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: rs1048943
rs1048943
88 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.050 1.000 5 2003 2019
dbSNP: rs1799814
rs1799814
8 0.807 0.160 15 74720646 missense variant G/A;T snv 1.6E-05; 3.1E-02 0.010 1.000 1 2005 2005
dbSNP: rs368952331
rs368952331
4 0.925 0.080 15 74722805 missense variant C/T snv 2.8E-05 6.3E-05 0.010 < 0.001 1 2010 2010