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: rs26528
rs26528
9 0.807 0.200 16 28506388 intron variant T/C snv 0.43 0.010 1.000 1 2017 2017
dbSNP: rs2857656
rs2857656
5 0.851 0.120 17 34254988 upstream gene variant G/A;C snv 0.010 1.000 1 2009 2009
dbSNP: rs35385902
rs35385902
9 0.807 0.240 4 99347122 missense variant C/A;T snv 2.0E-05; 1.1E-03 0.010 1.000 1 2007 2007
dbSNP: rs3869109
rs3869109
5 0.851 0.160 6 31216419 intergenic variant A/G;T snv 0.010 1.000 1 2013 2013
dbSNP: rs40837
rs40837
5 0.925 0.120 16 28499524 3 prime UTR variant A/G snv 0.43 0.010 1.000 1 2017 2017
dbSNP: rs5361
rs5361
47 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 0.010 1.000 1 2003 2003
dbSNP: rs5882
rs5882
35 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 0.010 1.000 1 2016 2016
dbSNP: rs5888
rs5888
11 0.752 0.200 12 124800202 synonymous variant A/G;T snv 0.59; 4.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs646776
rs646776
25 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.010 1.000 1 2019 2019
dbSNP: rs659366
rs659366
17 0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 0.010 1.000 1 2019 2019
dbSNP: rs660339
rs660339
24 0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43 0.010 1.000 1 2019 2019
dbSNP: rs662
rs662
157 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 0.010 1.000 1 2007 2007
dbSNP: rs7044343
rs7044343
13 0.752 0.520 9 6254208 intron variant C/T snv 0.51 0.010 1.000 1 2017 2017
dbSNP: rs738409
rs738409
88 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 0.010 1.000 1 2017 2017
dbSNP: rs761646500
rs761646500
3 0.925 0.080 6 169237763 missense variant C/G snv 4.0E-06 0.010 1.000 1 2002 2002
dbSNP: rs777659543
rs777659543
6 0.882 0.120 11 74006231 missense variant G/A snv 4.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs9282541
rs9282541
13 0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 0.010 1.000 1 2012 2012
dbSNP: rs9349379
rs9349379
19 0.732 0.200 6 12903725 intron variant A/G snv 0.32 0.010 1.000 1 2016 2016