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: rs2200733
rs2200733
12 0.752 0.240 4 110789013 intergenic variant C/T snv 0.18 0.030 1.000 3 2008 2013
dbSNP: rs10033464
rs10033464
8 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 0.010 1.000 1 2013 2013
dbSNP: rs13143308
rs13143308
4 0.882 0.120 4 110793263 upstream gene variant T/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs16939239
rs16939239
1 1.000 8 76122993 intergenic variant G/A snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs1906591
rs1906591
5 0.851 0.200 4 110787733 intergenic variant G/A snv 0.15 0.010 1.000 1 2014 2014
dbSNP: rs635634
rs635634
22 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs638704
rs638704
1 1.000 1 170629046 intron variant C/T snv 0.64 0.700 1.000 1 2018 2018
dbSNP: rs6891174
rs6891174
2 0.925 0.040 5 173213587 intergenic variant A/G snv 0.73 0.700 1.000 1 2018 2018
dbSNP: rs505922
rs505922
ABO
34 0.689 0.520 9 133273813 intron variant C/T snv 0.010 < 0.001 1 2013 2013
dbSNP: rs2257073
rs2257073
1 1.000 7 151186200 intron variant C/T snv 0.26 0.010 1.000 1 2015 2015
dbSNP: rs4727833
rs4727833
1 1.000 7 116507854 3 prime UTR variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs5065
rs5065
12 0.763 0.240 1 11846011 stop lost A/G snv 0.14 0.21 0.010 1.000 1 2012 2012
dbSNP: rs5067
rs5067
2 0.925 0.080 1 11845924 3 prime UTR variant A/G;T snv 0.21 0.010 1.000 1 2012 2012
dbSNP: rs1205
rs1205
CRP
46 0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 0.010 1.000 1 2015 2015
dbSNP: rs4444878
rs4444878
7 0.851 0.120 4 186292729 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs761740955
rs761740955
FGB
5 0.827 0.200 4 154566637 missense variant A/G snv 4.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs11596587
rs11596587
HK1
1 1.000 10 69354232 intron variant C/T snv 0.11 0.700 1.000 1 2018 2018
dbSNP: rs1217691063
rs1217691063
614 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs2273235
rs2273235
1 1.000 5 150527971 synonymous variant T/G snv 0.45 0.42 0.010 1.000 1 2019 2019
dbSNP: rs74154533
rs74154533
1 1.000 10 103547967 intron variant G/A snv 0.17 0.700 1.000 1 2018 2018
dbSNP: rs1800779
rs1800779
9 0.763 0.320 7 150992855 intron variant G/A;C snv 0.010 1.000 1 2015 2015
dbSNP: rs2910829
rs2910829
3 0.925 0.080 5 60174072 intron variant G/A snv 0.52 0.010 1.000 1 2006 2006
dbSNP: rs152312
rs152312
3 0.925 0.080 5 60491989 non coding transcript exon variant G/A;T snv 0.020 1.000 2 2006 2011
dbSNP: rs20417
rs20417
57 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2015 2015
dbSNP: rs146390073
rs146390073
1 1.000 1 241142948 intron variant C/T snv 1.1E-02 0.700 1.000 1 2018 2018