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: rs2049045
rs2049045
3 1.000 0.080 11 27672694 intron variant G/A;C snv 0.13 0.700 1.000 1 2017 2017
dbSNP: rs4923460
rs4923460
3 11 27635242 intron variant G/T snv 0.20 0.700 1.000 1 2017 2017
dbSNP: rs7103411
rs7103411
15 0.752 0.160 11 27678578 intron variant C/T snv 0.82 0.700 1.000 1 2017 2017