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: rs864745
rs864745
12 0.763 0.320 7 28140937 intron variant T/C snv 0.41 0.020 1.000 2 2009 2013
dbSNP: rs10486567
rs10486567
9 0.851 0.120 7 27936944 intron variant G/A snv 0.28 0.010 < 0.001 1 2010 2010
dbSNP: rs6968704
rs6968704
4 0.882 0.120 7 27927365 intron variant C/T snv 0.35 0.010 < 0.001 1 2010 2010