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: rs139643250
rs139643250
1 19 49013889 intron variant C/T snv 7.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs75287599
rs75287599
1 19 49013883 intron variant C/T snv 7.0E-02 0.700 1.000 1 2018 2018
dbSNP: rs79502742
rs79502742
1 19 48997109 intron variant G/A snv 0.10 0.700 1.000 1 2018 2018
dbSNP: rs79785970
rs79785970
1 19 49014074 intron variant C/G snv 8.0E-02 0.700 1.000 1 2018 2018