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: rs5498
rs5498
2 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 0.700 1.000 1 2018 2018
dbSNP: rs75407602
rs75407602
1 19 10286554 3 prime UTR variant C/T snv 3.1E-02 0.700 1.000 1 2018 2018