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: rs5882
rs5882
35 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 0.020 1.000 2 1999 2012
dbSNP: rs17231520
rs17231520
9 0.851 0.240 16 56961915 upstream gene variant G/A snv 2.1E-02 0.010 1.000 1 2015 2015
dbSNP: rs1800777
rs1800777
17 0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 0.010 1.000 1 2001 2001
dbSNP: rs569033466
rs569033466
6 0.882 0.160 16 56961929 5 prime UTR variant G/A;C;T snv 4.8E-05; 2.4E-05 0.010 1.000 1 2015 2015