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: rs564398
rs564398
18 0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 0.810 1.000 2 2007 2012
dbSNP: rs944801
rs944801
4 0.882 0.120 9 22051671 intron variant G/A;C snv 0.800 1.000 2 2012 2017
dbSNP: rs1063192
rs1063192
24 0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10757274
rs10757274
22 0.701 0.320 9 22096056 intron variant A/G snv 0.41 0.030 1.000 3 2009 2018
dbSNP: rs2383206
rs2383206
17 0.742 0.320 9 22115027 intron variant A/G snv 0.49 0.030 1.000 3 2012 2017
dbSNP: rs10757278
rs10757278
44 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.020 1.000 2 2008 2017
dbSNP: rs1333049
rs1333049
60 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.020 1.000 2 2011 2013
dbSNP: rs2891168
rs2891168
5 0.851 0.160 9 22098620 intron variant A/G snv 0.40 0.020 1.000 2 2009 2010
dbSNP: rs10738610
rs10738610
5 0.882 0.120 9 22123767 intron variant A/C;T snv 0.010 1.000 1 2013 2013
dbSNP: rs1333045
rs1333045
14 0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50 0.010 1.000 1 2018 2018
dbSNP: rs1412829
rs1412829
14 0.742 0.400 9 22043927 intron variant A/G snv 0.28 0.010 1.000 1 2008 2008
dbSNP: rs2383207
rs2383207
22 0.695 0.280 9 22115960 intron variant A/G snv 0.64 0.010 1.000 1 2013 2013
dbSNP: rs495490
rs495490
2 1.000 0.080 9 22010413 intron variant A/G snv 6.8E-02 0.010 1.000 1 2010 2010
dbSNP: rs4977574
rs4977574
26 0.695 0.520 9 22098575 intron variant A/G;T snv 0.010 1.000 1 2013 2013