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: rs25409
rs25409
4 0.882 0.080 15 26773694 missense variant G/A snv 2.9E-03 3.5E-03 0.020 1.000 2 2008 2011
dbSNP: rs4906902
rs4906902
14 0.724 0.200 15 26774621 intron variant A/G snv 0.15 0.020 < 0.001 2 2007 2012
dbSNP: rs71651682
rs71651682
3 0.925 0.040 15 26772759 missense variant C/T snv 0.020 1.000 2 2008 2012