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: rs1938492
rs1938492
3 1 65652146 intergenic variant A/C snv 0.43 0.800 1.000 1 2013 2013
dbSNP: rs2106854
rs2106854
3 5 132433482 intron variant C/T snv 0.23 0.800 1.000 1 2013 2013
dbSNP: rs2286503
rs2286503
3 7 22816987 intron variant C/T snv 0.48 0.800 1.000 1 2013 2013
dbSNP: rs2522056
rs2522056
4 5 132466034 intron variant G/A snv 0.25 0.800 1.000 1 2009 2009
dbSNP: rs434943
rs434943
3 14 68847342 intergenic variant G/A snv 0.27 0.800 1.000 1 2013 2013
dbSNP: rs511154
rs511154
3 3 136232079 intergenic variant A/G;T snv 0.800 1.000 1 2009 2009
dbSNP: rs6050
rs6050
FGA
10 0.827 0.120 4 154586438 missense variant T/A;C snv 0.29 0.800 1.000 1 2011 2011
dbSNP: rs7204230
rs7204230
3 16 53158419 intron variant T/C snv 0.31 0.800 1.000 1 2013 2013
dbSNP: rs7681423
rs7681423
5 4 154621096 intergenic variant C/T snv 0.26 0.800 1.000 1 2011 2011
dbSNP: rs7896783
rs7896783
3 10 63402393 intron variant G/A;C snv 0.800 1.000 1 2013 2013
dbSNP: rs7968440
rs7968440
3 12 50740958 intron variant A/G snv 0.28 0.800 1.000 1 2013 2013
dbSNP: rs1035560
rs1035560
1 16 71998831 intron variant T/A;C snv 0.38 0.700 1.000 2 2016 2017
dbSNP: rs11230201
rs11230201
2 1.000 0.080 11 60229521 intron variant C/G;T snv 0.700 1.000 2 2016 2017
dbSNP: rs1558643
rs1558643
1 2 102115231 intron variant T/C;G snv 0.700 1.000 2 2016 2017
dbSNP: rs1800961
rs1800961
21 0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 0.700 1.000 2 2016 2017
dbSNP: rs1976714
rs1976714
1 3 123145924 intron variant G/T snv 0.32 0.700 1.000 2 2016 2017
dbSNP: rs2228145
rs2228145
57 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.700 1.000 2 2009 2013
dbSNP: rs2710804
rs2710804
3 7 36044919 intron variant T/C snv 0.29 0.700 1.000 2 2016 2017
dbSNP: rs3138493
rs3138493
1 9 89604345 intron variant T/C snv 0.52 0.700 1.000 2 2016 2017
dbSNP: rs59104589
rs59104589
1 2 241298487 intron variant C/T snv 0.30 0.700 1.000 2 2016 2017
dbSNP: rs59950280
rs59950280
4 4 3450618 upstream gene variant G/A snv 0.41 0.700 1.000 2 2016 2017
dbSNP: rs61812598
rs61812598
4 1.000 0.080 1 154447611 intron variant G/A snv 0.31 0.700 1.000 2 2016 2017
dbSNP: rs7012814
rs7012814
2 8 9315848 intron variant G/A;T snv 0.700 1.000 2 2016 2017
dbSNP: rs7224737
rs7224737
3 17 42137346 intron variant G/A snv 0.36 0.700 1.000 2 2016 2017
dbSNP: rs75347843
rs75347843
1 22 50673933 intron variant G/A;C;T snv 0.700 1.000 2 2016 2017