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: rs2416257
rs2416257
1 0.882 0.160 5 111099792 intron variant C/G;T snv 0.800 1.000 1 2009 2009
dbSNP: rs10045577
rs10045577
1 5 111090753 intron variant C/A;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs55905691
rs55905691
2 5 111090287 intron variant A/G snv 0.13 0.700 1.000 1 2016 2016
dbSNP: rs79881201
rs79881201
2 5 111092097 5 prime UTR variant C/T snv 0.26 0.700 1.000 1 2016 2016