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: rs1333040
rs1333040
15 0.732 0.280 9 22083405 intron variant C/G;T snv 0.840 1.000 6 2008 2015
dbSNP: rs10757272
rs10757272
6 0.851 0.160 9 22088261 intron variant C/T snv 0.41 0.820 1.000 2 2012 2019
dbSNP: rs6475606
rs6475606
5 0.882 0.080 9 22081851 intron variant C/T snv 0.62 0.810 1.000 1 2012 2012
dbSNP: rs10733376
rs10733376
3 1.000 0.080 9 22114470 intron variant G/C snv 0.64 0.710 1.000 1 2014 2014
dbSNP: rs2383207
rs2383207
22 0.695 0.280 9 22115960 intron variant A/G snv 0.64 0.700 1.000 1 2010 2010
dbSNP: rs7866503
rs7866503
3 0.882 0.080 9 22091925 intron variant G/T snv 0.50 0.700 1.000 1 2016 2016
dbSNP: rs10757278
rs10757278
44 0.620 0.520 9 22124478 intron variant A/G snv 0.40 0.030 0.667 3 2008 2014
dbSNP: rs496892
rs496892
6 0.827 0.160 9 22024352 intron variant C/T snv 0.40 0.010 < 0.001 1 2010 2010