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: rs907092
rs907092
3 0.925 0.080 17 39766006 synonymous variant G/A snv 0.41 0.36 0.810 1.000 5 2010 2019
dbSNP: rs9303277
rs9303277
9 0.790 0.240 17 39820216 intron variant C/T snv 0.52 0.720 1.000 4 2010 2017
dbSNP: rs3816470
rs3816470
3 0.925 0.160 17 39829548 intron variant A/G snv 0.54 0.710 1.000 2 2011 2015
dbSNP: rs10445308
rs10445308
5 0.851 0.240 17 39781794 intron variant C/T snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs12450323
rs12450323
2 0.925 0.120 17 39816455 intron variant G/T snv 0.18 0.700 1.000 1 2014 2014
dbSNP: rs2313430
rs2313430
2 0.925 0.160 17 39773563 intron variant T/C snv 0.48 0.700 1.000 1 2011 2011
dbSNP: rs9909593
rs9909593
3 0.925 0.160 17 39813896 intron variant A/G snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs1453559
rs1453559
2 0.925 0.160 17 39864166 5 prime UTR variant T/C snv 0.47 0.52 0.010 1.000 1 2012 2012
dbSNP: rs9635726
rs9635726
2 0.925 0.160 17 39863888 intron variant C/T snv 0.18 0.010 1.000 1 2013 2013