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: rs11078927
rs11078927
3 0.925 0.080 17 39908152 intron variant C/T snv 0.40 0.35 0.010 1.000 1 2013 2013
dbSNP: rs2305480
rs2305480
10 0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 0.010 1.000 1 2013 2013
dbSNP: rs7216389
rs7216389
14 0.732 0.440 17 39913696 intron variant C/T snv 0.60 0.010 1.000 1 2012 2012