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: rs11079454
rs11079454
3 0.882 0.080 17 61679808 3 prime UTR variant T/A;C snv 0.020 0.500 2 2013 2016
dbSNP: rs3117027
rs3117027
3 0.882 0.080 6 33121846 intron variant C/A;G snv 0.020 1.000 2 2014 2018
dbSNP: rs9272143
rs9272143
3 0.882 0.080 6 32633026 intron variant T/C snv 0.49 0.020 1.000 2 2014 2014
dbSNP: rs1003897973
rs1003897973
3 0.882 0.080 19 6746039 missense variant C/G snv 0.010 < 0.001 1 2002 2002
dbSNP: rs1030389
rs1030389
3 0.882 0.080 15 25032641 non coding transcript exon variant A/G snv 0.41 0.010 1.000 1 2016 2016
dbSNP: rs10426502
rs10426502
3 0.882 0.080 19 4651257 intron variant G/A snv 6.8E-02 0.010 1.000 1 2019 2019
dbSNP: rs1045935
rs1045935
3 0.882 0.080 15 25036439 non coding transcript exon variant G/A;T snv 0.010 1.000 1 2016 2016
dbSNP: rs1048512
rs1048512
3 0.882 0.080 1 160025108 3 prime UTR variant G/A;T snv 0.13 0.010 1.000 1 2016 2016
dbSNP: rs1060555
rs1060555
3 0.882 0.080 19 4652810 3 prime UTR variant C/G;T snv 0.010 1.000 1 2019 2019
dbSNP: rs10815144
rs10815144
3 0.882 0.080 9 5010192 intron variant G/A snv 0.62 0.010 1.000 1 2014 2014
dbSNP: rs11202058
rs11202058
3 0.882 0.080 10 86522854 non coding transcript exon variant G/A snv 0.25 0.010 1.000 1 2015 2015
dbSNP: rs1195571
rs1195571
3 0.882 0.080 12 130739483 intergenic variant T/C snv 0.97 0.010 < 0.001 1 2019 2019
dbSNP: rs12349785
rs12349785
3 0.882 0.080 9 5076613 intron variant G/C snv 0.23 0.010 1.000 1 2014 2014
dbSNP: rs12646659
rs12646659
3 0.882 0.080 4 176764117 intron variant C/G snv 5.4E-02 0.010 1.000 1 2019 2019
dbSNP: rs16945692
rs16945692
3 0.882 0.080 17 61862883 intron variant A/G snv 0.17 0.010 1.000 1 2013 2013
dbSNP: rs17885289
rs17885289
3 0.882 0.080 10 44386212 non coding transcript exon variant C/T snv 0.26 0.010 1.000 1 2009 2009
dbSNP: rs180082
rs180082
3 0.882 0.080 17 69955727 intergenic variant C/G;T snv 0.010 < 0.001 1 2013 2013
dbSNP: rs266093
rs266093
3 0.882 0.080 10 44370760 3 prime UTR variant C/G;T snv 0.010 1.000 1 2009 2009
dbSNP: rs2732044
rs2732044
3 0.882 0.080 15 25032169 non coding transcript exon variant G/A snv 0.34 0.010 1.000 1 2016 2016
dbSNP: rs281860374
rs281860374
3 0.882 0.080 6 31271730 missense variant G/C snv 0.010 < 0.001 1 2002 2002
dbSNP: rs2862833
rs2862833
FAS
3 0.882 0.080 10 89015872 3 prime UTR variant A/G snv 0.45 0.010 1.000 1 2016 2016
dbSNP: rs300574
rs300574
3 0.882 0.080 4 123402583 3 prime UTR variant T/C snv 0.58 0.54 0.010 1.000 1 2016 2016
dbSNP: rs3094
rs3094
3 0.882 0.080 14 20699896 3 prime UTR variant T/C snv 0.18 0.010 1.000 1 2017 2017
dbSNP: rs3213172
rs3213172
3 0.882 0.080 20 33677511 missense variant C/T snv 2.4E-05 2.1E-05 0.010 1.000 1 2018 2018
dbSNP: rs3744935
rs3744935
3 0.882 0.080 18 63127447 3 prime UTR variant C/T snv 6.0E-03 0.010 1.000 1 2016 2016