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: rs4430796
rs4430796
14 0.790 0.280 17 37738049 intron variant A/G snv 0.52 0.800 1.000 21 2007 2019
dbSNP: rs7501939
rs7501939
12 0.776 0.280 17 37741165 intron variant C/T snv 0.41 0.740 1.000 8 2008 2018
dbSNP: rs11649743
rs11649743
2 0.925 0.080 17 37714971 intron variant A/G snv 0.85 0.730 1.000 5 2011 2019
dbSNP: rs11651052
rs11651052
7 0.851 0.200 17 37742390 intron variant G/A snv 0.50 0.700 1.000 2 2016 2018
dbSNP: rs11263763
rs11263763
6 0.882 0.200 17 37743574 intron variant A/G snv 0.43 0.700 1.000 1 2015 2015
dbSNP: rs12601991
rs12601991
17 0.708 0.280 17 37741642 intron variant T/A;G snv 0.700 1.000 1 2016 2016
dbSNP: rs2005705
rs2005705
2 0.925 0.120 17 37736310 intron variant G/A snv 0.46 0.700 1.000 1 2014 2014
dbSNP: rs8064454
rs8064454
2 0.925 0.120 17 37741595 intron variant C/A;G snv 0.700 1.000 1 2015 2015
dbSNP: rs3760511
rs3760511
2 0.925 0.080 17 37746322 upstream gene variant G/A;T snv 0.020 1.000 2 2016 2018
dbSNP: rs4794758
rs4794758
2 0.925 0.080 17 37720433 intron variant T/C snv 0.66 0.010 1.000 1 2011 2011
dbSNP: rs757210
rs757210
6 0.807 0.160 17 37736525 intron variant C/G;T snv 0.010 1.000 1 2012 2012