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: rs894160
rs894160
4 0.882 0.120 15 89668592 intron variant C/T snv 0.29 0.040 1.000 4 2008 2013
dbSNP: rs2289487
rs2289487
1 1.000 0.080 15 89673865 intron variant C/T snv 0.54 0.020 1.000 2 2008 2016
dbSNP: rs6496589
rs6496589
1 1.000 0.080 15 89669998 missense variant G/C;T snv 0.93; 4.1E-06 0.010 1.000 1 2015 2015
dbSNP: rs8179043
rs8179043
1 1.000 0.080 15 89668913 intron variant T/C snv 0.58 0.010 1.000 1 2008 2008