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: rs1415259
rs1415259
5 0.925 0.080 1 162115519 intron variant C/T snv 0.54 0.010 1.000 1 2015 2015
dbSNP: rs1858232
rs1858232
4 0.882 0.080 1 162334048 intron variant A/G;T snv 0.010 1.000 1 2015 2015
dbSNP: rs386231
rs386231
4 0.882 0.080 1 162356033 intron variant C/T snv 0.68 0.010 1.000 1 2013 2013
dbSNP: rs6704393
rs6704393
3 0.925 0.080 1 162182266 intron variant C/A;T snv 0.010 1.000 1 2015 2015