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: rs16986921
rs16986921
3 1.000 0.080 20 37754119 intron variant C/T snv 0.12 0.700 1.000 1 2008 2008
dbSNP: rs6013029
rs6013029
5 0.882 0.160 20 37771178 intron variant G/T snv 0.12 0.700 1.000 1 2008 2008
dbSNP: rs6020712
rs6020712
4 1.000 0.080 20 37758210 intron variant G/A snv 0.12 0.700 1.000 1 2008 2008