040 11 66783531 intron variant G/A;C snv 0.800 1.000 2 2011 2018
dbSNP: rs11013860
rs11013860
1 1.000 0.040 10 18365098 intron variant A/C;G snv 0.11 0.020 1.000 2 2014 2019
dbSNP: rs12899449
rs12899449
1 1.000 0.040 15 38703290 intron variant A/G snv 0.24 0.800 1.000 2 2008 2011
dbSNP: rs1487441
rs1487441
1 1.000 0.040 6 98106018 intron variant G/A snv 0.39 0.800 1.000 2 2014 2016
dbSNP: rs17138171
rs17138171
1 1.000 0.040 11 79351885 intron variant T/A;C snv 0.700 1.000 2 2013 2014
dbSNP: rs1944449
rs1944449
1 1.000 0.040 11 79372205 intron variant C/T snv 0.18 0.700 1.000 2 2013 2014
dbSNP: rs2302417
rs2302417
1 1.000 0.040 3 52780240 non coding transcript exon variant T/A snv 0.44; 3.1E-03; 1.5E-04; 1.0E-05 0.42 0.700 1.000 2 2017 2019
dbSNP: rs4789
rs4789
1 1.000 0.040 3 36827948 3 prime UTR variant T/C snv 0.44 0.700 1.000 2 2013 2014
dbSNP: rs9525580
rs9525580
1 1.000 0.040 13 42146563 intron variant G/A snv 0.23 0.020 1.000 2 2016 2019
dbSNP: rs10035291
rs10035291
1 1.000 0.040 5 81500549 intron variant T/C snv 0.46 0.700 1.000 1 2019 2019
dbSNP: rs1012053
rs1012053
1 1.000 0.040 13 42079301 intron variant C/A snv 0.85 0.800 1.000 1 2008 2008
dbSNP: rs10134944
rs10134944
1 1.000 0.040 14 57652478 intron variant C/T snv 0.13 0.800 1.000 1 2011 2011
dbSNP: rs10168049
rs10168049
1 1.000 0.040 2 121320830 intergenic variant A/G snv 0.16 0.710 1.000 1 2019 2019
dbSNP: rs10455979
rs10455979
1 1.000 0.040 6 166581772 intron variant C/A;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10459221
rs10459221
1 1.000 0.040 12 49073211 upstream gene variant C/A;G snv 0.700 1.000 1 2017 2017
dbSNP: rs10488140
rs10488140
1 1.000 0.040 7 55070695 intron variant C/T snv 0.26 0.700 1.000 1 2008 2008
dbSNP: rs10489167
rs10489167
1 1.000 0.040 1 40710794 intron variant G/A snv 0.13 0.700 1.000 1 2016 2016
dbSNP: rs10501439
rs10501439
1 1.000 0.040 11 79374802 intron variant A/G snv 0.18 0.700 1.000 1 2014 2014
dbSNP: rs10509129
rs10509129
1 1.000 0.040 10 60311283 intron variant G/A;T snv 0.700 1.000 1 2014 2014
dbSNP: rs10511083
rs10511083
1 1.000 0.040 3 85521809 intron variant A/G snv 0.51 0.700 1.000 1 2013 2013
dbSNP: rs10512928
rs10512928
1 1.000 0.040 5 7546298 intron variant C/T snv 0.15 0.700 1.000 1 2014 2014
dbSNP: rs10513249
rs10513249
1 1.000 0.040 9 114541631 intergenic variant C/A;G snv 0.700 1.000 1 2016 2016
dbSNP: rs1051375
rs1051375
1 1.000 0.040 12 2679713 synonymous variant G/A snv 0.68 0.57 0.010 1.000 1 2013 2013
dbSNP: rs10761473
rs10761473
1 1.000 0.040 10 60300624 intron variant C/G snv 0.12 0.700 1.000 1 2014 2014