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: rs1883025
rs1883025
13 0.807 0.120 9 104902020 intron variant C/T snv 0.28 0.800 1.000 1 2012 2012
dbSNP: rs12686004
rs12686004
6 1.000 0.040 9 104891145 intron variant G/A snv 9.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs3905000
rs3905000
5 0.925 0.080 9 104894789 intron variant G/A snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs9282541
rs9282541
13 0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 0.020 0.500 2 2008 2015