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: rs16955379
rs16955379
1 1.000 0.080 16 81455768 intron variant C/T snv 3.6E-02 0.810 1.000 1 2011 2019
dbSNP: rs2925979
rs2925979
10 1.000 0.080 16 81501185 intron variant T/A;C snv 0.710 1.000 3 2017 2018
dbSNP: rs12596103
rs12596103
1 1.000 0.080 16 81456948 intron variant C/T snv 1.4E-02 0.700 1.000 1 2011 2011