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: rs1314913
rs1314913
6 0.807 0.120 14 68232877 intron variant C/T snv 0.13 0.010 1.000 1 2016 2016
dbSNP: rs2588809
rs2588809
6 0.807 0.160 14 68193711 intron variant T/C snv 0.80 0.010 1.000 1 2016 2016
dbSNP: rs999737
rs999737
8 0.776 0.200 14 68567965 intron variant C/T snv 0.16 0.010 1.000 1 2016 2016