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: rs16921209
rs16921209
3 0.882 0.160 10 20879174 intron variant C/G snv 4.6E-02 0.710 1.000 1 2016 2016
dbSNP: rs7922552
rs7922552
2 0.925 0.160 10 20896095 intron variant C/G;T snv 0.010 1.000 1 2016 2016